发明名称 METALLOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR PHARMACEUTICAL USES, AND METHODS AND INTERMEDIATES USEFUL FOR THEIR PREPARATION.
摘要 The invention relates to compounds of formula (1) wherein: Z is O or S; V is a divalent radical which together with C* and N forms a ring having six ring atoms, where each of said ring atoms other than C* and N independently is unsubstituted or substituted by a suitable substituent, and at least one of said other ring atoms is a heteroatom selected from O, N and S, and the remainder is carbon atoms; and Ar is an aryl or heteroaryl group; and pharmaceutically acceptable prodrugs, salts and solvates thereof. The invention further relates to pharmaceutically acceptable prodrugs, salts and solvates of these compounds. The invention also relates to methods of inhibiting the activity of metalloproteinases by administering a compound of formula (1) or a prodrug, salt or solvate thereof. The invention further relates to pharmaceutical compositions comprising an effective amount of these compounds, prodrugs, salts, and solvates. The invention still further relates to methods and intermediates useful for preparing these compounds, prodrugs, salts, and solvates.
申请公布号 MX9804457(A) 申请公布日期 1998.09.30
申请号 MX19980004457 申请日期 1998.06.04
申请人 AGOURON PHARMACEUTICALS, INC. 发明人 SCOTT E. ZOOK;RAYMOND DAGNINO, JR.;MICHAEL E. DEASON;STEVEN L. BENDER;MICHAEL J. MELNICK
分类号 C07D241/04;A61K31/00;A61K31/44;A61K31/4409;A61K31/4427;A61K31/495;A61K31/50;A61K31/535;A61K31/5375;A61K31/54;A61K31/541;A61P19/02;A61P29/00;A61P35/00;A61P35/04;A61P43/00;C07C309/28;C07D;C07D213/62;C07D213/68;C07D213/70;C07D213/89;C07D233/54;C07D233/64;C07D239/04;C07D249/08;C07D265/30;C07D277/62;C07D279/00;C07D279/12;C07D295/00;C07D307/38;C07D401/00;C07D401/12;C07D403/12;C07D413/00;C07D413/12;C07D417/00;C07D417/12;C07F7/18 主分类号 C07D241/04
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