|
Volumn 45, Issue 18, 2002, Pages 3865-3877
|
Anilinoquinazoline inhibitors of fructose 1,6-bisphosphatase bind at a novel allosteric site: Synthesis, in vitro characterization, and x-ray crystallography
|
Author keywords
[No Author keywords available]
|
Indexed keywords
(2 CHLOROMETHYL 6,7 DIETHOXYQUINAZOLIN 4 YL)[3 (2 METHYLTHIAZOL 4 YL)PHENYL]AMINE;
(2 DIMETHYLAMINOMETHYL 6,7 DIETHOXYQUINAZOLIN 4 YL)[3 (2 METHYLTHIAZOL 4 YL)PHENYL]AMINE;
(6 ETHOXY 7 ISOPROPOXYQUINAZOLIN 4 YL)[3 (2 METHYLTHIAZOL 4 YL)PHENYL]AMINE;
(6,7 DIETHOXYQUINAZOLIN 4 YL)(3 PYRIDIN 3 YLPHENYL)AMINE;
(6,7 DIETHOXYQUINAZOLIN 4 YL)[3 (2 PHENYLTHIAZOL 4 YL)PHENYL]AMINE;
(6,7 DIETHOXYQUINAZOLIN 4 YL)[4 FLUORO 3 (2 METHYLTHIAZOL 4 YL)PHENYL]AMINE;
2 [3 (6,7 DIETHOXYQUINAZOLIN 4 YLAMINO)PHENYL]THIAZOLE 4 CARBOXYLAMIDE;
4 [3 (6,7 DIETHOXYQUINAZOLIN 4 YLAMINO)PHENYL]THIAZOLE 2 CARBOXYLAMIDE;
ANTIDIABETIC AGENT;
EPIDERMAL GROWTH FACTOR RECEPTOR KINASE;
FRUCTOSE BISPHOSPHATASE;
FRUCTOSE BISPHOSPHATASE INHIBITOR;
QUINAZOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ALLOSTERISM;
ARTICLE;
CHEMICAL MODIFICATION;
DRUG BINDING;
DRUG BINDING SITE;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVE SITE;
ENZYME BINDING;
ENZYME INHIBITION;
ENZYME SUBUNIT;
MOLECULAR RECOGNITION;
SITE DIRECTED MUTAGENESIS;
STRUCTURE ACTIVITY RELATION;
STRUCTURE ANALYSIS;
X RAY CRYSTALLOGRAPHY;
ALLOSTERIC SITE;
ANILINE COMPOUNDS;
ANIMALS;
CATALYTIC DOMAIN;
CRYSTALLOGRAPHY, X-RAY;
ENZYME INHIBITORS;
FRUCTOSE-BISPHOSPHATASE;
HUMANS;
MODELS, MOLECULAR;
MUTAGENESIS, SITE-DIRECTED;
QUINAZOLINES;
RABBITS;
RATS;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
|
EID: 0037194657
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm010496a Document Type: Article |
Times cited : (88)
|
References (62)
|