Comparative QSAR study of tyrosine kinase inhibitors

被引:45
作者
Kurup, A [1 ]
Garg, R [1 ]
Hansch, C [1 ]
机构
[1] Pomona Coll, Dept Chem, Claremont, CA 91711 USA
关键词
D O I
10.1021/cr010154c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A comparative QSAR study of tyrosine kinase inhibitors was presented. The results and discussions were presented for inhibitors of epidermal growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR), fibroblast growth factor receptor (FGFR) and vascular endothelial growth factor receptor (VEGF-R2) tyrosine kinase. The inhibitory activity of the compounds was expressed in molar concentration.
引用
收藏
页码:2573 / 2600
页数:28
相关论文
共 113 条
[61]   TYROSINE KINASE INHIBITION - AN APPROACH TO DRUG DEVELOPMENT [J].
LEVITZKI, A ;
GAZIT, A .
SCIENCE, 1995, 267 (5205) :1782-1788
[62]   TYRPHOSTINS AS MOLECULAR TOOLS AND POTENTIAL ANTIPROLIFERATIVE DRUGS [J].
LEVITZKI, A ;
GILON, C .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1991, 12 (05) :171-174
[63]  
Levitzki A, 1996, ANTI-CANCER DRUG DES, V11, P175
[64]  
LODISH H, 2000, MOL CELL BIOL, P849
[65]  
LODISH H, 2000, MOL CELL BIOL, P1054
[66]   GLIAL GROWTH-FACTORS ARE ALTERNATIVELY SPLICED ERBB2 LIGANDS EXPRESSED IN THE NERVOUS-SYSTEM [J].
MARCHIONNI, MA ;
GOODEARL, ADJ ;
CHEN, MS ;
BERMINGHAMMCDONOGH, O ;
KIRK, C ;
HENDRICKS, M ;
DANEHY, F ;
MISUMI, D ;
SUDHALTER, J ;
KOBAYASHI, K ;
WROBLEWSKI, D ;
LYNCH, C ;
BALDASSARE, M ;
HILES, I ;
DAVIS, JB ;
HSUAN, JJ ;
TOTTY, NF ;
OTSU, M ;
MCBURNEY, RN ;
WATERFIELD, MD ;
STROOBANT, P ;
GWYNNE, D .
NATURE, 1993, 362 (6418) :312-318
[67]   EXPRESSION OF PP60C-SRC IN HUMAN SMALL-CELL AND NON-SMALL-CELL LUNG CARCINOMAS [J].
MAZURENKO, NN ;
KOGAN, EA ;
ZBOROVSKAYA, IB ;
KISSELJOV, FL .
EUROPEAN JOURNAL OF CANCER, 1992, 28A (2-3) :372-377
[68]   ON NATURE OF ALLOSTERIC TRANSITIONS - A PLAUSIBLE MODEL [J].
MONOD, J ;
WYMAN, J ;
CHANGEUX, JP .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 12 (01) :88-&
[69]  
MORISHIGE KI, 1991, CANCER RES, V51, P5322
[70]  
MOSCATELLO DK, 1995, CANCER RES, V55, P5536