Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376619 | Bioorganic & Medicinal Chemistry Letters | 2008 | 4 Pages |
Abstract
Structure–activity studies on benzimidazole lead 1 obtained from library screening led to the discovery of potent and selective ORL1 antagonist 28, 5-chloro-2-[(1-ethyl-1-methylpropyl)thio]-6-[4-(2-hydroxyethyl)piperazin-1-yl]-1H-benzimidazole, which is structurally distinct from conventional non-peptide antagonists known to date.
Graphical abstractA structurally novel ORL1 selective antagonist with a (piperazin-1-yl)benzimidazole scaffold was identified. Among them, an analogue 28 exhibited sub-nanomolar antagonistic activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Osamu Okamoto, Kensuke Kobayashi, Hiroshi Kawamoto, Satoru Ito, Atsushi Satoh, Tetsuya Kato, Izumi Yamamoto, Sayaka Mizutani, Masaya Hashimoto, Atsushi Shimizu, Hiroki Sakoh, Yasushi Nagatomi, Yoshikazu Iwasawa, Hiroyuki Takahashi, Yasuyuki Ishii,