Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors

被引:460
作者
Liao, Jeffrey Jie-Lou
机构
[1] TransTech Pharma, High Point, NC 27265 USA
[2] Duke Univ, Dept Chem, Durham, NC 27708 USA
关键词
GROWTH-FACTOR RECEPTOR; CYCLIN-DEPENDENT KINASE; STRUCTURE-GUIDED DESIGN; ABL TYROSINE KINASE; STRUCTURAL BASIS; CRYSTAL-STRUCTURE; ANTITUMOR-ACTIVITY; DRUG DISCOVERY; AURORA KINASE; MAP KINASE;
D O I
10.1021/jm0608107
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
[No abstract available]
引用
收藏
页码:409 / 424
页数:16
相关论文
共 133 条
[21]   Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases [J].
Carter, TA ;
Wodicka, LM ;
Shah, NP ;
Velasco, AM ;
Fabian, MA ;
Treiber, DK ;
Milanov, ZV ;
Atteridge, CE ;
Biggs, WH ;
Edeen, PT ;
Floyd, M ;
Ford, JM ;
Grotzfeld, RM ;
Herrgard, S ;
Insko, DE ;
Mehta, SA ;
Patel, HK ;
Pao, W ;
Sawyers, CL ;
Varmus, H ;
Zarrinkar, PP ;
Lockhart, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (31) :11011-11016
[22]   Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors [J].
Chang, YT ;
Gray, NS ;
Rosania, GR ;
Sutherlin, DP ;
Kwon, S ;
Norman, TC ;
Sarohia, R ;
Leost, M ;
Meijer, L ;
Schultz, PG .
CHEMISTRY & BIOLOGY, 1999, 6 (06) :361-375
[23]   Recent kinase and kinase inhibitor X-ray structures: Mechanisms of inhibition and selectivity insights [J].
Cherry, M ;
Williams, DH .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (06) :663-673
[24]   Molecular design and bioavailability [J].
Clark, RD ;
Wolohan, PRN .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2003, 3 (11) :1269-1288
[25]   United States Food and Drug Administration drug approval summary: Gefitinib (ZD1839; Iressa) tablets [J].
Cohen, MH ;
Williams, GA ;
Sridhara, R ;
Chen, G ;
McGuinn, WD ;
Morse, D ;
Abraham, S ;
Rahman, A ;
Liang, CY ;
Lostritto, R ;
Baird, A ;
Pazdur, R .
CLINICAL CANCER RESEARCH, 2004, 10 (04) :1212-1218
[26]   Structural bioinformatics-based design of selective, irreversible kinase inhibitors [J].
Cohen, MS ;
Zhang, C ;
Shokat, KM ;
Taunton, J .
SCIENCE, 2005, 308 (5726) :1318-1321
[27]   Protein kinases - the major drug targets of the twenty-first century? [J].
Cohen, P .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (04) :309-315
[28]   Structural basis of Src tyrosine kinase inhibition with a new class of potent and selective trisubstituted purine-based compounds [J].
Dalgarno, D ;
Stehle, T ;
Narula, S ;
Schelling, P ;
van Schravendijk, MR ;
Adams, S ;
Andrade, L ;
Keats, J ;
Ram, M ;
Jin, L ;
Grossman, T ;
MacNeil, I ;
Metcalf, C ;
Shakespeare, W ;
Wang, Y ;
Keenan, T ;
Sundaramoorthi, R ;
Bohacek, R ;
Weigele, M ;
Sawyer, T .
CHEMICAL BIOLOGY & DRUG DESIGN, 2006, 67 (01) :46-57
[29]   Issues and progress with protein kinase inhibitors for cancer treatment [J].
Dancey, J ;
Sausville, EA .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (04) :296-313
[30]   Specificity and mechanism of action of some commonly used protein kinase inhibitors [J].
Davies, SP ;
Reddy, H ;
Caivano, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2000, 351 (351) :95-105