化学
铅化合物
趋化性
固相合成
受体
化学合成
立体化学
组合化学
体外
生物化学
肽
作者
Wilna J. Moree,Kenichiro Kataoka,Michele M. Ramirez-Weinhouse,Tatsuki Shiota,Minoru Imai,Takaharu Tsutsumi,Masaki Sudo,Noriaki Endo,Yumiko Muroga,Takahiko Hada,Dewey Fanning,John B. Saunders,Yoshinori Kato,Peter Myers,Christine M. Tarby
标识
DOI:10.1016/j.bmcl.2008.02.015
摘要
SAR studies were conducted around lead compound 1 using high-throughput parallel solution and solid phase synthesis. Our lead optimization efforts led to the identification of several CCR2b antagonists with potent activity in both binding and functional assays [Compound 71 CCR2b Binding IC(50) 3.2 nM; MCP-1-Induced Chemotaxis IC(50) 0.83 nM; Ca(2+) Flux IC(50) 7.5 nM].
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