|
Volumn 45, Issue 16, 2002, Pages 3406-3417
|
Synthesis and evaluation of 2′-substituted 4-(4′-carboxy- or 4′-carboxymethylbenzylidene)-N-acylpiperidines: Highly potent and in vivo active steroid 5α-reductase type 2 inhibitors
|
Author keywords
[No Author keywords available]
|
Indexed keywords
BENZYLIDENE DERIVATIVE;
FINASTERIDE;
ISOENZYME;
N (DICYCLOHEXYL)ACETYLPIPERIDINE 4 (2 FLUOROBENZYLIDENE 4 CARBOXYLIC ACID);
N (DICYCLOHEXYL)ACETYLPIPERIDINE 4 (BENZYLIDENE 4 ACETIC ACID);
PIPERIDINE DERIVATIVE;
STEROID 5ALPHA REDUCTASE;
STEROID 5ALPHA REDUCTASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ARTICLE;
CASTRATION;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME INHIBITION;
FLUORINATION;
HUMAN;
HUMAN CELL;
IC 50;
MALE;
NONHUMAN;
PROSTATE;
RAT;
STRUCTURE ACTIVITY RELATION;
ANIMALS;
BENZOIC ACIDS;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
ENZYME INHIBITORS;
HUMANS;
ISOENZYMES;
MALE;
MODELS, MOLECULAR;
ORCHIECTOMY;
ORGAN SIZE;
PIPERIDINES;
PROSTATE;
RATS;
STRUCTURE-ACTIVITY RELATIONSHIP;
TESTOSTERONE;
TESTOSTERONE 5-ALPHA-REDUCTASE;
|
EID: 0036682372
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm0208471 Document Type: Article |
Times cited : (26)
|
References (40)
|