Sheppeck James E, Gilmore John L, Tebben Andrew, Xue Chu-Biao, Liu Rui-Qin, Decicco Carl P, Duan James J-W
Bristol-Myers Squibb Pharmaceutical Research Institute, PO Box 4000, Princeton, NJ 08543-4000, USA.
Bioorg Med Chem Lett. 2007 May 15;17(10):2769-74. doi: 10.1016/j.bmcl.2007.02.076. Epub 2007 Mar 3.
We have discovered selective and potent inhibitors of TACE that replace the common hydroxamate zinc binding group with a hydantoin, triazolone, and imidazolone heterocycle. These novel heterocyclic inhibitors of a zinc metalloprotease were designed using a pharmacophore model that we previously described while developing hydantoin and pyrimidinetrione (barbiturate) inhibitors of TACE. The potency and binding orientation of these inhibitors is discussed and they are modeled into the X-ray crystal structure of TACE and compared to hydroxamate and earlier hydantoin TACE inhibitors which share the same 4-[(2-methyl-4-quinolinyl)methoxy]benzoyl P1' group.
我们已经发现了TACE的选择性强效抑制剂,这些抑制剂用乙内酰脲、三唑酮和咪唑酮杂环取代了常见的异羟肟酸锌结合基团。这些新型锌金属蛋白酶杂环抑制剂是使用我们之前在开发TACE的乙内酰脲和嘧啶三酮(巴比妥酸盐)抑制剂时描述的药效团模型设计的。讨论了这些抑制剂的效力和结合方向,并将它们构建到TACE的X射线晶体结构模型中,与具有相同4-[(2-甲基-4-喹啉基)甲氧基]苯甲酰基P1'基团的异羟肟酸和早期乙内酰脲TACE抑制剂进行比较。