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Volumn 57, Issue , 2012, Pages 74-84
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Synthesis and biological evaluation of 2-benzylamino-4(5)-(6-methylpyridin- 2-yl)-5(4)-([1,2,4]triazolo[1,5-a]-pyridin-6-yl)thiazoles as transforming growth factor-β type 1 receptor kinase inhibitors
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Author keywords
ALK5 inhibitor; Cancer; Cell based luciferase reporter assay; Docking; Fibrosis; Kinase assay; TGF
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Indexed keywords
2 BENZYLAMINO 4(5) (6 METHYLPYRIDIN 2 YL) 5(4) (1,2,4 TRIAZOLO[1,5 A]PYRIDIN 6 YL)THIAZOLE DERIVATIVE;
BROMINE;
DRUG METABOLITE;
IN 1130;
LUCIFERASE;
MITOGEN ACTIVATED PROTEIN KINASE 14;
N (3 FLUOROBENZYL) 4 (6 METHYLPYRIDIN 2 YL) 5 (1,2,4 TRIAZOLO[1,5 A]PYRIDIN 6 YL)THIAZOL 2 AMINE;
NITROGEN;
PROTEIN SERINE THREONINE KINASE INHIBITOR;
SB 505124;
SB 505154;
SMAD2 PROTEIN;
TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1;
TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1 KINASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG BINDING SITE;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME ASSAY;
ENZYME INHIBITION;
ENZYME INHIBITOR INTERACTION;
ENZYME PHOSPHORYLATION;
HUMAN;
HYDROGEN BOND;
IC 50;
IMMUNOBLOTTING;
MOUSE;
NONHUMAN;
OXIDATION;
PROTEIN PHOSPHORYLATION;
STRUCTURE ACTIVITY RELATION;
CELL LINE, TRANSFORMED;
ENZYME ASSAYS;
GENES, REPORTER;
HUMANS;
KERATINOCYTES;
LUCIFERASES;
MOLECULAR DOCKING SIMULATION;
PHOSPHORYLATION;
PROTEIN KINASE INHIBITORS;
PROTEIN-SERINE-THREONINE KINASES;
RECEPTORS, TRANSFORMING GROWTH FACTOR BETA;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIAZOLES;
TRANSFECTION;
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EID: 84867021810
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2012.09.011 Document Type: Article |
Times cited : (20)
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References (26)
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