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
[51]   Discovery and evaluation of 2-anilino-5-aryloxazoles as a novel class of VEGFR2 kinase inhibitors [J].
Harris, PA ;
Cheung, M ;
Hunter, RN ;
Brown, ML ;
Veal, JM ;
Nolte, RT ;
Wang, LP ;
Liu, W ;
Crosby, RM ;
Johnson, JH ;
Epperly, AH ;
Kumar, R ;
Luttrell, DK ;
Stafford, JA .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (05) :1610-1619
[52]   SAR and inhibitor complex structure determination of a novel class of potent and specific Aurora kinase inhibitors [J].
Heron, NM ;
Anderson, M ;
Blowers, DP ;
Breed, J ;
Eden, JM ;
Green, S ;
Hill, GB ;
Johnson, T ;
Jung, FH ;
McMiken, HHJ ;
Mortlock, AA ;
Pannifer, AD ;
Pauptit, RA ;
Pink, J ;
Roberts, NJ ;
Rowsell, S .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (05) :1320-1323
[53]  
HIROSHI H, 2005, CURR TOP MED CHEM, V5, P167
[54]   CRYSTAL-STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HUMAN INSULIN-RECEPTOR [J].
HUBBARD, SR ;
WEI, L ;
ELIS, L ;
HENDRICKSON, WA .
NATURE, 1994, 372 (6508) :746-754
[55]   The conformational plasticity of protein kinases [J].
Huse, M ;
Kuriyan, J .
CELL, 2002, 109 (03) :275-282
[56]   The structure of dimeric ROCK I reveals the mechanism for ligand selectivity [J].
Jacobs, M ;
Hayakawa, K ;
Swenson, L ;
Bellon, S ;
Fleming, M ;
Taslimi, P ;
Doran, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (01) :260-268
[57]   Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002 [J].
Jacobs, MD ;
Black, J ;
Futer, O ;
Swenson, L ;
Hare, B ;
Fleming, M ;
Saxena, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :13728-13734
[58]   From the insoluble dye indirubin towards highly active, soluble CDK2-inhibitors [J].
Jautelat, R ;
Brumby, T ;
Schäfer, M ;
Briem, H ;
Eisenbrand, G ;
Schwahn, S ;
Krüger, M ;
Lücking, U ;
Prien, O ;
Siemeister, G .
CHEMBIOCHEM, 2005, 6 (03) :531-540
[59]   Discovery of novel and potent thiazoloquinazolines as selective Aurora A and B kinase inhibitors [J].
Jung, FH ;
Pasquet, G ;
Lambert-van der Brempt, C ;
Lohmann, JJM ;
Warin, N ;
Renaud, F ;
Germain, H ;
De Savi, C ;
Roberts, N ;
Johnson, T ;
Dousson, C ;
Hill, GB ;
Mortlock, AA ;
Heron, N ;
Wilkinson, RW ;
Wedge, SR ;
Heaton, SP ;
Odedra, R ;
Keen, NJ ;
Green, S ;
Brown, E ;
Thompson, K ;
Brightwell, S .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (03) :955-970
[60]   Signal transduction therapy with rationally designed kinase inhibitors [J].
Keri, Gyoergy ;
Orfi, Laszlo ;
Eros, Daniel ;
Hegymegi-Barakonyi, Balint ;
Szantai-Kis, Csaba ;
Horvath, Zoltan ;
Waczek, Frigyes ;
Marosfalvi, Jeno ;
Szabadkai, Istvan ;
Pato, Janos ;
Greff, Zoltan ;
Hafenbradl, Doris ;
Daub, Henrik ;
Mueller, Gerhard ;
Klebl, Bert ;
Ullrich, Axel .
CURRENT SIGNAL TRANSDUCTION THERAPY, 2006, 1 (01) :67-95