{"id":219,"date":"2025-04-25T13:12:58","date_gmt":"2025-04-25T04:12:58","guid":{"rendered":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku?page_id=219"},"modified":"2026-04-24T11:43:01","modified_gmt":"2026-04-24T02:43:01","slug":"publication","status":"publish","type":"page","link":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/?page_id=219","title":{"rendered":"Publication"},"content":{"rendered":"<p><span style=\"font-family: tahoma, arial, helvetica, sans-serif\">[2026][<a href=\"#link2025\" class=\"liinternal\">2025<\/a>][<a href=\"#link2024\" class=\"liinternal\">2024<\/a>][<a href=\"#link2023\" class=\"liinternal\">2023<\/a>][<a href=\"#link2022\" class=\"liinternal\">2022<\/a>][<a href=\"#link2021\" class=\"liinternal\">2021<\/a>][<a href=\"#link2020\" class=\"liinternal\">2020<\/a>][<a href=\"#link2019\" class=\"liinternal\">2019<\/a>][<a href=\"#link2018\" class=\"liinternal\">2018<\/a>][<a href=\"#link2017\" class=\"liinternal\">2017<\/a>][<a href=\"#link2016\" class=\"liinternal\">2016<\/a>][<a href=\"#link2015\" class=\"liinternal\">2015<\/a>] [<a href=\"#link2014\" class=\"liinternal\">2014<\/a>] [<a href=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku?page_id=1735\" class=\"liinternal\">2013\u4ee5\u524d<\/a>] <\/span><\/p>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\">2026<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Fujii, T.; Araki, M.; Matsumoto, S.; Ma, B.; Otsuka, T.; Bekker, G.-J.; Kamiya, N.; Ohno, H.; Inuki, S.; Okuno, Y.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Elucidating Ligand Charge Effects in MR1 Cell Surface Translocation Using Molecular Simulations.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>J. Chem. Inf. Model.<\/em>\u00a0<strong>2026<\/strong>,\u00a0<em>66<\/em>, 2211\u20132219.<\/span><\/div>\n<div><a href=\"https:\/\/doi.org\/10.1021\/acs.jcim.5c02141\" class=\"liinternal\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt;color: #3366ff\">DOI: 10.1021\/acs.jcim.5c02141<\/span><\/a><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.jcim.5c02141\/asset\/images\/medium\/ci5c02141_0008.gif\" alt=\"Abstract Image\" width=\"301\" height=\"181\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamamoto, Y.; Takenaka, S.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\nGold-Catalyzed Cyclization of Pyrrole-Tethered Allenynes for the Synthesis of 4-Acylindoles and Its Application to the Ergot Alkaloid Scaffold.\u00a0<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><em>Org. Lett<\/em>. <strong>2026<\/strong>, <em>28<\/em>, 1331\u20131336.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.5c05144\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.orglett.5c05144<\/a> <\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"color: #3366ff\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.orglett.5c05144\/asset\/images\/medium\/ol5c05144_0012.gif\" alt=\"Abstract Image\" width=\"398\" height=\"86\" \/>\r\n<\/span><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shimamoto, N.; Arichi, N.; Ohno, H.<\/span><\/div>\n<div class=\"capsule__title fixpadv--m\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif\">Triplet Nitrene-Mediated Photocatalytic Azidation of Tertiary C(sp<sup>3<\/sup>)\u2013H Bonds.<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><em>Chem. Commun.<\/em> <strong>2026<\/strong>,<span style=\"color: #000000\"><em> 62<\/em>, 164\u2013167.<\/span><\/span><\/div>\n<div><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2025\/CC\/D5CC05587C\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1039\/D5CC05587C<\/span><\/a><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2630\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128-300x150.png\" alt=\"\" width=\"300\" height=\"150\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128-300x150.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128-1024x511.png 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128-768x384.png 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128-1536x767.png 1536w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/12\/TOC251128.png 1894w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2025\"><\/a>2025<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Hasegawa, D.; Arichi, N.; Ohno, H.<\/span><\/div>\n<div class=\"article_header-title\"><span class=\"hlFld-Title\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Stereoselective Synthesis of Spirocyclic Indolin-3-ones through a Gold(I)-Catalyzed Cascade Cyclization of Azido-alkynes.<br \/>\n<em>J<\/em>. <em>Org<\/em>. <em>Chem<\/em>. <strong>2025<\/strong>, <em>90<\/em>, 11737\u201311741.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.5c01284\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.joc.5c01284<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.joc.5c01284\/asset\/images\/medium\/jo5c01284_0009.gif\" alt=\"Abstract Image\" width=\"300\" height=\"165\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shimamoto, N.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Photoinduced Azidosulfonylative Cyclizations of 1,6-Dienes with Sulfonyl Azides.<br \/>\n<em>Chem<\/em>. <em>Pharm<\/em>. <em>Bull<\/em>. <strong>2025<\/strong>, <em>73<\/em>, 831\u2013834.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1248\/cpb.c25-00437\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1248\/cpb.c25-00437<\/a><\/span><br \/>\n<\/span><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\" src=\"https:\/\/www.jstage.jst.go.jp\/pub\/cpb\/73\/9\/73_c25-00437\/figure\/73_c25-00437.png\" alt=\"\" width=\"410\" height=\"93\" \/><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Iwamoto, N.; Ohno, S.; Nakamura, K.; Naito, T.; Miura, S.; Inuki, S.; Ohno, H.; Hayashi, G.; Murakami, H.; Oishi, S.<br \/>\nDesign and Evaluation of Stable Cysteine-Modified Monobody Scaffolds for Mirror-Image Synthesis.<br \/>\n<em>Bioconjug. Chem.<\/em>\u00a0<strong>2025<\/strong>,\u00a0<em>36<\/em>, 1504\u20131515.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.5c00181\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.bioconjchem.5c00181<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.bioconjchem.5c00181\/asset\/images\/medium\/bc5c00181_0008.gif\" alt=\"Abstract Image\" width=\"360\" height=\"189\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Ohno, H.; Tsuji, A.; Hasegawa, D.; Inuki, S.; Arichi, N.<\/span><br \/>\n<span style=\"font-size: 12pt\">Synthetic Study of Caulerpin: Construction of the Core Structure through Gold-Catalyzed Cascade Cyclization of Azido-Alkynes.<b><br \/>\n<\/b><em>Chem<\/em>. <em>Pharm<\/em>. <em>Bull<\/em>. <strong>2025<\/strong>, <em>73<\/em>, 645\u2013649.<br \/>\n<span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1248\/cpb.c25-00268\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1248\/cpb.c25-00268<\/a><\/span><br \/>\n<\/span><\/span><\/span><\/p>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" src=\"https:\/\/www.jstage.jst.go.jp\/pub\/cpb\/73\/7\/73_c25-00268\/figure\/73_c25-00268.png\" alt=\"\" width=\"289\" height=\"160\" \/>\r\n<\/span><\/pre>\n<\/div>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Takahara, A.; Nakatsu, T.; Hirata, K.; Hayashi, H.; Kawaji, K.; Aoki, K.; Inuki, S.; Ohno, H.; Kato, H.; Kodama, E.; Oishi, S.<br \/>\nElucidation of Postfusion Structures of the Measles Virus F Protein for the Structure-Based Design of Fusion Inhibitors.<br \/>\n<em>J. Med. Chem.<\/em> <strong>2025<\/strong>,\u00a0<em>68<\/em>, 3123\u20133133.<br \/>\n<span style=\"color: #000080\"><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><a href=\"https:\/\/doi.org\/10.1021\/acs.jmedchem.4c02337\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.jmedchem.4c02337<\/span><\/a><\/span><br \/>\n<\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1399 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jm4c02337_0007\u306e\u30b3\u30d2\u309a\u30fc2.png\" alt=\"\" width=\"350\" height=\"91\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jm4c02337_0007\u306e\u30b3\u30d2\u309a\u30fc2.png 500w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jm4c02337_0007\u306e\u30b3\u30d2\u309a\u30fc2-300x78.png 300w\" sizes=\"auto, (max-width: 350px) 100vw, 350px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Akiba, H.; Ise, T.; Satoh, R.; Abe, Y.; Tsumoto, K.; Ohno, H.; Kamada, H.; Nagata, S.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Generation of antagonistic biparatopic anti-CD30 antibody from an agonistic antibody by precise epitope determination and utilization of structural characteristics of CD30 molecule<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>Antib. Ther.<\/em> <strong>2025<\/strong>, <em>8<\/em>, 56\u201367.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1093\/abt\/tbaf002\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1093\/abt\/tbaf002<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Suzuki, T.; Nojo, W.; Kawada, Y.; Sugiyama, S.; Ikeuchi, T.; Ishigaki, Y.; Ohno, H.<br \/>\nGold(I)-catalyzed Synthesis of Axially Chiral Indolo[2,3-<i>c<\/i>]carbazole Exhibiting Advanced Electrochromic Response.<br \/>\n<em>Asian J. Org. Chem.<\/em> <strong>2025<\/strong>, <em>14<\/em>, e202400695.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/ajoc.202400695\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/ajoc.202400695<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Watanabe, K.; Yamano, M.; Miyamoto, J.; Ohue-Kitano, R.; Masujima, Y.; Sasahara, D.; Mouri, Y.; Kono, N.; Inuki, S.; Osakada, F.; Nagaoka, K.; Aoki, J.; Sugiura, Y.; Ohno, H.; Kondoh, E.; Kimura, I.<br \/>\nMaternal progesterone and adipose mPR\u03b5 in pregnancy regulate the embryonic nutritional state.<br \/>\n<em>Cell Rep.<\/em> <strong>2025<\/strong>,\u00a0<em>44<\/em>, 115433.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.celrep.2025.115433\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.celrep.2025.115433<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Park, Y.; Matsumoto, S.; Ogata, K.; Ma, B.; Kanada, R.; Isaka, Y.; Arichi, N.; Liang, X.; Maki, R.; Kazasa, T.; Okuno, Y.; Ohno, H.; Ishihama, Y.; Toyoshima, F.<br \/>\nReceptor-independent regulation of G\u03b113 by alpha-1-antitrypsin C-terminal peptides.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>J. Biol. Chem.<\/em> <strong>2025<\/strong>, <em>301<\/em>, 108136.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.jbc.2024.108136\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.jbc.2024.108136<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shimizu, H.; Miyamoto, J.; Hisa, K.; Ohue-Kitano, R.; Takada, H.; Yamano, M.; Nishida, A.; Sasahara, D.; Masujima, Y.; Watanabe, K.; Nishikawa, S.; Takahashi, S.; Ikeda, T.; Nakajima, Y.; Yoshida, N.; Matsuzaki, C.; Kageyama, T.; Hayashi, I.; Matsuki, A.; Akashi, R.; Kitahama, S.; Ueyama, M.; Murakami, T.; Inuki, S.; Irie, J.; Satoh-Asahara, N.; Toju, H.; Mori, H.; Nakaoka, S.; Yamashita, T.; Toyoda, A.; Yamamoto, K.; Ohno, H.; Katayama, T.; Itoh, H.; Kimura, I.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sucrose-preferring Gut Microbes Prevent Host Obesity by Producing Exopolysaccharides.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>Nat. Commun.<\/em> <strong>2025<\/strong>, <em>16<\/em>, 1145.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1038\/s41467-025-56470-0\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1038\/s41467-025-56470-0<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Hasegawa, D.; Tsuji, A.; Greiner, L. C.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\n<\/span><\/div>\n<div><span class=\"hlFld-Title\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Synthesis of Azocine-Fused Indoles via Gold(I)-Catalyzed Cyclization of Azido-alkynes.<br \/>\n<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><em>J. Org. Chem.<\/em> <strong>2025<\/strong>, <em>90<\/em>, 925\u2013930.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.4c02704\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.joc.4c02704<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1395 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025JOC\u306e\u30b3\u30d2\u309a\u30fc.png\" alt=\"\" width=\"450\" height=\"92\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025JOC\u306e\u30b3\u30d2\u309a\u30fc.png 500w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025JOC\u306e\u30b3\u30d2\u309a\u30fc-300x61.png 300w\" sizes=\"auto, (max-width: 450px) 100vw, 450px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, T.; Takasaki, R.; Akiba, H.; Ogata, K.; Hattori, A.; Arichi, N.; Kakeya, H.; Yamasaki, S.; Ishihama, Y.; Ohno, H.; Inuki, S.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Visible light-mediated photocatalytic coupling between tetrazoles and carboxylic acids for biomolecule labelling.<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><em>Chem. Commun.<\/em> <strong>2025<\/strong>,<span style=\"color: #000000\"> <em>61<\/em>, 6320\u20136323.<br \/>\n<\/span><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1039\/D4CC04452E\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1039\/D4CC04452E<\/a> <\/span><\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1386 size-medium aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025CC-300x137.gif\" alt=\"\" width=\"300\" height=\"137\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025CC-300x137.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2025CC.gif 378w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2024\"><\/a>2024<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Takasaki, R.; Ito, E.; Nagae, M.; Takahashi, Y.; Matsuoka, T.; Yasue, W.; Arichi, N.; Ohno, H.; Yamasaki, S.; Inuki, S.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Development of Ribityllumazine Analog as Mucosal-associated Invariant T Cell Ligand.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>J. Am. Chem. Soc. <\/i><strong>2024<\/strong>, <em>146<\/em>, 29964\u201329976.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/jacs.4c12997\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/jacs.4c12997<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1285\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024_1-300x180.gif\" alt=\"\" width=\"230\" height=\"138\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024_1-300x180.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024_1.gif 500w\" sizes=\"auto, (max-width: 230px) 100vw, 230px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nakamura, S.; Nishiwaki, K.; Tsuyuguchi, M.; Kinoshita, T.; Oishi, S.; Ohni. H.; Nakanishi, I.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Compounds Designs of CK2\u03b1 Inhibitors Derived from Virtual Screening Hit Compounds by Computational Chemistry with Crystallography.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>Chem. Pharm. Bull.<\/em> <strong>2024<\/strong>, <em>72<\/em>, 776\u2013780.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt;color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1248\/cpb.c23-00824\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1248\/cpb.c23-00824<\/a><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1416 size-full aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/72_c23-00824.png\" alt=\"\" width=\"450\" height=\"194\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/72_c23-00824.png 450w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/72_c23-00824-300x129.png 300w\" sizes=\"auto, (max-width: 450px) 100vw, 450px\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Aoki, K.; Maeda, K.; Inuki, S.; Ohno, H.; Nonaka, M.; Oishi, S.<br \/>\nChemical Synthesis of Interleukin-6 for Mirror-Image Screening.<br \/>\n<em>Bioconjug. Chem.<\/em>\u00a0<strong>2024<\/strong>,\u00a0<em>35<\/em>, 1190\u20131199.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.bioconjchem.4c00204\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: doi\/10.1021\/acs.bioconjchem.4c00204<\/span><\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1415 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00204_0007\u306e\u30b3\u30d2\u309a\u30fc-300x160.png\" alt=\"\" width=\"270\" height=\"144\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00204_0007\u306e\u30b3\u30d2\u309a\u30fc-300x160.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00204_0007\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 270px) 100vw, 270px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Hashimoto, N.; Taguchi, J.; Kasagi, T.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\nConstruction of the Akuammiline Alkaloid Core Structure via Stereoselective E-ring Formation.<br \/>\n<i>J. Org. Chem. <\/i><strong>2024<\/strong>, <em>89<\/em>, 10388\u201310392.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt;color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.4c01105\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.joc.4c01105<\/a><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1315 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo4c01105_0009.gif\" alt=\"\" width=\"450\" height=\"104\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo4c01105_0009.gif 500w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo4c01105_0009-300x69.gif 300w\" sizes=\"auto, (max-width: 450px) 100vw, 450px\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Arichi, N.; Amano, T.; Wu, S.; Inuki, S.; Ohno, H.<br \/>\nSynthesis of Sulfilimines via Visible-Light-Mediated Triplet Energy Transfer to Sulfonyl Azides.<br \/>\n<i>Chem. Eur. J. <\/i><strong>2024<\/strong>, <em>30<\/em>, e202401842.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/chem.202401842\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/chem.202401842<\/a> <\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1290\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202401842-toc-0001-m-1024x248.jpg\" alt=\"\" width=\"400\" height=\"97\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202401842-toc-0001-m-1024x248.jpg 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202401842-toc-0001-m-300x73.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202401842-toc-0001-m-768x186.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202401842-toc-0001-m.jpg 1179w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Iwamoto, N.; Kai, T.; Inuki, S.; Ohno, H.; Maeda, H.; Watanabe, H.; Maruyama, T.; Oishi, S.<br \/>\nMirror-Image Human Serum Albumin Domain III as a Tool for Analyzing Site II-Dependent Molecular Recognition.<br \/>\n<em>Bioconjug. Chem<\/em>.\u00a0<strong>2024<\/strong>,\u00a0<em>35<\/em>, 816\u2013825. <span style=\"color: #000080\"><br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.4c00150\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.bioconjchem.4c00150<\/span><\/a><br \/>\n<\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"> <img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1421\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00150_0007\u306e\u30b3\u30d2\u309a\u30fc-300x141.png\" alt=\"\" width=\"350\" height=\"165\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00150_0007\u306e\u30b3\u30d2\u309a\u30fc-300x141.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc4c00150_0007\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 350px) 100vw, 350px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Aoki, K.; Higashi, K.; Oda, S.; Manabe, A.; Maeda, K.; Morise, J.; Oka, S.; Inuki, S.; Ohno, H.; Oishi, S.; Nonaka, M.<br \/>\nEngineering a Low-Immunogenic Mirror-Image VHH against Vascular Endothelial Growth Factor.<br \/>\n<em>ACS Chem. Biol<\/em>.\u00a0<strong>2024<\/strong>,\u00a0<em>19<\/em>, 1194\u20131205.<br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acschembio.4c00197\" class=\"liinternal\"><span style=\"color: #000080\"><span style=\"color: #3366ff\">DOI: 10.1021\/acschembio.4c00197<\/span><\/span><\/a><\/span><\/div>\n<p><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1420\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cb4c00197_0006\u306e\u30b3\u30d2\u309a\u30fc-300x128.png\" alt=\"\" width=\"300\" height=\"128\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cb4c00197_0006\u306e\u30b3\u30d2\u309a\u30fc-300x128.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cb4c00197_0006\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/> <\/span><\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yoshida, Y.; Takeuchi, H.; Arichi, N.; Oishi, S.; Ohno, H.; Inuki, S.<br \/>\nApproach to Spirocyclohexadienes via Visible Light-Mediated <em>ipso<\/em>-Cyclization of Amino Acid Derivatives with N-(2-Phenyl)benzoyl Groups.<br \/>\n<em>Asian J. Org. Chem. <\/em><strong>2024<\/strong>, <em>13<\/em>, e202400140.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/ajoc.202400140\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/ajoc.202400140<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Inuki, S.; Miyamoto, J.; Hashimoto, N.; Shimizu, H.; Tabuchi, H.; Kawai, A.; Greiner, L. C.; Kimura, I.; Ohno, H.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Structure-Activity Relationship Studies of Tetrahydroquinolone Derivatives as GPR41 Modulators.<br \/>\n<em>Bioorg. Med. Chem. Lett. <\/em><strong>2024<\/strong>,<em> 107<\/em>, 129758.<br \/>\n<span style=\"color: #000080\"><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.bmcl.2024.129758\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.bmcl.2024.129758<\/a><\/span><br \/>\n<\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1302\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMCL.jpg\" alt=\"\" width=\"450\" height=\"140\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMCL.jpg 500w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMCL-300x94.jpg 300w\" sizes=\"auto, (max-width: 450px) 100vw, 450px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Aoki, K.; Tsuda, S.; Ogata, N.; Kataoka, M.; Sasaki, J.; Inuki, S.; Ohno, H.; Watashi, K.; Yoshiya, T.; Oishi, S.<br \/>\nSynthetic Study of Full-length Hepatitis B Virus Core Protein and Its Capsid Formation.<br \/>\n<i>Org. Biomol. Chem. <\/i><strong>2024<\/strong>, <em>22<\/em>, 2218\u20132225.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1039\/D3OB02099A\" style=\"color: #3366ff\" class=\"liinternal\">DOI: doi.org\/10.1039\/D3OB02099A<\/a> <\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1306 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC-300x153.gif\" alt=\"\" width=\"300\" height=\"153\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC-300x153.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC.gif 370w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamaguchi, A.; Obiya, N.; Arichi, N.; Oishi, S.; Ohno, H.; Inuki, S.<br \/>\nSynthesis of Labionin and Avionin Precursors via Nitrogen-centred-radical-triggered 1,5-HAT Reaction of Tris Derivatives.<br \/>\n<i>Org. Biomol. Chem. <\/i><strong>2024<\/strong>, <em>22<\/em>, 2049\u20132055.<br \/>\n<span style=\"color: #000080\"><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1039\/D3OB02037A\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1039\/D3OB02037A<\/a><\/span><br \/>\n<\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1308\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC2.gif\" alt=\"\" width=\"400\" height=\"189\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC2.gif 378w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024OBC2-300x142.gif 300w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Iwamoto, N.; Sakaki, J.; Ohno, S.; Aoki, K.; Usui, Y.; Inuki, S.; Ohno, H.; Oishi, S.<br \/>\nSynthetic Studies on the Extracellular Domain of the T Cell Immunoreceptor with Immunoglobulin and Immunoreceptor Tyrosine-Based Inhibitory Motif Domain (TIGIT) Using Trt-K10 Solubilizing Tags.<br \/>\n<i>Bioorg. Med. Chem. <\/i><strong>2024<\/strong>, <em>99<\/em>, 117585.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.bmc.2023.117585\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.bmc.2023.117585<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1311 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-300x125.jpg\" alt=\"\" width=\"300\" height=\"125\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-300x125.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-1024x428.jpg 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-768x321.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-1536x641.jpg 1536w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2024BMC-2048x855.jpg 2048w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ito, E.; Inuki, S.; Izumi, Y.; Takahashi, M.; Dambayashi, Y.; Ciacchi, L.; Awad, W.; Takeyama, A.; Shibata, K.; Mori, S.; Mak, J. Y. W.; Fairlie, D. P.; Bamba, T.; Ishikawa, E.; Nagae, M.; Rossjohn, J.; Yamasaki, S.<br \/>\nSulfated Bile Acid is a Host-derived Ligand for MAIT Cells.<br \/>\n<i>Sci. Immunol. <\/i><strong>2024<\/strong>, <em>9<\/em>, eade6924.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/doi.org\/10.1126\/sciimmunol.ade6924\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1126\/sciimmunol.ade6924<\/span><\/a> <\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ohno, H.;\u00a0Arichi, N.; Inuki, S.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nonbiomimetic Total Synthesis of Polycyclic Alkaloids.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Modern Natural Product Synthesis: Overcoming Difficulties<\/i>, 1st ed; Springer, <strong>2024<\/strong>.<\/span><\/div>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2023\"><\/a>2023<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Akiba, H.; Fujita, J.; Ise, T.; Nishiyama, K.; Miyata, T.; Kato, T.; Namba, K.; Ohno, H.; Kamada, H.; Nagata, S.; Tsumoto, K.<br \/>\nDevelopment of a 1:1-Binding Biparatopic anti-TNFR2 Antagonist by Reducing Signaling Activity through Epitope Selection.<br \/>\n<i>Commun.<\/i> <em>Biol<\/em>. <strong>2023<\/strong>, <em>6<\/em>, 987.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1038\/s42003-023-05326-8\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1038\/s42003-023-05326-8<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Hashimoto, N.; Taguchi, J.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\nGold(I)-Catalyzed Cascade Cyclization of Alkynyl Indoles for the Stereoselective Construction of the Quaternary Carbon Center of Akuammiline Alkaloids.<br \/>\n<i>J. Org. Chem. <\/i><strong>2023<\/strong>, <em>88<\/em>, 17306\u201317321.<br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.3c02142\" class=\"liinternal\"><span style=\"color: #000080\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.joc.3c02142<\/span><\/span><\/a><br \/>\n<\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1429\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo3c02142_0013\u306e\u30b3\u30d2\u309a\u30fc-300x80.png\" alt=\"\" width=\"350\" height=\"94\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo3c02142_0013\u306e\u30b3\u30d2\u309a\u30fc-300x80.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo3c02142_0013\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 350px) 100vw, 350px\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Aoki, K.; Manabe, A.; Kimura, H.; Katoh, Y.; Inuki, S.; Ohno, H.; Nonaka, M.; Oishi, S.<br \/>\n<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Mirror-Image Single-Domain Antibody for a Novel Nonimmunogenic Drug Scaffold.<br \/>\n<i>Bioconjug.<\/i> <em>Chem<\/em>. <strong>2023<\/strong>, <em>34<\/em>, 2055\u20132065.<br \/>\n<span style=\"color: #3366ff\"><a href=\"http:\/\/doi.org\/10.1021\/ACS.BIOCONJCHEM.4C00150\" style=\"color: #3366ff\" class=\"liexternal\">DOI: <\/a><a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.3c00372\" class=\"underline mat-body-1 ng-star-inserted\" style=\"color: #3366ff\" target=\"_blank\" rel=\"noopener noreferrer\">10.1021\/acs.bioconjchem.3c00372<\/a> <\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1431\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc3c00372_0008\u306e\u30b3\u30d2\u309a\u30fc-300x206.png\" alt=\"\" width=\"270\" height=\"186\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc3c00372_0008\u306e\u30b3\u30d2\u309a\u30fc-300x206.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc3c00372_0008\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 270px) 100vw, 270px\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Iwamoto, N.; Sato, Y.; Manabe, A.; Inuki, S.; Ohno, H.; Nonaka, M.; Oishi, S.<br \/>\nDesign and Synthesis of Monobody Variants with Low Immunogenicity.<br \/>\n<i>ACS Med. Chem. Lett.<\/i> <strong>2023<\/strong>, <em>14<\/em>, 1596\u20131601.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.3c00342\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acsmedchemlett.3c00342<\/a><\/span><\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1432\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00342_0006\u306e\u30b3\u30d2\u309a\u30fc-300x155.png\" alt=\"\" width=\"300\" height=\"155\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00342_0006\u306e\u30b3\u30d2\u309a\u30fc-300x155.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00342_0006\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, T.; Hattori, A.; Oishi, S.; Araki, M.; Ma, B.; Fujii, T.; Arichi, N.; Okuno, Y.; Kakeya, H.; Yamasaki, S.; Ohno, H.; Inuki, S.<br \/>\nEstablishment of an MR1-Presentation Reporter Screening System and Identification of Phenylpropanoid Derivatives as MR1 Ligands.<br \/>\n<i>J. Med. Chem. <\/i><strong>2023<\/strong>, <em>66<\/em>, 12520\u201312535.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.jmedchem.3c01122\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.jmedchem.3c01122 <\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1393\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JMC-300x161.jpg\" alt=\"\" width=\"360\" height=\"193\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JMC-300x161.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JMC-768x412.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JMC.jpg 990w\" sizes=\"auto, (max-width: 360px) 100vw, 360px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Oka, S.; Watanabe, M.; Ito, E.; Takeyama, A.; Matsuoka, T.; Takahashi, M.; Izumi, Y.; Arichi, N.; Ohno, H.; Yamasaki, S.; Inuki, S.<br \/>\nArchaeal Glycerolipids Are Recognized by C-type Lectin Receptor Mincle.<br \/>\n<i>J. Am. Chem. Soc.<\/i>\u00a0<strong>2023<\/strong>, <em>145<\/em>, 18538\u201318548.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/jacs.3c05473\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/jacs.3c05473<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1390 aligncenter\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JACS-300x158.jpg\" alt=\"\" width=\"350\" height=\"184\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JACS-300x158.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JACS-768x404.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/2023JACS.jpg 902w\" sizes=\"auto, (max-width: 350px) 100vw, 350px\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Suzuki, R.; Mattos, D. R.; Kitamura, T.; Tsujioka, R.; Kobayashi, K.; Inuki, S.; Ohno, H.; Ishmael, J. E.; McPhail, K. L.; Oishi, S.<br \/>\nDesign of Synthetic Surrogates for the Macrolactone Linker Motif in Coibamide A.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>ACS Med. Chem. Lett.<\/i> <strong>2023<\/strong>, <em>14<\/em>, 1344\u20131350.<br \/>\n<\/span><\/div>\n<div><span style=\"color: #3366ff;font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.3c00232\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acsmedchemlett.3c00232<\/a> <\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1434\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00232_0004\u306e\u30b3\u30d2\u309a\u30fc-300x163.png\" alt=\"\" width=\"300\" height=\"163\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00232_0004\u306e\u30b3\u30d2\u309a\u30fc-300x163.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml3c00232_0004\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tsuno, H.; Shen, J.; Komatsu, H.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Gold(I)\u2010Catalyzed Bis\u2010Cyclization of Allenynes for the Synthesis of Strained and Planar Polycyclic Compounds.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Angew. Chem. Int. Ed.<\/i> <strong>2023<\/strong>, <em>62<\/em>, e202307532.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.202307532\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.202307532<\/a><\/span><br \/>\n<\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1436 alignnone\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202307532-toc-0001-m-300x99.jpg\" alt=\"\" width=\"400\" height=\"131\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202307532-toc-0001-m-300x99.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202307532-toc-0001-m.jpg 648w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Yoshida, Y.; Takeuchi, H.; Nakagawa, K.; Fujii, T.; Arichi, N.; Oishi, S.; Ohno, H.; Inuki, S.<br \/>\nConstruction of a Bicyclo[2.2.2]octene Skeleton via a Visible-Light-Mediated Radical Cascade Reaction of Amino Acid Derivatives with N-(2-Phenyl)benzoyl Groups.<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><i>Org. Lett.<\/i>\u00a0<strong>2023<\/strong>, <em>25<\/em>, 4846\u20134851.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.3c01586\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.orglett.3c01586<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1437\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ol3c01586_0008\u306e\u30b3\u30d2\u309a\u30fc-300x104.png\" alt=\"\" width=\"300\" height=\"104\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ol3c01586_0008\u306e\u30b3\u30d2\u309a\u30fc-300x104.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ol3c01586_0008\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Nishiyama, K.; Akiba, H.; Nagata, S.; Tsumoto, K.; Kamada, H.; Ohno, H.<br \/>\nA Proximity-Induced Fluorogenic Reaction Triggered by Antibody\u2013Antigen Interactions with Adjacent Epitopes.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Angew. Chem. Int. Ed.<\/i> <strong>2023<\/strong>, <em>62<\/em>, e202306431.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.202306431\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.202306431<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1438\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202306431-toc-0001-m-300x219.jpg\" alt=\"\" width=\"300\" height=\"219\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202306431-toc-0001-m-300x219.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202306431-toc-0001-m.jpg 648w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/>\r\n<\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Greiner, L. C.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\nAlkoxymigration onto \u03b1-Imino Gold Carbenes for Constructing Propellane-Type Indolines.<br \/>\n<i>Asian J. Org.<\/i> <em>Chem<\/em>. <strong>2023<\/strong>, <em>12<\/em>, e202300232.<br \/>\n<a href=\"https:\/\/doi.org\/10.1002\/ajoc.202300232\" class=\"liinternal\"><span style=\"color: #000080\"><span style=\"color: #3366ff\">DOI: 10.1002\/ajoc.202300232<\/span><\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tsuji, A.; Masuya, T.; Arichi, N.; Inuki, S.; Murai, M.; Miyoshi, H.; Ohno, H.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Discovery of Bis-sulfonamides as Novel Inhibitors of Mitochondrial NADH-Quinone Oxidoreductase (Complex I).<br \/>\n<\/span><\/div>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><i>ACS Med. Chem. Lett.<\/i> <strong>2023<\/strong>, <em>14<\/em>, 211\u2013216.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.2c00504\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acsmedchemlett.2c00504<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1441\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml2c00504_0010\u306e\u30b3\u30d2\u309a\u30fc-1-300x95.png\" alt=\"\" width=\"400\" height=\"126\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml2c00504_0010\u306e\u30b3\u30d2\u309a\u30fc-1-300x95.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml2c00504_0010\u306e\u30b3\u30d2\u309a\u30fc-1.png 500w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Greiner, L. C.; Arichi, N.; Inuki, S.; Ohno, H.<br \/>\nGold(I)-Catalyzed Benzylic C(sp3)-H Functionalizations: Divergent Synthesis of Indole[a]- and [b]-Fused Polycycles.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Angew. Chem. Int. Ed.<\/i> <strong>2023<\/strong>, <em>62<\/em>, e202213653.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.202213653\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.202213653<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><span style=\"color: #000080\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1443\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202213653-toc-0001-m-300x65.jpg\" alt=\"\" width=\"500\" height=\"109\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202213653-toc-0001-m-300x65.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202213653-toc-0001-m-1024x222.jpg 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202213653-toc-0001-m-768x167.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202213653-toc-0001-m.jpg 1299w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/>\r\n<\/span><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miyamoto, J; Shimizu, H.; Hisa, K.; Matsuzaki, C.; Inuki, S.; Ando, Y.; Nishida, A.; Izumi, A.; Yamano, M.; Ushiroda, C.; Irie, J.; Katayama, T.; Ohno, H.; Itoh, H.; Yamamoto, K.; Kimura, I.<br \/>\nHost metabolic benefits of prebiotic exopolysaccharides produced by <em>Leuconostoc mesenteroides<\/em>.<br \/>\n<i>Gut Microbes\u00a0<\/i><strong>2023<\/strong>, <em>15<\/em>, 2161271.<br \/>\n<a href=\"https:\/\/doi.org\/10.1080\/19490976.2022.2161271\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: <\/span><span style=\"color: #000080\"><span style=\"color: #3366ff\">10.1080\/19490976.2022.2161271<\/span><\/span><\/a><\/span><\/div>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2022\"><\/a>2022<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yagi, M.; Miller, S.; Nagai, Y.; Inuki, S.; Sato, A.; Hirora, T.<br \/>\nA methylbenzimidazole derivative regulates mammalian circadian rhythms by targeting Cryptochrome proteins.<br \/>\n<em>F1000Research<\/em>\u00a0<strong>2022<\/strong>, <em>11<\/em>, 1016.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.12688\/f1000research.124658.2\" style=\"color: #3366ff\" class=\"liinternal\">DOI:\u00a0<span class=\"identifier doi\">10.12688\/f1000research.124658.2<\/span><\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamamoto, A.; Takahashi, Y.; Inuki, S.; Nakagawa, S.; Nakao, K.; Ohno, H.; Doi, M.; Takakura, Y.<br \/>\nThe identification of novel small extracellular vesicle (sEV) production modulators using luciferase-based sEV quantification method.<br \/>\n<em>J. Extracell. Biol<\/em>.<em>\u00a0<\/em><strong>2022<\/strong>, <em>1<\/em>, e62.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/jex2.62\" style=\"color: #3366ff\" class=\"liinternal\">DOI:<span class=\"identifier doi\"> 10.1002\/jex2.62<\/span><\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Inuki, S.; Tabuchi, H.; Matsuzaki, C.; Yonejima, Y.; Hisa, K.; Kimura, I.; Yamamoto, K.; Ohno, H.<br \/>\nChemical Synthesis and Evaluation of Exopolysaccharide Fragments Produced by Leuconostoc mesenteroides strain NTM048.<br \/>\n<em>Chem. Pharm. Bull.<\/em>\u00a0<strong>2022<\/strong>, <em>70<\/em>, 155\u2013161.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1248\/cpb.c21-00919\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1248\/cpb.c21-00919<\/a> <\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kitamura, T.; Suzuki, R.; Inuki, S.; Ohno, H.; McPhail, K. L.; Oishi, S.<br \/>\nDesign of coibamide A mimetics with improved cellular bioactivity.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>ACS Med. Chem. Lett.\u00a0<\/em><strong>2022<\/strong>, <em>13<\/em>, 105\u2013110.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.1c00591\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acsmedchemlett.1c00591<\/span><\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1460\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml1c00591_0007\u306e\u30b3\u30d2\u309a\u30fc-300x182.png\" alt=\"\" width=\"300\" height=\"182\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml1c00591_0007\u306e\u30b3\u30d2\u309a\u30fc-300x182.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/ml1c00591_0007\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2021\"><\/a>2021<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Komatsu, H.; Ikeuchi, T.; Tsuno, H.; Arichi, N.; Yasui, K.; Oishi, S.; Inuki, S.; Fukazawa, A.; Ohno, H.<br \/>\nConstruction of Tricyclic Nitrogen Heterocycles by Gold(I)-Catalyzed Cascade Cyclization of Allenynes and Its Application to Polycyclic \u03c0-Electron Systems.<br \/>\n<em>Angew. Chem. Int. Ed.\u00a0<\/em><strong>2021<\/strong>, <em>60<\/em>, 27019\u201327025.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt;color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.202111267\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.202111267<\/a><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1465\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-300x65.jpg\" alt=\"\" width=\"500\" height=\"108\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-300x65.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-1024x222.jpg 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-768x166.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-1536x333.jpg 1536w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202111267-toc-0001-m-2048x444.jpg 2048w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/> <i><i> <\/i><\/i><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Greiner, L. C.; Inuki, S.; Arichi, N.; Oishi, S.; Suzuki, R.; Iwai, T.; Sawamura, M.; Hashmi, A. S. K.; Ohno, H.<br \/>\nAccess to Indole-Fused Benzannulated Medium-Sized Rings through Gold(I)-Catalyzed Cascade Cyclization of Azido-Alkynes.<br \/>\n<em>Chem. Eur. J.<\/em> <strong>2021<\/strong>, <em>27<\/em>, 12992\u201312997.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/chem.202101824\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/chem.202101824<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1584 size-medium\" style=\"color: #000080\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202101824-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc-300x92.png\" alt=\"\" width=\"300\" height=\"92\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202101824-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc-300x92.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202101824-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, T.; Motozono, C.; Hattori, A.; Hideaki, K.; Yamasaki, S.; Oishi, S.; Ohno H.; Inuki, S.<br \/>\nThe Effects of 5\u2010OP\u2010RU Stereochemistry on Its Stability and MAIT\u2010MR1 Axis.<br \/>\n<em>ChemBioChem.\u00a0<\/em><strong>2021<\/strong>, <em>22<\/em>, 672\u2013678.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/cbic.202000466\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/cbic.202000466<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1583 size-medium\" style=\"color: #000080\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cbic202000466-toc-0001-m-300x213.jpg\" alt=\"\" width=\"300\" height=\"213\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cbic202000466-toc-0001-m-300x213.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/cbic202000466-toc-0001-m.jpg 426w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamaguchi, A.; Inuki, S.; Ohta, K.; Oishi, S.; Asai, A.; Ohno, H.<br \/>\nIdentification of a Novel Indoleamine 2,3-Dioxygenase Inhibitor Bearing an Eight-Membered Ring Fused Indole Scaffold and Its Structure-Activity Relationship.<br \/>\n<em>Heterocycles<\/em> <strong>2021<\/strong>, <em>103<\/em>, 331\u2013347.<br \/>\n<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">L. C. Greiner, J. Matsuoka, S. Inuki, H. Ohno<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Azido-Alkynes in Gold(I)-Catalyzed Indole Syntheses.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Chem. Rec.<\/i> <strong>2021<\/strong>, <em>21<\/em>, 3897\u20133910.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/tcr.202100202\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/tcr.202100202<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ohno, H.; Inuki, S.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nonbiomimetic total synthesis of indole alkaloids using alkyne-based strategies.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Org. Biomol.<\/i> <em>Chem<\/em>. <strong>2021<\/strong>, <em>19<\/em>, 3551\u20133568.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1039\/D0OB02577A\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1039\/D0OB02577A<\/a><\/span><\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2227\" style=\"font-family: Consolas, Monaco, monospace\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/Get-300x152.gif\" alt=\"\" width=\"300\" height=\"152\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/Get-300x152.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/Get.gif 372w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Inuki, S.; Ohno, H.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Total Syntheses of Myriocin, Mycestericins and Sphingofungin E: Sphingosine Analogues Containing a \u03b2, \u03b2'-Dihydroxy\u03b1-Amino Acid Framework.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>Chem. Lett.<\/i> <strong>2021<\/strong>, <em>50<\/em>, 1313\u20131324.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1246\/cl.210133\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1246\/cl.210133<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Arichi, N.; Ohno, H.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Natural Product Synthesis via Palladium-Catalyzed C\u2013H Bond Activation.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><i>In Handbook of CH-Functionalization, Ed. by D. Maiti, Wiley-VCH,<\/i> Weinheim, <strong>2021<\/strong><i>.<\/i><\/span><\/div>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2020\"><\/a>2020<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Takeuchi, H.; Inuki, S.; Nakagawa, K.; Kawabe, T.; Ichimura, A.; Oishi, S.; Ohno H.<br \/>\nTotal Synthesis of Zephycarinatines via Photocatalytic Reductive Radical ipso-Cyclization.<br \/>\n<em>Angew. Chem. Int. Ed.\u00a0<\/em><strong>2020<\/strong>, <em>59<\/em>, 21210\u201321215.<br \/>\n<a href=\"https:\/\/doi.org\/10.1002\/anie.202009399\" class=\"liinternal\"><span style=\"color: #000080\"><span style=\"color: #3366ff\">DOI: 10.1002\/anie.202009399<\/span><\/span><\/a><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1586\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202009399-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc-300x81.png\" alt=\"\" width=\"300\" height=\"81\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202009399-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc-300x81.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie202009399-toc-0001-m\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, J.; Inuki, S.; Matsuda, Y.; Miyamoto, Y.; Otani, M.; Oka, M.; Oishi, S.; Ohno, H.<br \/>\nTotal Synthesis of Dictyodendrins A\u2013F by the Gold-Catalyzed Cascade Cyclization of Conjugated Diyne with Pyrrole.<br \/>\n<em>Chem. Eur. J.<\/em>\u00a0<strong>2020<\/strong>, <em>26<\/em>, 11150\u201311157.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202001950\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1002\/chem.202001950<\/span><\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2010\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202001950-toc-0001-m-283x300.jpg\" alt=\"\" width=\"300\" height=\"318\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202001950-toc-0001-m-283x300.jpg 283w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/chem202001950-toc-0001-m.jpg 372w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, T.; Inuki, S.; Miyagawa, T.; Oishi, S.; Ohno, H.<br \/>\nTotal Synthesis of (+)-Polyoxamic Acid via Visible-Light-Mediated Photocatalytic \u03b2-Scission and 1,5-Hydrogen Atom Transfer of Glucose Derivative.<br \/>\n<em>J. Org. Chem<\/em>. <strong>2020<\/strong>, <em>85<\/em>, 8271\u20138278.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.0c00910\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.joc.0c00910<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2015\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo0c00910_0010\u306e\u30b3\u30d2\u309a\u30fc-300x87.png\" alt=\"\" width=\"300\" height=\"87\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo0c00910_0010\u306e\u30b3\u30d2\u309a\u30fc-300x87.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo0c00910_0010\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kimura, I.; Miyamoto, J.; Ohue-Kitano, R.; Watanabe, K.; Yamada, T.; Onuki, M.; Aoki, R.; Isobe, Y.; Kashihara, D.; Inoue, D.; Inaba, A.; Takamura, Y.; Taira, S.; Kumaki, S.; Watanabe, M.; Ito, M.; Nakagawa, F.; Irie, J.; Kakuta, H.; Shinohara, M.; Iwatsuki, K.; Tsujimoto, G.; Ohno, H.; Arita, M.; Itoh, H.; Hase, K.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Maternal gut microbiota in pregnancy influences offspring metabolic phenotype in mice.<br \/>\n<em>Science<\/em> <strong>2020<\/strong>,\u00a0<em>367<\/em>, eaaw8429.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1126\/science.aaw8429\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1126\/science.aaw8429<\/a><\/span><br \/>\n<\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">\r\n<img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2014\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/367_aaw8429_fa-300x191.jpeg\" alt=\"\" width=\"270\" height=\"172\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/367_aaw8429_fa-300x191.jpeg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/367_aaw8429_fa-1024x654.jpeg 1024w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/367_aaw8429_fa-768x490.jpeg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/367_aaw8429_fa.jpeg 1280w\" sizes=\"auto, (max-width: 270px) 100vw, 270px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sasaki, T.; Sonoda, T.; Tatebayashi, R.; Kitagawa, Y.; Oishi, S.; Yamamoto, K.; Fujii, N.; Inoue, N.; Uenoyama, Y.; Tsukamura, H.; Maeda, K.; Matsuda, F.; Morita, Y.; Matsuyama, S.; Ohkura, S.<br \/>\nPeripheral administration of SB223412, a selective neurokinin-3 receptor antagonist, suppresses pulsatile luteinizing hormone secretion by acting on the gonadotropin-releasing hormone pulse generator in estrogen-treated ovariectomized female goats.<br \/>\n<em>J. Reprod. Dev. <\/em><strong>2020<\/strong>,\u00a0<em>59<\/em>, 21210\u20132121.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1262\/jrd.2019-145\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1262\/jrd.2019-145<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miller, S.; Son, Y. L.; Aikawa, Y.; Makino, E.; Nagai, Y.; Srivastava, A.; Oshima, T.; Sugiyama, A.; Hara, A.; Abe, K.; Hirata, K.; Oishi, S.; Hagihara, S.; Sato, A.; Tama, F.; Itami, K.; Kay, S. A.; Hatori, M.; Hirota, T.<br \/>\nIsoform-selective regulation of mammalian cryptochromes.<br \/>\n<em>Nat. Chem. Biol.<\/em> <strong>2020<\/strong>,\u00a0<em>16<\/em>, 676\u2013685.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/doi.org\/10.1038\/s41589-020-0505-1\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1038\/s41589-020-0505-1<\/span><\/a><\/span><br \/>\n<\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2013\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/41589_2020_505_Figa_-300x133.png\" alt=\"\" width=\"300\" height=\"133\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/41589_2020_505_Figa_-300x133.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/41589_2020_505_Figa_.png 685w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamaguchi, A.; Inuki, S.; Tokimizu, Y.; Oishi, S.; Ohno, H.<br \/>\nGold(I)-Catalyzed Cascade Cyclization of Anilines with Diynes: Controllable Formation of Eight-Membered Ring-Fused Indoles and Propellane-Type Indolines.<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em>, 2543\u20132559.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.9b03256\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.joc.9b03256<\/span><\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2016\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo9b03256_0013-300x83.gif\" alt=\"\" width=\"300\" height=\"83\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo9b03256_0013-300x83.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_jo9b03256_0013.gif 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/span><\/pre>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2019\"><\/a>2019<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Tokunaga, M.; Miyamoto, Y.; Suzuki, T.; Otani, M.; Inuki, S.; Esaki, T.; Nagao, C.; Mizuguchi, K.; Ohno, H.; Yoneda, Y.; Okamoto, T.; Oka, M.; Matsuura, Y.<br \/>\nNovel anti-flavivirus drugs targeting the nucleolar distribution of core protein.<br \/>\n<em>Viology<\/em> <strong>2019<\/strong>, <em>541<\/em>, 41\u201351.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.virol.2019.11.015\" style=\"color: #3366ff\" class=\"liinternal\">DOI:<\/a><a href=\"https:\/\/doi.org\/10.1016\/j.virol.2019.11.015\" style=\"color: #3366ff\" class=\"liinternal\"><span class=\"identifier doi\"> 10.1016\/j.virol.2019.11.015<\/span><\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Rahayu, L.; Endo, N.; Kuwai, S.; Oishi, S.; Tanaka, T.<br \/>\nThe efficacy of a newly developed neurokinin 3 receptor agonist B21-750 on luteinizing hormone secretion in cycling goats.<br \/>\n<em>J. Reprod. Dev.<\/em> <strong>2019<\/strong>, <em>65<\/em>, 481\u2013484.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1262\/jrd.2019-038\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1262\/jrd.2019-038<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miyagawa, T.; Inuki, S.; Oishi, S.; Ohno, H.<br \/>\nConstruction of Quaternary Carbon Stereocenter of \u03b1-Tertiary Amine through Remote C\u2013H Functionalization of Tris Derivatives: Enantioselective Total Synthesis of Myriocin.<br \/>\n<em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em>, 5458\u20135490.<br \/>\n<span style=\"color: #000080\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.9b01778\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.orglett.9b01778<\/span><\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2018\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2019-017785_0009-300x103.gif\" alt=\"\" width=\"360\" height=\"124\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2019-017785_0009-300x103.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2019-017785_0009.gif 500w\" sizes=\"auto, (max-width: 360px) 100vw, 360px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, J.; Kumagai, H.; Inuki, S.; Oishi, S.; Ohno, H.<br \/>\nConstruction of the pyrrolo[2,3-d]carbazole core of spiroindoline alkaloids by gold-catalyzed cascade cyclization of ynamide.<br \/>\n<em>J. Org. Chem.<\/em> <strong>2019<\/strong>,\u00a0<em>84<\/em>, 9358\u20139363.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.9b01149\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.joc.9b01149<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><span style=\"color: #000080\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2020\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo-2019-011499_0009\u306e\u30b3\u30d2\u309a\u30fc-300x53.png\" alt=\"\" width=\"400\" height=\"71\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo-2019-011499_0009\u306e\u30b3\u30d2\u309a\u30fc-300x53.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/jo-2019-011499_0009\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/>\r\n<\/span><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Ikeuchi, T.; Inuki, S.; Oishi, S.; Ohno, H.<\/span><br \/>\n<span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Gold(I)-catalyzed cascade cyclization reactions of allenynes for the synthesis of fused cyclopropanes and acenaphthenes.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em>, 7792\u20137796.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.201903384\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.201903384<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><span style=\"color: #000080\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2026\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie201903384-toc-0001-m-300x200.jpg\" alt=\"\" width=\"300\" height=\"200\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie201903384-toc-0001-m-300x200.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/anie201903384-toc-0001-m.jpg 432w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamamoto, K.; Inuki, S.; Ohno, H.; Oishi, S.<br \/>\nScaffold hopping of fused piperidine-type NK3 receptor antagonists to reduce environmental impact.<br \/>\n<em>Bioorg. Med. Chem.<\/em> <strong>2019<\/strong>, <em>27<\/em>, 2019\u20132026.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.bmc.2019.03.059\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.bmc.2019.03.059<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2024\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/1-s2.0-S0968089619304353-ga1-300x104.jpg\" alt=\"\" width=\"360\" height=\"125\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/1-s2.0-S0968089619304353-ga1-300x104.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/1-s2.0-S0968089619304353-ga1.jpg 500w\" sizes=\"auto, (max-width: 360px) 100vw, 360px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Shu, K.; Iwamoto, N.; Honda, K.; Kondoh, Y.; Hirano, H.; Osada, H.; Ohno, H.; Fujii, N.; Oishi, S.<br \/>\nDevelopment of mirror-image screening systems for XIAP BIR3 domain inhibitors.<br \/>\n<em>Bioconjug. Chem.<\/em> <strong>2019<\/strong>, 30, 1395\u20131404.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.9b00154\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.bioconjchem.9b00154<\/a><\/span><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2023\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc-2019-00154t_0012\u306e\u30b3\u30d2\u309a\u30fc-300x137.png\" alt=\"\" width=\"300\" height=\"137\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc-2019-00154t_0012\u306e\u30b3\u30d2\u309a\u30fc-300x137.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/bc-2019-00154t_0012\u306e\u30b3\u30d2\u309a\u30fc.png 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\">Sasaki, T.; Ito, D.; Sonoda, T.; Morita, Y.; Wakabayashi, Y.; Yamamura, T.; Okamura, H.; Oishi, S.; Noguchi, T.; Fujii, N.; Uenoyama, Y.; Tsukamura, H.; Maeda, K.-I.; Matsuda, F.; Ohkura, S.<br \/>\nPeripheral administration of \u03ba-opioid receptor antagonist stimulates gonadotropin-releasing hormone pulse generator activity in ovariectomized, estrogen-treated female goats.<br \/>\n<em>Domest. Anim. Endocrinol.<\/em> <strong>2019<\/strong>, <em>68<\/em>, 83\u201391.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.domaniend.2018.12.011\" style=\"color: #3366ff\" class=\"liinternal\">DOI:\u00a010.1016\/j.domaniend.2018.12.011<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamamoto, K.; Yoshikawa, Y.; Ohue, M.; Inuki, S.; Ohno, H.; Oishi, S.<br \/>\n<\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Synthesis of triazolo- and oxadiazolo-piperazines by gold(I)-catalyzed domino cyclization: application to the design of a MAP kinase inhibitor.<br \/>\n<em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em>, 373\u2013377.<span style=\"color: #000080\"><br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b03500\" style=\"color: #000080\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.orglett.8b03500<\/span><\/a><br \/>\n<\/span><\/span><\/div>\n<pre><span style=\"font-size: 12pt;font-family: tahoma, arial, helvetica, sans-serif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2022\" style=\"color: #000080\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2018-03500j_0010-300x101.gif\" alt=\"\" width=\"300\" height=\"101\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2018-03500j_0010-300x101.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/images_medium_ol-2018-03500j_0010.gif 500w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/span><\/pre>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2018\"><\/a>2018<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kawada, Y.; Ohmura, S.; Kobayashi, M.; Nojo, W.; Kondo, M.; Matsuda, Y.; Matsuoka, J.; Inuki, S.; Oishi, S.; Wang, C.; Saito, T.; Uchiyama, M.; Suzuki, T.; Ohno, H.<br \/>\nDirect synthesis of aryl-annulated [c]carbazoles by gold(I)-catalysed cascade reaction of azide-diynes and arenes.<br \/>\n<em>Chem. Sci.<\/em> <strong>2018<\/strong>, <em>44<\/em>, 8416\u20138425.<br \/>\n<a href=\"https:\/\/doi.org\/10.1039\/C8SC03525C\" class=\"liinternal\"><span style=\"color: #000080\"><span style=\"color: #3366ff\">DOI: <\/span><span style=\"color: #3366ff\">10.1039\/C8SC03525C<\/span><\/span><\/a><\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2028\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/Get-300x152.gif\" alt=\"\" width=\"300\" height=\"152\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/Get-300x152.gif 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/06\/Get.gif 373w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Hamada, N.; Yamaguchi, A.; Inuki, S.; Oishi, S.; Ohno, H.<br \/>\nGold(I)-Catalyzed Oxidative Cascade Cyclization of 1,4-Diyn-3-ones for the Construction of Tropone-Fused Furan Scaffolds.<br \/>\n<em>Org. Lett.<\/em>\u00a0<strong>2018<\/strong>, <em>20<\/em>, 4401\u20134405.<\/span><\/div>\n<div><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b01524\" style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt;color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.orglett.8b01524<\/a><\/span><\/div>\n<pre><img decoding=\"async\" style=\"font-family: Consolas, Monaco, monospace\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.orglett.8b01524\/asset\/images\/medium\/ol-2018-01524f_0011.gif\" alt=\"Abstract Image\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Inuki, S.; Miyagawa, T.; Oishi, S.; Ohno, H.<br \/>\nIntroduction of a Polar Functional Group to the Lipid Tail of 4-<em>epi<\/em>-Jaspine B Affects Sphingosine Kinase Isoform Selectivity.<br \/>\n<em>Chem. Pharm. Bull.<\/em> <strong>2018<\/strong>, <em>66<\/em>, 866\u2013872.<\/span><\/div>\n<div><span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1248\/cpb.c18-00366\" style=\"color: #3366ff\" class=\"liinternal\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif\">DOI: 10.1248\/cpb.c18-00366<\/span><\/a><br \/>\n<\/span><\/div>\n<pre><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-2280\" style=\"color: #3366ff;font-family: Consolas, Monaco, monospace\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/66_c18-00366-300x149.png\" alt=\"\" width=\"300\" height=\"149\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/66_c18-00366-300x149.png 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/files\/2025\/07\/66_c18-00366.png 473w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kaneda, M.; Kawaguchi, S.; Fujii, N.; Ohno, H.; Oishi, S.<br \/>\n<\/span><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Structure\u2013Activity Relationship Study on Odoamide: Insights into the Bioactivities of Aurilide-Family Hybrid Peptide-Polyketides.<br \/>\n<\/span><em style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">ACS Med. Chem. Lett.<\/em> <strong style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">2018<\/strong><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">, <\/span><em style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">9<\/em><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">, 365\u2013369.<\/span><span style=\"color: #3366ff\"><br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.8b00028\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acsmedchemlett.8b00028<\/a><\/span><\/div>\n<pre><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><span style=\"color: #3366ff\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acsmedchemlett.8b00028\/asset\/images\/medium\/ml-2018-000288_0007.gif\" alt=\"Abstract Image\" width=\"500\" height=\"240\" \/><\/span><\/span><\/pre>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ohara, T.; Kaneda, M.; Saito, T.; Fujii, N.; Ohno, H. Oishi, S.<br \/>\nHead-to-tail macrocyclization of cysteine-free peptides using an o-aminoanilide linker.<br \/>\n<em>Bioorg. Med. Chem. Lett.<\/em> <strong>2018<\/strong>, <em>28<\/em>, 1283\u20131286.\u00a0<\/span><br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.bmcl.2018.03.027\" style=\"color: #3366ff\" class=\"liinternal\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif\">DOI: 10.1016\/j.bmcl.2018.03.027<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sekiguchi, H.; Kuroyanagi,T.; Rhainds, D.; Kobayashi, K.; Kobayashi, Y.; Ohno, H.; Heveker, N.; Akaji, K.; Fujii, N.; Oishi, S.<br \/>\nStructure\u2013activity relationship study of cyclic pentapeptide ligands for atypical chemokine receptor 3 (ACKR3).<br \/>\n<em>J. Med. Chem.<\/em> <strong>2018<\/strong>, <em>61<\/em>, 3745\u20133751.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jmedchem.8b00336\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.jmedchem.8b00336<\/a><\/span><br \/>\n<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kobayashi, Y.; Hoshino, M.; Kameda, T.; Kobayashi, K.; Akaji, K.; Inuki, S.; Ohno, H.; Oishi, S.<br \/>\nUse of a Compact Tripodaltris(bipyridine) Ligand to Stabilize a Single-Metal-Centered Chirality: Stereoselective Coordination of Iron(II) and Ruthenium(II) on a Semirigid Hexapeptide Macrocycle.<br \/>\n<em>Inorg. Chem.<\/em> <strong>2018<\/strong>, <em>57<\/em>, 5475\u20135485.<\/span><br \/>\n<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.inorgchem.8b00416\" class=\"liinternal\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif;color: #3366ff\">DOI: 10.1021\/acs.inorgchem.8b00416<\/span><\/a><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miyazaki, Y.; Ichimura, A.; Sato, S.; Fujii, T.; Oishi, S.; Sakai, H.; Takeshima, H.<br \/>\nThe natural flavonoid myricetin inhibits gastric H+, K+-ATPase.<br \/>\n<em>Eur. J. Pharmacol.<\/em> <strong>2018<\/strong>, <em>820<\/em>, 217\u2013221.<br \/>\n<a href=\"https:\/\/doi.org\/10.1016\/j.ejphar.2017.12.042\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1016\/j.ejphar.2017.12.042<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tsuda, S.; Mochizuki, M.; Ishiba, H.; Yoshizawa-Kumagaye, K.; Nishio, H.; Oishi, S.; Yoshiya, T.<br \/>\nEasy-to-Attach\/Detach Solubilizing-Tag-Aided Chemical Synthesis of an Aggregative Capsid Protein.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em> <strong>2018<\/strong>, <em>57<\/em>, 2105\u20132109.<br \/>\n<a href=\"https:\/\/doi.org\/10.1002\/anie.201711546\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1002\/anie.201711546<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miyagawa, T.; Inuki, S.; Honda, M.; Nakamura, S.; Nakanishi, I.; Fujii, N.; Oishi, S.; Ohno, H.<br \/>\nSynthesis of jaspine B regioisomers through palladium-catalyzed stereoselective tetrahydrofuran formation: insight into the ligand recognition of sphingosine kinases.<br \/>\n<em>Tetrahedron<\/em>\u00a0<strong>2018<\/strong>, <em>74<\/em>, 1802\u20131809.<br \/>\n<a href=\"https:\/\/doi.org\/10.1016\/j.tet.2018.02.042\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1016\/j.tet.2018.02.042<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kaneda, M.; Inuki, S.; Ohno, H.; Oishi, S.<br \/>\nTotal Synthesis and Stereochemical Revision of Stereocalpin A: Mirror-Image Approach for Stereochemical Assignments of the Peptide\u2013Polyketide Macrocycle.<br \/>\n<em>J. Org. Chem.<\/em> <strong>2018<\/strong>, <em>83<\/em>, 3047\u20133060.<br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.8b00118\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.joc.8b00118<\/span><\/a><\/span><\/div>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2017\"><\/a>2017<\/span><\/h4>\n<ol>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kode, J.; Khattry, N.; Bakshi, A.; Amrutkar, V.; Bagal, B.; Karandikar, R.; Rane, P.; Fujii, N.; Chiplunkar, S.<br \/>\nStudy of stem cell homing &amp; self-renewal marker gene profile of ex vivo expanded human CD34+ cells manipulated with a mixture of cytokines &amp; stromal cell-derived factor 1<br \/>\n<em>Indian. J. Med. Res<\/em>. <strong>2017<\/strong>, <em>146<\/em>, 56\u201370.<br \/>\n<a href=\"https:\/\/doi.org\/10.4103\/ijmr.IJMR_1319_15\" class=\"liinternal\"><span style=\"color: #3366ff\"><span style=\"font-family: tahoma, arial, helvetica, sans-serif\">DOI: <\/span><\/span><\/a><\/span><\/span><span class=\"identifier doi\" style=\"font-family: tahoma, arial, helvetica, sans-serif;color: #3366ff\">10.4103\/ijmr.IJMR_1319_15<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kobayashi, Y.; Kameda, T.; Hoshino, M.; Fujii, N.; Ohno, H.; Oishi, S.<br \/>\nFe(II)-Complexation of tripodalhexapeptide ligands with three bidentate triazolylpyridines: induction of metal-centred chirality by peptide macrocyclization.<br \/>\n<em>Dalton Trans<\/em>.\u00a0<strong>2017<\/strong>, <em>46<\/em>, 13673\u201313676.<br \/>\n<a href=\"https:\/\/doi.org\/10.1039\/C7DT02739G\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1039\/C7DT02739G<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nakamura, S.; Ito, Y.; Yamamoto, K.; Takahashi, C.; Dai, M.; Tanahashi, M.; Uenoyama, Y.; Tsukamura, H.; Oishi, S.; Maeda, K.; Matsuda, F.<br \/>\nSB223412, a neurokinin-3 receptor-selective 1 antagonist, suppresses testosterone secretion in male guinea pigs.<br \/>\n<em>Theriogenology<\/em>\u00a0<strong>2017<\/strong>, <em>102<\/em>, 183\u2013189.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.theriogenology.2017.07.053\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.theriogenology.20<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shu, K.; Noguchi, T.; Honda, K.; Kondoh, Y.; Osada, H.; Ohno, H.; Fujii, N.; Oishi, S.<br \/>\nSynthesis of the Src SH2 domain and its application in bioassays for mirror-image screening.<br \/>\n<em>RSC Adv.<\/em>\u00a0<strong>2017<\/strong>, <em>7<\/em>, 38725\u201338732.<br \/>\n<a href=\"https:\/\/doi.org\/10.1039\/C7RA07445J\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1039\/C7RA07445J<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Hamada N.; Yoshida Y.; Oishi S.; Ohno H.<\/span><br \/>\n<span style=\"font-size: 12pt\">Gold-Catalyzed Cascade Reaction of Skipped Diynes for the Construction of a Cyclohepta[b]pyrrole Scaffold.<\/span><br \/>\n<span style=\"font-size: 12pt\"><em>Org. Lett.<\/em>\u00a0<strong>2017<\/strong>, <em>19<\/em>, 3875\u20133878.<br \/>\n<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.7b01759\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1021\/acs.orglett.7b01759<\/span><\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuoka, J.; Matsuda, Y.; Kawada, Y.; Oishi, S.; Ohno H.<br \/>\nTotal Synthesis of Dictyodendrins by the Gold-Catalyzed Cascade Cyclization of Conjugated Diynes with Pyrroles.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em>\u00a0<strong>2017<\/strong>, <em>56<\/em>, 7444\u20137448.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.201703279\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.201703279<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ikegami, K.; Minabe, S.; Ieda, N.; Goto, T.; Sugimoto, A.; Nakamura, S.; Inoue, N.; Oishi, S. Maturana, A. D.; Sanbo, M.; Hirabayashi, M.; Maeda, K.-I.; Tsukamura, H.; Uenoyama, Y.<br \/>\nEvidence of involvement of neurone-glia\/neurone-neurone communications via gap junctions in synchronised activity of KNDy neurones.<br \/>\n<em>J. Neuroendocrinol.<\/em>\u00a0<strong>2017<\/strong>, 29.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1111\/jne.12480\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1111\/jne.12480<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ishiba, H.; Noguchi, T.; Shu, K.; Ohno, H.; Honda, K.; Kondoh, Y.; Osada, H.; Fujii, N.; Oishi, S.<br \/>\nInvestigation of the inhibitory mechanism of apomorphine against MDM2\u2013p53 interaction.<br \/>\n<em>Bioorg. Med. Chem. Lett.<\/em>\u00a0<strong>2017<\/strong>, <em>27<\/em>, 2571\u20132574.<br \/>\n<a href=\"https:\/\/doi.org\/10.1016\/j.bmcl.2017.03.082\" class=\"liinternal\"><span style=\"color: #3366ff\">DOI: 10.1016\/j.bmcl.2017.03.082<\/span><\/a><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ohno, H.; Honda, M.; Hamada, N.; Miyagaki, J.; Iwata, A.; Otsuki, K.; Maruyama, T.; Nakamura, A.; Nakanishi, I.; Inuki, S.; Fujii, N.; Oishi, S.<br \/>\nIdentification of selective inhibitors of sphingosine kinases 1 and 2 through a structure\u2013activity relationship study of 4-<em>epi<\/em>-jaspine B.<br \/>\n<em>Bioorg. Med. Chem.<\/em>\u00a0<strong>2017<\/strong>, <em>25<\/em>, 3046\u20133052.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1016\/j.bmc.2017.03.059\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1016\/j.bmc.2017.03.059<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Noguchi, T.; Ishiba, H.; Honda, K.; Kondoh, Y.; Osada, H.; Ohno, H.; Fujii, N.; Oishi, S.<br \/>\nSynthesis of Grb2 SH2 Domain Proteins for Mirror-Image Screening Systems.<br \/>\n<em>Bioconjug. Chem.<\/em>\u00a0<strong>2017<\/strong>, <em>28<\/em>, 609\u2013619.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.6b00692\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1021\/acs.bioconjchem.6b00692<\/a><\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yano, Y.; Kondo, K.; Watanabe, Y.; Zhang, T. O.; Ho, J. J.; Oishi, S.; Fujii, N.; Zanni, M. T.; Matsuzaki, K.<br \/>\nGXXXG-mediated parallel and antiparallel dimerization of transmembrane helices and its inhibition by cholesterol: single-pair FRET and 2D IR studies.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em> <strong>2017<\/strong>, <em>56<\/em>, 1756\u20131759.<br \/>\n<span style=\"color: #3366ff\"><a href=\"https:\/\/doi.org\/10.1002\/anie.201609708\" style=\"color: #3366ff\" class=\"liinternal\">DOI: 10.1002\/anie.201609708<\/a><\/span><\/span><\/div>\n<\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2016\"><\/a>2016<\/span><\/h4>\n<ol>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Alam, M.; Kuwata, T.; Shimura, K.; Yokoyama, M.; Ramirez Valdez, K. P.; Tanaka, K.; Maruta, Y.; Oishi, S.; Fujii, N.; Sato, H.; Matsuoka, M.; Matsushita, S.<br \/>\nEnhanced antibody-mediated neutralization of HIV-1 variants that are resistant to fusion inhibitors.<br \/>\nRetrovirology.\u00a0<b>13<\/b>(1), 70, (2016)<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sawada, J.; Osawa, A.; Takeuchi, T.; Kaneda, M.; Oishi, S.; Fujii, N.; Asai, A.; Tanino, K.; Namba, K.<br \/>\nFunctional 1,3a,6a-triazapentalene scaffold: Design of fluorescent probes for kinesin spindle protein (KSP).<br \/>\nBioorg. Med. Chem. Lett.\u00a0<b>26<\/b>(23) 5765-5769. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Watanabe, M.; Hashimoto, K.; Abe, Y.; Kodama, E.N.; Nabika, R.; Oishi, S.; Ohara, S.; Sato, M.; Kawasaki, Y.; Fujii, N.; Hosoya, M.<br \/>\nA novel peptide derived from the fusion protein heptad repeat inhibits replication of subacute sclerosing panencephalitis virus in vitro and in vivo.<br \/>\nPLoS One.\u00a0<b>11<\/b>(9) e0162823.\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Hattori, Y.; Machida,Y.;Honda, M.;Ohno, H.;Fujii, N.;Onishi, H.<br \/>\nSmall interfering RNA delivery into the liver by cationic cholesterol derivative-based liposomes.<br \/>\nJ. Liposome Res. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Suzuki, T.; Nojo, W.; Sakano, Y.; Katoono, R.; Ishigaki, Y.; Ohno, H.; Fujiwara, K.<br \/>\nRedox-induced conformational changes in 1,3-propylene- and m-xylylenebis[5-(10-butyl-5,10-dihydrobenzo[a]indolo[2,3-c]carbazole)]: twin-BIC donors that form sandwich-like dimeric cations exhibiting NIR absorption.<br \/>\nChem. Lett.\u00a0<b>45<\/b>(7) 720-722. (2016)<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kaneda, M.; Sueyoshi, K.; Teruya, T.; Ohno, H.; Fujii, N.; Oishi, S.<br \/>\nTotal synthesis of odoamide, a novel cyclic depsipeptide from an Okinawan marine cyanobacterium.<br \/>\nOrg. Biomol. Chem.\u00a0<b>14<\/b>(38) 9093-9104. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Abdelouahab, H.; Zhang, Y.; Wittner, M.; Oishi, S.; Fujii, N.; Besancenot, R.; Plo, I.; Ribrag, V.; Solary, E.; Vainchenker, W.; Barosi, G.; Louache, F.<br \/>\nCXCL12\/CXCR4 pathway is activated by oncogenic JAK2 in a PI3K-dependent manner.<br \/>\nOncotarget, DOI: 10.18632\/oncotarget.10789.\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sueyoshi, K.; Kaneda, M.; Sumimoto, S.; Oishi, S.; Fujii, N.; Suenaga, K.; Teruya, T.<br \/>\nOdoamide, a cytotoxic cyclodepsipeptide from the marine cyanobacterium Okeania sp.<br \/>\nTetrahedron,\u00a0<b>72<\/b>(35) 5472-5478. (2016)<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Naoe, S.; Yoshida, Y.; Oishi, S.; Fujii, N.; Ohno, H.<\/span><br \/>\n<span style=\"font-size: 12pt\">Total synthesis of (+)-conolidine by the gold(I)-catalyzed cascade cyclization of a conjugated enyne.<\/span><br \/>\n<span style=\"font-size: 12pt\">J. Org. Chem.\u00a0<b>81<\/b>(13) 5690-5698. (2016)\u00a0<\/span><\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yamamoto, K.; Okazaki, S.; Ohno, H.; Matsuda, F.; Ohkura, S.; Maeda, K.; Fujii, N.; Oishi, S.<br \/>\nDevelopment of novel NK3 receptor antagonists with reduced environmental impact.<br \/>\nBioorg. Med. Chem.\u00a0<b>24<\/b>(16) 3494-3500. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Noguchi, T.; Oishi, S.; Honda, K.; Kondoh, Y.; Saito, T.; Ohno, H.; Osada, H.; Fujii, N.<br \/>\nScreening of a virtual mirror-image library of natural products.<br \/>\nChem. Commun.\u00a0<b>52<\/b>(49) 7653-7656. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kato, F.; Ishida, Y.; Oishi, S.; Fujii, N.; Watanabe, S.; Vasudevan, S. G.; Tajima, S.; Takasaki, T.; Suzuki, Y.; Ichiyama, K.; Yamamoto, N.; Yoshii, K.; Takashima, I.; Kobayashi, T.; Miura, T.; Igarashi, T.; Hishiki, T.<br \/>\nNovel antiviral activity of bromocriptine against dengue virus replication.<i><i><br \/>\nAntiviral Res.\u00a0<\/i><\/i><b>131<\/b> 141-147. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nishiyama, D.; Sakai, Y.; Sekiguchi, H.; Chiba, H.; Misu, R.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nNovel 3,4,7-substituted benzofuran derivatives having binding affinity to \u03ba-opioid receptor.<br \/>\nChem. Pharm. Bull.\u00a0<b>64<\/b>(7) 996-1003. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nishiyama, D.; Ohara, A.; Chiba, H.; Kumagai, H.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nFormal total synthesis of (\u00b1)-strictamine based on a gold-catalyzed cyclization.<br \/>\nOrg. Lett.\u00a0<b>18<\/b>(7) 1670-1673. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Ohno, H.; Minamiguchi, D.; Nakamura, S.; Shu, K.; Okazaki, S.; Honda, M.; Misu, R.; Moriwaki, H.; Nakanishi, S.; Oishi, S.; Kinoshita, T.; Nakanishi, I.; Fujii, N.<br \/>\nStructure-activity relationship study of 4-(thiazol-5-yl)benzoic acid derivatives as potent protein kinase CK2 inhibitors.<br \/>\nBioorg. Med. Chem.\u00a0<b>24<\/b>(5) 1136-1141. (2016)\u00a0<\/span><\/li>\n<li><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Wagner, B.; Hiller, W.; Ohno, H.; Krause, N.<br \/>\nGold-catalyzed three-component spirocyclization: a one-pot approach to functionalized pyrazolidines.<br \/>\nOrg. Biomol. Chem.\u00a0<b>14<\/b>(5) 1579-1583. (2016)\u00a0<\/span><\/li>\n<\/ol>\n<h4><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 14pt\"><a id=\"link2015\"><\/a>2015<\/span><\/h4>\n<ol class=\"font\">\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shi, J.; Liu, N.; Xiao, Y.; Takei, Y.; Yasue, M.; Suzuki, Y.; Hou, Z.; Ohno, H.; Tsujimoto, G.; Hirasawa, A.<i><i><br \/>\n<\/i><\/i>The effects of a selective CK2 inhibitor on anti-glomerular basement membrane glomerulonephritis in rats.<br \/>\n<em>Biol. Pharm. Bull<\/em>.\u00a0<b>38<\/b>(9) 1345\u20131351. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Miyamoto, F.; Kawaji, K.; Oishi, S.; Fujii, N.; Kaku, M.; Kodama, E. N.<br \/>\nAnti-HIV-1 activity determined by \u03b2-galactosidase activity in the multinuclear activation of an indicator assay is comparable with that by a conventional focus counting method.<br \/>\n<em>Antivir. Chem. Chemother<\/em>.\u00a0<b>24<\/b> 77\u201382. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Taguchi, M.; Tokimizu, Y.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nSynthesis of fused carbazoles by gold-catalyzed tricyclization of conjugated diynes via rearrangement of an \u039d-propargyl group.<br \/>\nOrg. Lett.\u00a0<b>17<\/b>(24) 6250\u20136253. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Umatani, C.; Misu, R.; Oishi, S.; Yamaguchi, K.; Abe, H.; Oka, Y.<br \/>\nGnRH suppresses excitability of visual-processing neurons in the optic tectum.<br \/>\n<em>J<\/em>. <em>Neurophysiol.<\/em>\u00a0<b>114<\/b>(5) 2775\u20132784. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Shimura, K.; Miyazato, P.; Oishi, S.; Fujii, N.; Matsuoka, M.<i><i><br \/>\n<\/i><\/i>Impact of HIV-1 infection pathways on susceptibility to antiviral drugs and on virus spread.<br \/>\n<em>Virology<\/em>\u00a0<b>484<\/b> 364\u2013376. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Oishi, S.; Kuroyanagi, T.; Kubo, T.; Montpas, N.; Yoshikawa, Y.; Misu, R.; Kobayashi, Y.; Ohno, H.; Heveker, N.; Furuya, T.; Fujii, N.<br \/>\nDevelopment of novel CXC chemokine receptor 7 (CXCR7) ligands: selectivity switch from CXCR4 antagonists with a cyclic pentapeptide scaffold.<br \/>\n<em>J<\/em>. <em>Med<\/em>. <em>Chem<\/em>.\u00a0<b>58<\/b>(13) 5218\u20135225. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Iwata, A.; Inuki, S.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\n<\/span><\/span><\/div>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">C<\/span><span style=\"font-size: 12pt\">onvenient synthesis of spiroindole derivatives via palladium-catalyzed cyclization of propargyl chlorides.<br \/>\n<\/span><span style=\"font-size: 12pt\"><em>Tetrahedron<\/em> <b>71<\/b>(37) 6580\u20136585. (2015)<\/span><b><br \/>\n<\/b><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Takenaga, M.; Yamamoto, Y.; Takeuchi, T.; Ohta, T; Tokura, Y.; Hamaguchi, A.; Asai, D.; Nakashima, H.; Oishi, S.; Fujii, N.<br \/>\nPotential new chemotherapy strategy for human ovarian carcinoma with a novel KSP inhibitor.<br \/>\nBiochem. Biophys. Res. Commun.\u00a0<b>463<\/b>(3) 222\u2013228. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tokimizu, Y.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nGold-catalyzed cascade cyclization of 2-alkynyl-N-propargylanilines via the rearrangement of a propargyl group.<br \/>\nAngew. Chem. Int. Ed.\u00a0<b>54<\/b>(27) 7862\u20137866. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Naoe, S.; Saito, T.; Uchiyama, M.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nDirect construction of fused indoles by gold-catalyzed cascade cyclization of conjugated diynes.<br \/>\nOrg. Lett.\u00a0<b>17<\/b>(7) 1774\u20131777. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Yasuda, Y.; Arakawa, T.; Nawata, Y.; Shimada, S.; Oishi, S.; Fujii, N.; Nishimura, S.; Hattori, A.; Kakeya, H.<br \/>\nDesign, synthesis, and structure-activity relationships of 1-ethylpyrazole-3-carboxamide compounds as novel hypoxia-inducible factor (HIF)-1 inhibitors.<i><i><br \/>\nBioorg. Med. <\/i><\/i>Chem.\u00a0<b>23<\/b>(8) 1776\u20131787. (2015)<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Montpas, N.; Cabana, J.; St-Onge, G.; Gravel, S.; Morin, G.; Kuroyanagi, T.; Lavigne, P.; Fujii, N.; Oishi, S.; Heveker, N.<br \/>\nThe binding mode of the cyclic agonist peptide TC14012 to CXCR7 - Identification of receptor and compound determinants.<br \/>\nBiochemistry\u00a0<b>54<\/b>(7) 1505\u20131515. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Okazaki, S.; Oishi, S.; Mizuhara, T.; Shimura, K.; Murayama, H.; Ohno, H.; Matsuoka, M.; Fujii, N.<br \/>\nInvestigations of possible prodrug structures for 2-(2-mercaptophenyl)tetrahydropyrimidines: reductive conversion from anti-HIV agents with pyrimidobenzothiazine and isothiazolopyrimidine scaffolds.<br \/>\nOrg. Biomol. Chem.\u00a0<b>13<\/b>(16) 4706\u20134713. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Hattori, Y.; Hara, E.; Shingu, Y.; Minamiguchi, D.; Nakamura, A.; Arai, S.; Ohno, H.; Kawano, K.; Fujii, N.; Yonemochi, E.<\/span><br \/>\n<span style=\"font-size: 12pt\">siRNA delivery into tumor cells by cationic cholesterol derivative-based nanoparticles and liposomes.<\/span><br \/>\n<span style=\"font-size: 12pt\">Biol. Pharm. Bull.\u00a0<b>38<\/b>(1) 30\u201338. (2015)<\/span><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Okazaki, S.; Mizuhara, T.; Shimura, K.; Murayama, H.; Ohno, H.; Oishi, S.; Matsuoka, M.; Fujii, N.<br \/>\nIdentification of anti-HIV agents with a novel benzo[4,5]isothiazolo[2,3-a]pyrimidine scaffold.<br \/>\nBioorg. Med. Chem.\u00a0<b>23<\/b>(7) 1447\u20131452. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Kawabata, H.; Uchiyama, T.; Sakamoto, S.; Kanda, J.; Oishi, S.; Fujii, F.; Tomosugi, N.; Kadowaki, N.; Takaori-Kondo, A.<br \/>\nA HAMP promoter bioassay system for identifying chemical compounds that modulate hepcidin expression.<br \/>\nExp. Hematol.\u00a0<b>43<\/b>(5) 404\u2013413. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tokimizu, Y.; Wieteck, M.; Rudolph, M.; Oishi, S.; Fujii, N.; Hashmi, A. S. K.; Ohno, H.<i><i><br \/>\n<\/i><\/i>Dual gold catalysis: a novel synthesis of bicyclic and tricyclic pyrroles from N-propargyl ynamides.<br \/>\nOrg. Lett.\u00a0<b>17<\/b>(3) 604\u2013607. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Misu, R.; Yamamoto, K.; Yamada, A.; Noguchi, T.; Ohno, H.; Yamamura, T.; Okamura, H.; Matsuda, F.; Ohkura, S.; Oishi, S.; Fujii, N.<br \/>\nStructure-activity relationship study on senktide for development of novel potent neurokinin-3 receptor selective agonists.<br \/>\nMedChemCommun.\u00a0<b>6<\/b>(3) 469\u2013476. (2015)<b><\/b><\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tsunematsu, Y.; Nishimura, S.; Hattori, A.; Oishi, S.; Fujii, N.; Kakeya, H.<br \/>\nIsolation, structure elucidation and total synthesis of tryptopeptins A and B, new TGF-beta signaling modulators from Streptomyces sp.<br \/>\nOrg. Lett.\u00a0<b>17<\/b>(2) 258\u2013261. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nabika, R.; Suyama, T. L.; Hau, A. M.; Misu, R.; Ohno, H.; Ishmael, J. E.; McPhail, K. L.; Oishi, S.; Fujii, N.<br \/>\nSynthesis and biological evaluation of the [D-MeAla11]-epimer of coibamide A.<br \/>\nBioorg. Med. Chem. Lett.\u00a0<b>25<\/b>(2) 302\u2013306. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Matsuda, Y.; Naoe, S.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nFormal [4+2] reaction between 1,3-diynes and pyrroles: gold(I)-catalyzed indole synthesis by double hydroarylation.<br \/>\n<em>Chem. Eur. J.<\/em>\u00a0<b>21<\/b>(4) 1463\u20131467. (2015)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif\"><span style=\"font-size: 12pt\">Zenda, M.; Yasui, H.; Oishi, S.; Masuda, R.; Fujii, N.; Koide, T.<br \/>\n<\/span><\/span><span style=\"font-size: 12pt\">A cisplatin derivative that inhibits collagen fibril-formation in vitro.<br \/>\n<\/span><span style=\"font-size: 12pt\"><em>Chem. Biol. Drug Des<\/em>.\u00a0<b>85<\/b>(5) 519\u2013526. 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(2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Nabika, R.; Oishi, S.; Misu, R.; Ohno, H.; Fujii, N.<br \/>\nSynthesis of IB-01212 by multiple N-methylations of peptide bonds.<br \/>\nBioorg. Med. Chem.\u00a0<b>22<\/b>(21) 6156-6162. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tokimizu, Y.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nGold-catalyzed cascade cyclization of (azido)ynamides: an efficient strategy for the construction oflndoloquinolines.<br \/>\nOrg. Lett.\u00a0<b>16<\/b>(11) 3138-3141. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Tsutsui, A.; Imamaki, R.; Kitazume, S.; Hanashima, S.; Yamaguchi, Y.; Kaneda, M.; Oishi, S.; Fujii, N.; Taniguchi, N.; Tanaka, K.<br \/>\nPolyamine modification by acrolein exclusively produces 1,5-diazacyclooctanes: a previously unrecognized mechanism for acrolein-mediated oxidative stress.<i><i><br \/>\n<\/i><\/i>Org. Biomol. Chem.\u00a0<b>12<\/b>(28) 5151-5157. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Suzuki, T.; Sakano, Y.; Tokimizu, Y.; Miura, Y.; Katoono, R.; Fujiwara, K.; Yoshioka, N.; Fujii, N.; Ohno, H.<br \/>\nWurster's blue-type cation radicals framed in a 5,10-dihydrobenzo[a]indolo[2,3-c]carbazole (BIC) skeleton: dual electrochromism with drastic changes in UV-Vis-NIR and fluorescence.<br \/>\nChem. Ajian J.\u00a0<b>9<\/b>(7) 1841-1846. 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(2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Takeuchi, T.; Oishi, S.; Kaneda, M.; Misu, R.; Ohno, H.; Sawada, J.; Asai, A.; Nakamura, S.; Nakanishi, I.; Fujii, N.<br \/>\nOptimization of diaryl amine derivatives as kinesin spindle protein inhibitors.<br \/>\nBioorg. Med. Chem.\u00a0<b>22<\/b>(12) 3171-3179. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Takeuchi, T.; Oishi, S.; Kaneda, M.; Ohno, H.; Nakamura, S.; Nakanishi, I.; Yamane, M.; Sawada, J.; Asai, A.; Fujii, N.<br \/>\nKinesin spindle protein inhibitors with diaryl amine scaffolds: crystal packing analysis for improved aqueous solubility.<br \/>\nACS Med. Chem. Lett.\u00a0<b>5<\/b>(5) 566-571. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Sano, K.; Masuda, R.; Hisada,H.; Oishi, S.; Shimokawa, K.; Ono, M.; Fujii, N.; Saji, H.; Mukai, T.<br \/>\nA radiogallium-DOTA-based bivalent peptidic ligand targeting a chemokine receptor, CXCR4, for tumor imaging.<br \/>\nBioorg. Med. Chem. Lett.\u00a0<b>24<\/b>(5) 1386-1388. (2014)\u00a0<\/span><\/div>\n<\/li>\n<li>\n<div><span style=\"font-family: tahoma, arial, helvetica, sans-serif;font-size: 12pt\">Iwata, A.; Inuki, S.; Oishi, S.; Fujii, N.; Ohno, H.<br \/>\nSynthesis of fused tetracyclic spiroindoles via palladium-catalysed cascade cyclisation.<i><i><br \/>\nChem. Commun.<\/i><\/i> <strong>2014<\/strong>, <em>50<\/em>, 298\u2013300.<\/span><\/div>\n<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>[2026][2025][2024][2023][2022][2021][2020][2019][2018][2017][2016][2015] [2014] [2013\u4ee5\u524d] 2026 Fujii, T.; Araki [&hellip;]<\/p>\n","protected":false},"author":47,"featured_media":0,"parent":0,"menu_order":18,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-219","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/pages\/219","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/users\/47"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=219"}],"version-history":[{"count":6,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/pages\/219\/revisions"}],"predecessor-version":[{"id":2736,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=\/wp\/v2\/pages\/219\/revisions\/2736"}],"wp:attachment":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/souyaku\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=219"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}