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Volumn 53, Issue , 2012, Pages 356-363
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Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry
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Author keywords
Anti cancer activity; Benzopyran 4 one derivative; Bioisosteric transformation; Click chemistry; Synthesis
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Indexed keywords
3 [[4 [(4 OXO 4H CHROMEN 7 YLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]BENZONITRILE;
4 [[4 [(4 OXO 4H CHROMEN 7 YLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]BENZONITRILE;
7 [(1 BENZYL 1H 1,2,3 TRIAZOL 4 YL)METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (2 BROMOBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (2 CHLOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (2 FLUOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOX] 4H CHROMEN 4 ONE;
7 [[1 (2 METHYLBENZYL) 1H 1,2,3 TRIAZOL 4 YL)METHOXY) 4H CHROMEN 4 ONE;
7 [[1 (2,4 DICHLOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (3 BROMOBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (3 CHLOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (3 FLUOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (3 NITROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 BROMOBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 CHLOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 FLUOROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 METHOXYBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 METHYLBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 NITROBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1 (4 TERT BUTYLBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
7 [[1(3 METHYLBENZYL) 1H 1,2,3 TRIAZOL 4 YL]METHOXY] 4H CHROMEN 4 ONE;
ANTINEOPLASTIC AGENT;
BENZOPYRAN DERIVATIVE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
APOPTOSIS;
ARTICLE;
CONTROLLED STUDY;
CYTOTOXICITY TEST;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IC 50;
ANTINEOPLASTIC AGENTS;
APOPTOSIS;
CELL LINE, TUMOR;
CHEMISTRY TECHNIQUES, SYNTHETIC;
CLICK CHEMISTRY;
COUMARINS;
HUMANS;
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EID: 84861595329
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2012.04.026 Document Type: Article |
Times cited : (31)
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References (30)
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