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Volumn 19, Issue 23, 2009, Pages 6637-6639
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Synthesis of 3β, 7α, 11α-trihydroxy-pregn-21-benzylidene-5-en-20-one derivatives and their cytotoxic activities
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Author keywords
Biotransformation; Claisen Schimidt condensation; Cytotoxicity; Hydroxylation; Mucor circinelloides lusitanicus; Pregnenolone
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Indexed keywords
3BETA,7ALPHA,11ALPHA TRIHYDROXY PREGN 21 BENZYLIDENE 5 EN 20 ONE DERIVATIVE;
ANTINEOPLASTIC AGENT;
MAGNESIUM;
ORIDONIN;
PREGNENOLONE;
UNCLASSIFIED DRUG;
DRUG DERIVATIVE;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER INHIBITION;
CARBON NUCLEAR MAGNETIC RESONANCE;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG EFFICACY;
DRUG SYNTHESIS;
DRUG TRANSFORMATION;
FERMENTATION;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
MUCOR;
MUCOR CIRCINELLOIDES LUSITANICUS;
PH;
PROTON NUCLEAR MAGNETIC RESONANCE;
X RAY CRYSTALLOGRAPHY;
CELL PROLIFERATION;
CHEMICAL STRUCTURE;
CHEMISTRY;
DRUG EFFECT;
DRUG SCREENING;
METABOLISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TUMOR CELL LINE;
MUCOR CIRCINELLOIDES;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
CRYSTALLOGRAPHY, X-RAY;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
MUCOR;
PREGNENOLONE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 71749089264
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2009.10.019 Document Type: Article |
Times cited : (43)
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References (30)
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