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Volumn 23, Issue 19, 2015, Pages 6497-6509
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Synthesis, antiangiogenesis evaluation and molecular docking studies of 1-aryl-3-[(thieno[3,2-b]pyridin-7-ylthio)phenyl]ureas: Discovery of a new substitution pattern for type II VEGFR-2 Tyr kinase inhibitors
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Author keywords
Antiangiogenesis assays; Enzymatic assays; HUVECs; Molecular docking; Thienopyridinethioether 1,3 diarylureas; VEGFR 2 tyrosine kinase inhibitors; Western blotting
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Indexed keywords
1 (3 FLUOROPHENYL) 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 CHLORO 3 (TRIFLUOROMETHYL)PHENYL) 3 [4 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 CYANOPHENYL) 3 [2 (THIENO[3,2 B]PIRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 CYANOPHENYL) 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 CYANOPHENYL) 3 [4 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 FLUOROPHENYL) 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 METHOXYPHENYL) 3 [2 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 METHOXYPHENYL) 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 (4 METHOXYPHENYL) 3 [4 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 ARYL 3 [(THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA DERIVATIVE;
1 PHENYL 3 [2 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 PHENYL 3 [4 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL] 3 M TOLYLUREA;
1 [3 (TRIFLUOROMETHYL)PHENYL] 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 [3 (TRIFLUOROMETHYL)PHENYL] 3 [4 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
1 [4 CHLORO 3 (TRIFLUOROMETHYL)PHENYL] 3 [3 (THIENO[3,2 B]PYRIDIN 7 YLTHIO)PHENYL]UREA;
PROTEIN TYROSINE KINASE INHIBITOR;
SORAFENIB;
UNCLASSIFIED DRUG;
ANGIOGENESIS INHIBITOR;
UREA;
VASCULOTROPIN RECEPTOR 2;
ANTIANGIOGENIC ACTIVITY;
APOPTOSIS;
ARTICLE;
BRDU ASSAY;
CELL MIGRATION;
CELL MIGRATION ASSAY;
CELL PROLIFERATION;
CELL VIABILITY;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG EFFECT;
DRUG POTENCY;
DRUG SYNTHESIS;
ENZYMATIC ASSAY;
ENZYME INHIBITION;
ENZYME PHOSPHORYLATION;
HUMAN;
HUMAN CELL;
IC50;
IMMUNOHISTOCHEMISTRY;
MOLECULAR DOCKING;
PROTEIN EXPRESSION;
STRUCTURE ACTIVITY RELATION;
TUNEL ASSAY;
UMBILICAL VEIN ENDOTHELIAL CELL;
WESTERN BLOTTING;
WOUND HEALING ASSAY;
ANALOGS AND DERIVATIVES;
ANGIOGENESIS;
ANTAGONISTS AND INHIBITORS;
BINDING SITE;
CELL MOTION;
DRUG EFFECTS;
METABOLISM;
PROTEIN TERTIARY STRUCTURE;
SYNTHESIS;
ANGIOGENESIS INHIBITORS;
APOPTOSIS;
BINDING SITES;
CELL MOVEMENT;
CELL PROLIFERATION;
HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS;
HUMANS;
MOLECULAR DOCKING SIMULATION;
NEOVASCULARIZATION, PHYSIOLOGIC;
PROTEIN STRUCTURE, TERTIARY;
STRUCTURE-ACTIVITY RELATIONSHIP;
UREA;
VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR-2;
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EID: 84942191894
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2015.08.010 Document Type: Article |
Times cited : (118)
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References (28)
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