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Volumn 20, Issue 21, 2012, Pages 6356-6365
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Design, synthesis and biological evaluation of heterocyclic azoles derivatives containing pyrazine moiety as potential telomerase inhibitors
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Author keywords
Anti tumor activity; Molecular docking; Oxadiazole; Pyrazine; Telomerase; Thiadiazole; Triazole
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Indexed keywords
2 (BENZYLTHIO) 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 (BENZYLTHIO) 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(2 BROMOBENZYL)OXY] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2 BROMOBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2 BROMOBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(2 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(2 FLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2 FLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(2,4 DIFLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2,4 DIFLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(2,6 DIFLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(2,6 DIFLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(3 BROMOBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(3 BROMOBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(3 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(3 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(4 BROMOBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(4 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(4 CHLOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [(4 FLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 OXADIAZOLE;
2 [(4 FLUOROBENZYL)THIO] 5 (PYRAZIN 2 YL) 1,3,4 THIADIAZOLE;
2 [5 [(2 BROMOBENZYL)THIO] 4 PHENYL 4H 1,2,4 TRIAZOL 3 YL]PYRAZINE;
2 [5 [(2 CHLOROBENZYL)THIO] 4 PHENYL 4H 1,2,4 TRIAZOL 3 YL]PYRAZINE;
2 [5 [(2 FLUOROBENZYL)THIO] 4 PHENYL 4H 1,2,4 TRIAZOL 3 YL]PYRAZINE;
2 [5 [(3 CHLOROBENZYL)THIO] 4 PHENYL 4H 1,2,4 TRIAZOL 3 YL]PYRAZINE;
PYRROLE DERIVATIVE;
TELOMERASE;
TELOMERASE INHIBITOR;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ANTINEOPLASTIC ACTIVITY;
ANTIPROLIFERATIVE ACTIVITY;
APOPTOSIS;
ARTICLE;
CANCER CELL CULTURE;
CANCER INHIBITION;
CELL STRAIN HEPG2;
CELL STRAIN SW1116;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
IC 50;
MOLECULAR DOCKING;
ANTINEOPLASTIC AGENTS;
APOPTOSIS;
AZOLES;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
DRUG SCREENING ASSAYS, ANTITUMOR;
ENZYME INHIBITORS;
HEP G2 CELLS;
HETEROCYCLIC COMPOUNDS;
HUMANS;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
PYRAZINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
TELOMERASE;
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EID: 84867571377
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2012.08.059 Document Type: Article |
Times cited : (46)
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References (31)
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