| Literature DB >> 29259748 |
Masahiko Terakado1, Hidehiro Suzuki1, Kazuya Hashimura1, Motoyuki Tanaka1, Hideyuki Ueda1, Keisuke Hirai1, Masaki Asada1, Masahiro Ikura1, Naoki Matsunaga1, Hiroshi Saga1, Koji Shinozaki1, Naoko Karakawa1, Yuka Takada1, Masashi Minami1, Hiromu Egashira1, Yoshihiro Sugiura1, Masanori Yamada1, Shinji Nakade1, Yoshikazu Takaoka1.
Abstract
Scaffold hopping from the amide group of lead compound ONO-7300243 (1) to a secondary alcohol successfully gave a novel chemotype lysophosphatidic acid receptor 1 (LPA1) antagonist 4. Wash-out experiments using rat isolated urethra showed that compound 4 possesses a tight binding feature to the LPA1 receptor. Further modification of two phenyl groups of 1 to pyrrole and an indane moiety afforded an optimized compound ONO-0300302 (19). Despite its high i.v. clearance, 19 inhibited significantly an LPA-induced increase of intraurethral pressure (IUP) in rat (3 mg/kg, p.o.) and dog (1 mg/kg, p.o.) over 12 h. Binding experiments with [3H]-ONO-0300302 suggest that the observed long duration action is because of the slow tight binding character of 19.Entities:
Year: 2017 PMID: 29259748 PMCID: PMC5733272 DOI: 10.1021/acsmedchemlett.7b00383
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345