Sulfonylated aminothiazoles as new small molecule inhibitors of protein phosphatases
作者:Peter Wipf、Diana C. Aslan、Eileen C. Southwick、John S. Lazo
DOI:10.1016/s0960-894x(00)00658-2
日期:2001.2
Based on a previously identified lead structure, SC-alpha alpha delta9, we have developed a versatile new chemical scaffold that can be readily modified to generate libraries of both Tyr and dual specificity phosphatase inhibitors with reduced molecular weight and lipophilicity. The most potent analogue identified to dare, aminothiazole 8z, inhibits the dual specificity phosphatase Cdc25B with a K-i of 4.6 +/- 0.4 muM and a Hill coefficient of 2. (C) 2001 Elsevier Science Ltd. Ail rights reserved.
[EN] ANALOGUES OF ANTI-FIBROTIC AGENTS<br/>[FR] ANALOGUES D'AGENTS ANTIFIBROTIQUES
申请人:FIBROTECH THERAPEUTICS PTY LTD
公开号:WO2010144959A1
公开(公告)日:2010-12-23
The present invention relates to analogues of anti-fibrotic agents having the formula (I) with the substituents as described within the specification. The present invention also relates to methods for their preparation.