Recent advances in matrix metalloproteinase inhibitor research

被引:266
作者
Beckett, RP
Davidson, AH
Drummond, AH
Huxley, P
Whittaker, M
机构
[1] British Biotech Pharmaceuticals Ltd, Oxford, OX4 5LY, Watlington Road
关键词
D O I
10.1016/1359-6446(96)89115-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The matrix metalloprolteinases (MMPs) are a family of zinc-dependent enzymes that degrade all of the major components of the extracellular matrix. Over-expression and activation of MMPs have been linked with a range of diseases for which good therapeutic approaches are currently sought, such as arthritis, cancer and multiple sclerosis. Inhibition of MMPs has therefore become the focus of considerable interest, and potential therapeutic applications continue to grow. Orally active, broad-spectrum inhibitors have been identified, and some of these are undergoing clinical evaluation. Structural information on MMP-inhibitor complexes is now available, enabling the structure-based design of selective MMP inhibitors.
引用
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页码:16 / 26
页数:11
相关论文
共 87 条
[1]   MATRIX METALLOPROTEINASE-2 IS AN INTERSTITIAL COLLAGENASE - INHIBITOR-FREE ENZYME CATALYZES THE CLEAVAGE OF COLLAGEN FIBRILS AND SOLUBLE NATIVE TYPE-I COLLAGEN GENERATING THE SPECIFIC 3/4-LENGTH AND 1/4-LENGTH FRAGMENTS [J].
AIMES, RT ;
QUIGLEY, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5872-5876
[2]  
[Anonymous], [No title captured]
[3]  
[Anonymous], 2003, Drugs R&D, V4, P198, Patent No. 9402447
[4]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[5]  
BEATTIE GJ, 1994, 8 NCI EORTC S NEW DR
[6]  
BECKETT RP, 1995, Patent No. 95119956
[7]  
BEELEY NRA, 1995, Patent No. 9504033
[8]   SYNTHESIS OF NOVEL MODIFIED DIPEPTIDE INHIBITORS OF HUMAN COLLAGENASE - BETA-MERCAPTO CARBOXYLIC-ACID DERIVATIVES [J].
BESZANT, B ;
BIRD, J ;
GASTER, LM ;
HARPER, GP ;
HUGHES, I ;
KARRAN, EH ;
MARKWELL, RE ;
MILESWILLIAMS, AJ ;
SMITH, SA .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (25) :4030-4039
[9]   THE X-RAY CRYSTAL-STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN NEUTROPHIL COLLAGENASE INHIBITED BY A SUBSTRATE-ANALOG REVEALS THE ESSENTIALS FOR CATALYSIS AND SPECIFICITY [J].
BODE, W ;
REINEMER, P ;
HUBER, R ;
KLEINE, T ;
SCHNIERER, S ;
TSCHESCHE, H .
EMBO JOURNAL, 1994, 13 (06) :1263-1269
[10]   INHIBITION OF COLLAGENASE BY ARANCIAMYCIN AND ARANCIAMYCIN DERIVATIVES [J].
BOLS, M ;
BINDERUP, L ;
HANSEN, J ;
RASMUSSEN, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (15) :2768-2771