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Volumn 16, Issue 18, 2008, Pages 8685-8696
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Synthesis, biological active molecular design, and molecular docking study of novel deazaflavin-cholestane hybrid compounds
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Author keywords
5 Deazaflavin; Cholestane; Hybrid compound; LigandFit; Protein tyrosine kinase
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Indexed keywords
2 HYDROXYMETHYLENECHOLEST 4 EN 3 ONE;
5 DEAZAFLAVIN;
8' ETHYL 3' METHYL 5' DEAZACHOLEST 2,4 DIENO[2,3 G]PTERIDINE 2',4'(3'H,8'H) DIONE;
CHOLESTANE DERIVATIVE;
DIPHENYL ETHER;
PROTEIN TYROSINE KINASE;
PTERIDINE DERIVATIVE;
PYRIMIDINE DERIVATIVE;
STEROID;
TOLUENESULFONIC ACID DERIVATIVE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BINDING AFFINITY;
CANCER CELL CULTURE;
CONTROLLED STUDY;
DRUG BINDING SITE;
DRUG CYTOTOXICITY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
HYBRID;
IN VITRO STUDY;
POLYMERIZATION;
STRUCTURE ACTIVITY RELATION;
ALGORITHMS;
BINDING SITES;
CELL LINE, TUMOR;
CHOLESTANES;
DRUG DESIGN;
FLAVINS;
HUMANS;
INHIBITORY CONCENTRATION 50;
KB CELLS;
LEUKEMIA, LYMPHOID;
LIGANDS;
MODELS, MOLECULAR;
PROTEIN-TYROSINE KINASES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 51449118185
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2008.07.089 Document Type: Article |
Times cited : (19)
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References (36)
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