{"id":145,"date":"2013-06-18T14:16:15","date_gmt":"2013-06-18T05:16:15","guid":{"rendered":"http:\/\/www.keyton-co.jp\/kpharm\/byotai\/?page_id=145"},"modified":"2025-03-24T18:20:24","modified_gmt":"2025-03-24T09:20:24","slug":"research10","status":"publish","type":"page","link":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/theme-list\/molecular-imaging\/research10\/","title":{"rendered":"\u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u8a3a\u65ad\u306e\u305f\u3081\u306e\u5206\u5b50\u30d7\u30ed\u30fc\u30d6\u958b\u767a\u2460"},"content":{"rendered":"<h2><strong>\u03b2\u30a2\u30df\u30ed\u30a4\u30c9\u30bf\u30f3\u30d1\u30af\u8cea\u6a19\u7684\u30d7\u30ed\u30fc\u30d6<\/strong><\/h2>\n<p><span style=\"color: #000000\">\u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u60a3\u8005\u8133\u5185\u306b\u304a\u3051\u308b\u4e3b\u306a\u75c5\u7406\u5b66\u7684\u5909\u5316\u3068\u3057\u3066\u3001\u03b2\u30a2\u30df\u30ed\u30a4\u30c9\u30bf\u30f3\u30d1\u30af\u8cea(A\u03b2)\u3092\u4e3b\u69cb\u6210\u6210\u5206\u3068\u3059\u308b\u8001\u4eba\u6591\u306e\u6c88\u7740\u3068\u3001\u904e\u5270\u30ea\u30f3\u9178\u5316\u3055\u308c\u305f\u30bf\u30a6\u30bf\u30f3\u30d1\u30af\u8cea\u3092\u4e3b\u6210\u5206\u3068\u3059\u308b\u795e\u7d4c\u539f\u7dda\u7dad\u5909\u5316(NFT)\u304c\u77e5\u3089\u308c\u3066\u3044\u308b\u3002A\u03b2\u306e\u6c88\u7740\u306f\u3001\u8a18\u61b6\u30fb\u8a8d\u77e5\u6a5f\u80fd\u306e\u4f4e\u4e0b\u306a\u3069\u306e\u81e8\u5e8a\u75c7\u72b6\u304c\u51fa\u73fe\u3059\u308b\u4ee5\u524d\u304b\u3089\u59cb\u307e\u308b\u3053\u3068\u3001\u307e\u305f\u75be\u60a3\u7279\u7570\u6027\u304c\u9ad8\u3044\u3053\u3068\u304b\u3089AD\u306e\u65e9\u671f\u304a\u3088\u3073\u4ed6\u306e\u75be\u60a3\u3068\u306e\u9451\u5225\u8a3a\u65ad\u306b\u3064\u306a\u304c\u308b\u3068\u3055\u308c\u3066\u304d\u305f\u3002\u305d\u306e\u305f\u3081\u3001A\u03b2\u51dd\u96c6\u4f53\u3092\u6a19\u7684\u3068\u3057\u305f\u653e\u5c04\u6027\u30d7\u30ed\u30fc\u30d6\u306e\u958b\u767a\u7814\u7a76\u3092\u884c\u306a\u3063\u3066\u3044\u308b\u3002<\/span><\/p>\n<p><a href=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb.png\" class=\"liimagelink\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2297\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb.png\" alt=\"\" width=\"720\" height=\"540\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb.png 720w, https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb-300x225.png 300w\" sizes=\"auto, (max-width: 720px) 100vw, 720px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc.jpg\" class=\"liimagelink\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2301\" src=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc.jpg\" alt=\"\" width=\"1500\" height=\"1125\" srcset=\"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc.jpg 1500w, https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc-300x225.jpg 300w, https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc-768x576.jpg 768w, https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/files\/2018\/08\/A\u03b2\u7d39\u4ecb2\u306e\u30b3\u30d4\u30fc-1024x768.jpg 1024w\" sizes=\"auto, (max-width: 1500px) 100vw, 1500px\" \/><\/a><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<h3>\u4e3b\u8981\u8ad6\u6587<\/h3>\n<ul>\n<li><span class=\"Apple-style-span\">Core Binding Site of a Thioflavin-T-derived Imaging Probe on Amyloid \u03b2 Fibrils Predicted by Computational Methods<br \/>\n<em>ACS Chem. Neurosci.<\/em>\u00a09(5) 957-966 (2018)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Development of Novel\u00a0<sup>123<\/sup>I-Labeled Pyridyl Benzofuran\u00a0Derivatives for SPECT Imaging of \u03b2-Amyloid Plaques in Alzheimer\u2019s Disease<br \/>\n<em>PLoS ONE<\/em>\u00a08\u00a0(9) e74104 (2013)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Novel\u00a0<sup>18<\/sup>F-labeled benzoxazole derivatives as potential positron emission tomography probes for imaging of cerebral \u03b2-amyloid plaques in alzheimers disease<br \/>\n<em>J. Med. Chem.<\/em>\u00a055\u00a0(21) 9136-9145 (2012)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Technetium-99m labeled pyridyl benzofuran derivatives as single photon emission computed tomography imaging probes for \u03b2-amyloid plaques in Alzheimer\u2019s brains<br \/>\n<em>J. Med. Chem.<\/em>\u00a055\u00a0(5) 2279-2286 (2012)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Novel\u00a0<sup>18<\/sup>F-labeled benzofuran derivatives with improved properties for positron emission tomography (PET) imaging of \u03b2-amyloid plaques in Alzheimer\u2019s brains<br \/>\n<em>J. Med. Chem.<\/em>\u00a054\u00a0(8) 2971-2979 (2011)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Synthesis and structure-affinity relationships of novel dibenzylideneacetone derivatives as probes for \u03b2-Amyloid Plaques<br \/>\n<em>J. Med. Chem.<\/em>\u00a054\u00a0(7) 2225-2240 (2011)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Synthesis and evaluation of novel chalcone derivatives with <sup>99m<\/sup>Tc\/Re complexes as potential probes for detection of \u03b2-amyloid plaques.<br \/>\n<em>ACS Chem. Neurosci.<\/em> 1\u00a0(9) 598-607 (2010)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Novel radioiodinated aurones as probes for SPECT imaging of \u03b2-amyloid plaques in the brain.<br \/>\n<em>Bioconjug. Chem.<\/em> 20 (1) 95-101 (2009)\u00a0<\/span><\/li>\n<li><span class=\"Apple-style-span\">Fluoro-pegylated chalcones as positron emission tomography probes for in vivo imaging of \u03b2-amyloid plaques in Alzheimer&#8217;s disease.<br \/>\n<em>J Med. Chem.<\/em> 52 (20) 6394-401 (2009)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Novel benzofuran derivatives for PET imaging of \u03b2-amyloid plaques in Alzheimer&#8217;s disease brains.<br \/>\n<em>J. Med. Chem.<\/em> 49 2725-2730 (2006)<\/span><\/li>\n<li><span class=\"Apple-style-span\">Radioiodinated flavones for in vivo imaging of \u03b2-amyloid plaques in the brain.<br \/>\n<em>J. Med. Chem.<\/em> 48 7253-7260 (2005)<\/span><\/li>\n<li><sup>11<\/sup>C-labeled stilbene derivatives as A\u03b2-aggregate-specific PET imaging agents for Alzheimer\u2019s disease.<br \/>\n<em>Nucl. Med. Biol.<\/em> 30\u00a0565-571 (2003)<\/li>\n<\/ul>\n<h3>\u7dcf\u8aac\u7b49<\/h3>\n<ul>\n<li><span style=\"font-size: 14px;text-indent: 1em\">Recent Advances in Molecular Imaging Probes for \u03b2-Amyloid Plaques<\/span>,<br \/>\n<span style=\"font-size: 14px\"><em>Med. Chem. Commun<\/em>. <\/span>6<span style=\"font-size: 14px\">(3) 391-402 (2015)<\/span><\/li>\n<li>SPECT imaging agents for detecting cerebral \u03b2-amyloid plaques.<br \/>\n<span style=\"font-size: 14px\"><em>International Journal of Molecular Imaging<\/em>, Article ID 543267, doi:10.1155\/2011\/543267 (2011)<\/span><\/li>\n<li>PET\/SPECT imaging agents for detecting of cerebral \u03b2-amyloid plaques.<br \/>\n<span style=\"font-size: 14px\"><em>Cognition and Dementia<\/em>, 9, 13-18 (2010)<\/span><\/li>\n<li>\u5e73\u621021\u5e743\u67081\u65e5\u767a\u520a\u3001\u533b\u85ac\u30fb\u751f\u547d\u79d1\u5b66\u8a8c\u300c\u30e1\u30c7\u30a3\u30ab\u30eb\u30d0\u30a4\u30aa\u30002009\u5e743\u6708\u53f7\u300d\uff08p.84-87\uff09\u3001\u300c\u7b2c11\u56de\u5148\u99c6\u8005\u30d7\u30ec\u30ab\u30fc\u30b5\u30fc\uff1a\u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u306e\u65e9\u671f\u8a3a\u65ad\u3092\u53ef\u80fd\u306b\u3059\u308b\u30a2\u30df\u30ed\u30a4\u30c9\u03b2\u691c\u51fa\u30d7\u30ed\u30fc\u30d6\u306e\u958b\u767a\u300d<\/li>\n<li>PET\/SPECT\u306b\u3088\u308b\u5206\u5b50\u30a4\u30e1\u30fc\u30b8\u30f3\u30b0\u7814\u7a76\u3001<br \/>\n<em>\u85ac\u5b66\u96d1\u8a8c<\/em>. 129(3) 279-287 (2009)<\/li>\n<li>Development of positron-emission tomography\/single-photon emission computed tomography imaging probes for in vivo detection of \u03b2-amyloid plaques in Alzheimer&#8217;s brains.<br \/>\n<em>Chem Pharm Bull (Tokyo)<\/em>. \u00a057(10)1029-1039 (2009)<\/li>\n<li>PET\/SPECT\u306b\u3088\u308b\u03b2\u30a2\u30df\u30ed\u30a4\u30c9\u306e\u5206\u5b50\u30a4\u30e1\u30fc\u30b8\u30f3\u30b0\uff5e\u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u306e\u65e9\u671f\u8a3a\u65ad\u3092\u76ee\u6307\u3057\u3066<br \/>\n<em>\u5316\u5b66<\/em>, 63, 64-65 (2008)<\/li>\n<li>PET\/SPECT\u3092\u7528\u3044\u305f\u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u306e\u753b\u50cf\u8a3a\u65ad\u3001<br \/>\n<em>\u85ac\u5264\u5b66<\/em>\u300168, 209-216 (2008)<\/li>\n<li>Molecular imaging of \u03b2-amyloid plaques in the brain.<br \/>\n<em>Brain Nerve<\/em>, 59, 233-240 (2007)<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>\u03b2\u30a2\u30df\u30ed\u30a4\u30c9\u30bf\u30f3\u30d1\u30af\u8cea\u6a19\u7684\u30d7\u30ed\u30fc\u30d6 \u30a2\u30eb\u30c4\u30cf\u30a4\u30de\u30fc\u75c5\u60a3\u8005\u8133\u5185\u306b\u304a\u3051\u308b\u4e3b\u306a\u75c5\u7406\u5b66\u7684\u5909\u5316\u3068\u3057\u3066\u3001\u03b2\u30a2\u30df\u30ed\u30a4\u30c9\u30bf\u30f3\u30d1\u30af\u8cea(A\u03b2)\u3092\u4e3b\u69cb\u6210\u6210\u5206\u3068\u3059\u308b\u8001\u4eba\u6591\u306e\u6c88\u7740\u3068\u3001\u904e\u5270\u30ea\u30f3\u9178\u5316\u3055\u308c\u305f\u30bf\u30a6\u30bf\u30f3\u30d1\u30af\u8cea\u3092\u4e3b\u6210\u5206\u3068\u3059\u308b\u795e\u7d4c\u539f\u7dda\u7dad\u5909\u5316(N [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":133,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-145","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/145","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/comments?post=145"}],"version-history":[{"count":5,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/145\/revisions"}],"predecessor-version":[{"id":3256,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/145\/revisions\/3256"}],"up":[{"embeddable":true,"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/pages\/133"}],"wp:attachment":[{"href":"https:\/\/www.pharm.kyoto-u.ac.jp\/byotai\/wp-json\/wp\/v2\/media?parent=145"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}