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Volumn 54, Issue , 2012, Pages 728-739
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Synthesis and biological evaluation of novel unsaturated carboxysteroids as human 5α-reductase inhibitors: A legitimate approach
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Author keywords
17a Aza steroids; 5 Reductase; Benign prostatic hyperplasia; Carboxysteroids; Epristeride; Finasteride; Testosterone
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Indexed keywords
17 OXO 17A AZA D HOMO 3,5 ANDROSTADIEN 3 OIC ACID;
17 OXO 19 NOR 3,5 ANDROSTADIEN 3 OIC ACID;
17A (2 PROPIONOXYETHYL) 17 OXO 17A AZA D HOMO 3,5 ANDROSTADIEN 3 OIC ACID;
17A ACETYL 17 OXO 17A AZA D HOMO 3,5 ANDROSTADIEN 3 OIC ACID;
17A ACETYL 3 CYANO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
17A BENZOYL 3 CYANO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
17A ETHYL 17 OXO 17A AZA D HOMO 3,5 ANDROSTADIEN 3 OIC ACID;
17A ETHYL 3 CYANO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
17A METHYL 17 OXO 17A AZA D HOMO 3,5 ANDROSTADIEN 3 OIC ACID;
17A METHYL 3 CYANO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
3 BROMO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
3 BROMO 19 NOR 3,5 ANDROSTADIEN 17 ONE;
3 CYANO 17A AZA D HOMO 3,5 ANDROSTADIEN 17 ONE;
3 CYANO 19 NOR 3,5 ANDROSTADIEN 17 ONE;
ANDROSTANE DERIVATIVE;
FINASTERIDE;
PRASTERONE ACETATE;
STEROID 5ALPHA REDUCTASE 2;
STEROID 5ALPHA REDUCTASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ARTICLE;
CELL STRAIN HEK293;
DRUG POTENCY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
EVALUATION;
HUMAN;
HUMAN CELL;
IC 50;
MALE;
NONHUMAN;
PROSTATE;
RAT;
STRUCTURE ACTIVITY RELATION;
SUBSTITUTION REACTION;
5-ALPHA REDUCTASE INHIBITORS;
ANDROSTENEDIONE;
ANIMALS;
CHEMISTRY TECHNIQUES, SYNTHETIC;
CHOLESTENONE 5 ALPHA-REDUCTASE;
HEK293 CELLS;
HUMANS;
INHIBITORY CONCENTRATION 50;
ISOENZYMES;
MALE;
ORGAN SIZE;
PROSTATE;
RATS;
RATS, WISTAR;
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EID: 84864413353
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2012.06.026 Document Type: Article |
Times cited : (22)
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References (38)
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