哌啶
砜
基质金属蛋白酶
体内
化学
医学
关节炎
内科学
药理学
立体化学
生物化学
生物
生物技术
高分子化学
作者
Daniel P. Becker,Thomas E. Barta,Louis J. Bedell,Terri L. Boehm,Brian R. Bond,Jeffery N. Carroll,Chris P. Carron,Gary DeCrescenzo,Alan M. Easton,John N. Freskos,Chris L. Funckes-Shippy,Marcia I. Heron,Susan L. Hockerman,Carol Pearcy Howard,James R. Kiefer,Madeleine H. Li,Karl J. Mathis,Joseph J. McDonald,Pramod P. Mehta,Grace E. Munie
摘要
α-Sulfone-α-piperidine and α-tetrahydropyranyl hydroxamates were explored that are potent inhibitors of MMP's-2, -9, and -13 that spare MMP-1, with oral efficacy in inhibiting tumor growth in mice and left-ventricular hypertrophy in rats and in the bovine cartilage degradation ex vivo explant system. α-Piperidine 19v (SC-78080/SD-2590) was selected for development toward the initial indication of cancer, while α-piperidine and α-tetrahydropyranyl hydroxamates 19w (SC-77964) and 9i (SC-77774), respectively, were identified as backup compounds.
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