Structural biology in drug design: selective protein kinase inhibitors

被引:94
作者
Scapin, G [1 ]
机构
[1] Merck Res Labs, Rahway, NJ 07065 USA
关键词
D O I
10.1016/S1359-6446(02)02290-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein kinases have a fundamental role in signal transduction pathways, and aberrant kinase activity has been observed in many diseases. In recent years, kinase inhibition has become a major area for therapeutic intervention and a variety of kinase inhibitor pharmacophores has been described. This review illustrates some of the efforts and results in the field of structure-based design of protein kinase inhibitors. The methods and results discussed here illustrate the power of structure-based design in lead discovery, for example via virtual screening and in guiding the optimization of the pharmacological properties of these molecules.
引用
收藏
页码:601 / 611
页数:11
相关论文
共 74 条
[1]   Kinetic and catalytic mechanisms of protein kinases [J].
Adams, JA .
CHEMICAL REVIEWS, 2001, 101 (08) :2271-2290
[2]  
Adams JL, 2001, PROGR MED CHEM, V38, P1, DOI 10.1016/S0079-6468(08)70091-2
[3]   Substrate competitive inhibitors of IGF-1 receptor kinase [J].
Blum, G ;
Gazit, A ;
Levitzki, A .
BIOCHEMISTRY, 2000, 39 (51) :15705-15712
[4]   Chemical inhibitors of protein kinases [J].
Bridges, AJ .
CHEMICAL REVIEWS, 2001, 101 (08) :2541-2571
[5]  
Broadbridge R. J., 2000, Current Drug Targets, V1, P365, DOI 10.2174/1389450003349074
[6]   The cell cycle and drug discovery: the promise and the hope [J].
Brooks, G ;
La Thangue, NB .
DRUG DISCOVERY TODAY, 1999, 4 (10) :455-464
[7]   Structure-based design and synthesis of a novel class of Src SH2 inhibitors [J].
Buchanan, JL ;
Bohacek, RS ;
Luke, GP ;
Hatada, M ;
Lu, XD ;
Dalgarno, DC ;
Narula, SS ;
Yuan, R ;
Holt, DA .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1999, 9 (16) :2353-2358
[8]  
Burke TR, 2001, BIOPOLYMERS, V60, P32, DOI 10.1002/1097-0282(2001)60:1<32::AID-BIP1002>3.0.CO
[9]  
2-I
[10]   MAP kinases [J].
Chen, Z ;
Gibson, TB ;
Robinson, F ;
Silvestro, L ;
Pearson, G ;
Xu, BE ;
Wright, A ;
Vanderbilt, C ;
Cobb, MH .
CHEMICAL REVIEWS, 2001, 101 (08) :2449-2476