化学
异羟肟酸
酶
生物利用度
效力
选择性
酶抑制剂
立体化学
化学合成
肿瘤坏死因子α
结构-活动关系
药理学
生物化学
体外
内分泌学
催化作用
医学
作者
Gregory R. Ott,Naoyuki Asakawa,Zhonghui Lu,Rui‐Qin Liu,Maryanne Covington,Krishna Vaddi,Mingxin Qian,Robert Newton,David D. Christ,James M. Traskos,Carl P. Decicco,James J.‐W. Duan
标识
DOI:10.1016/j.bmcl.2007.11.059
摘要
Selective inhibitors of TNF-α Converting Enzyme (TACE) based on (1R,2S)-cyclopentyl, (3S,4S)-pyrrolidinyl, and (3R,4S)-tetrahydrofuranyl β-benzamido hydroxamic acids have been synthesized and evaluated. This study has led to the discovery of novel inhibitors whose profiles include activity against TACE in an enzyme assay, potency in the suppression of LPS-stimulated TNF-α in human whole blood, selectivity against a panel of MMPs and oral bioavailability.
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