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Volumn 14, Issue 16, 2006, Pages 5643-5650
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Novel benzofuran inhibitors of human mitogen-activated protein kinase phosphatase-1
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Author keywords
Cancer; Enzyme inhibition; Mitogenic signaling; Protein tyrosine phosphatases; Structure activity relationship
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Indexed keywords
2 [2 (5 CARBAMIMIDOYLBENZOFURAN 2 YL)VINYL] 1H INDOLE 6 CARBOXIMIDAMIDE BIS(HYDROGEN CHLORIDE);
2 [2 (5 CYANOBENZOFURAN 2 YL)ETHYL] 1H INDOLE 6 CARBONITRILE;
2 [2 (5 CYANOBENZOFURAN 2 YL)VINYL] 1H INDOLE 6 CARBONITRILE;
2 [2 [5 (4,5 DIHYDRO 1H IMIDAZOL 2 YL)BENZOFURAN 2 YL]VINYL] 6 (1H IMIDAZOL 2 YL) 1H INDOLE;
2 [4 (4 CARBAMIMIDOYLPHENOXY)PHENYL] 1H INDOLE 6 CARBOXIMIDAMIDE BIS(HYDROGEN FORMATE);
2 [[2 (5 METHYLENEAMINOGUANIDYL)BENZOFURAN 2 YL]VINYL] 1H INDOLE 6 METHYLENEAMINOGUANIDINE BIS(DIHYDROGEN CARBONATE);
4 [4 (6 ISOCYANO 1H INDOL 2 YL)PHENOXY]BENZONITRILE;
6 (4,5 DIHYDRO 1H IMIDAZOL 2 YL) 2 [2 [5 (4,5 DIHYDRO 1H IMIDAZOL 2 YL)BENZOFURAN 2 YL]VINYL] 1H INDOL 3 YLAMINE;
BENZOFURAN DERIVATIVE;
ESTERASE INHIBITOR;
METHYL 3 (6 CYANO 1H INDOL 2 YL)ACRYLATE;
MITOGEN ACTIVATED PROTEIN KINASE PHOSPHATASE 1;
NSC 357756;
NU 126;
NU 135;
NU 145;
NU 154;
NU 176;
NU 2 157;
NU 2 168;
PHOSPHATASE;
PHOSPHOPROTEIN PHOSPHATASE;
PROTEIN TYROSINE PHOSPHATASE;
UNCLASSIFIED DRUG;
ARTICLE;
CONTROLLED STUDY;
DRUG SCREENING;
DRUG STRUCTURE;
ENZYME INHIBITION;
HUMAN;
IC 50;
OXIDATION REDUCTION REACTION;
BENZOFURANS;
CDC25 PHOSPHATASE;
CELL CYCLE PROTEINS;
ENZYME ACTIVATION;
ENZYME INHIBITORS;
HUMANS;
IMIDAZOLES;
INHIBITORY CONCENTRATION 50;
KINETICS;
MITOGEN-ACTIVATED PROTEIN KINASE 1;
PHOSPHORYLATION;
PROTEIN-TYROSINE-PHOSPHATASE;
SUBSTRATE SPECIFICITY;
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EID: 33745610883
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2006.04.036 Document Type: Article |
Times cited : (54)
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References (26)
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