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Volumn 21, Issue 5, 2011, Pages 1480-1483
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Scaffold oriented synthesis. Part 4: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing heterocycle forming and multicomponent reactions
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Author keywords
Egfr inhibitors; Gsk3 inhibitors; Imidazopyridines; Imidazopyrimidine; Kinase inhibitors; Kinase scaffolds; MCR; multicomponent reactions; Rock2 inhibitors; Van Leusen reactions
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Indexed keywords
AURORA B KINASE;
AURORA KINASE INHIBITOR;
EPIDERMAL GROWTH FACTOR RECEPTOR;
EPIDERMAL GROWTH FACTOR RECEPTOR KINASE INHIBITOR;
GLYCOGEN SYNTHASE KINASE 3 INHIBITOR;
GLYCOGEN SYNTHASE KINASE 3BETA;
IMIDAZOLE DERIVATIVE;
INDAZOLE DERIVATIVE;
P21 ACTIVATED KINASE 4;
PHOSPHOTRANSFERASE INHIBITOR;
PROTEIN KINASE PIM 1;
PYRIMIDINE DERIVATIVE;
RHO KINASE;
RHO KINASE 2;
RHO KINASE INHIBITOR;
THIAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
VASCULOTROPIN INHIBITOR;
VASCULOTROPIN RECEPTOR 2;
ARTICLE;
DRUG DESIGN;
DRUG POTENCY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ENZYME ASSAY;
SUBSTITUTION REACTION;
DRUG DESIGN;
HETEROCYCLIC COMPOUNDS;
INDAZOLES;
MOLECULAR STRUCTURE;
PROTEIN KINASE INHIBITORS;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 79951723545
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2011.01.001 Document Type: Article |
Times cited : (41)
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References (12)
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