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Volumn 17, Issue 3, 2002, Pages 155-165
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Androsterone derivatives substituted at position 16: Chemical synthesis, inhibition of type 3 17β-hydroxysteroid dehydrogenase, binding affinity for steroid receptors and proliferative/antiproliferative activity on Shionogi (AR+) cells
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Author keywords
Androsterone; Biosynthesis; Enzyme; Hormones; Inhibitors; Steroids
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Indexed keywords
16,16 BIS(6' BROMOHEXYL) 3ALPHA HYDROXY 5ALPHA ANDROSTAN 17 ONE;
16,16 DIMETHYL 3ALPHA METHOXY 5ALPHA ANDROSTAN 17 ONE;
16ALPHA (3' BROMOPROPYL) 3ALPHA HYDROXY 5ALPHA ANDROSTAN 17 ONE;
16ALPHA (3' BROMOPROPYL) 5ALPHA ANDROSTANE 3ALPHA,17BETA DIOL;
16BETA (3' BROMOPROPYL) 3ALPHA HYDROXY 5ALPHA ANDROSTAN 17 ONE;
3ALPHA (ALLYLOXY) 16,16 DIALLYL 5ALPHA ANDROSTAN 17 ONE;
3ALPHA HYDROXY 16 SPIROCYCLOHEPTYL 5ALPHA ANDROSTAN 17 ONE;
3ALPHA HYDROXY 16 SPIROCYCLOHEXYL 5ALPHA ANDROSTAN 17 ONE;
3ALPHA HYDROXY 16,16 DIALLYL 5ALPHA ANDROSTAN 17 ONE;
3ALPHA HYDROXY 16,16 DIMETHYL 5ALPHA ANDROSTAN 17 ONE;
ALLYL COMPOUND;
ANDROGEN;
ANDROGEN RECEPTOR;
ANDROSTANOLONE;
ANDROSTENEDIONE;
ANDROSTERONE;
ANDROSTERONE DERIVATIVE;
DEXAMETHASONE;
ESTRADIOL;
ESTROGEN RECEPTOR;
ETHER DERIVATIVE;
GLUCOCORTICOID RECEPTOR;
HYDROXYFLUTAMIDE;
METHYL DERIVATIVE;
PROGESTERONE DERIVATIVE;
PROGESTERONE RECEPTOR;
R 5050;
STEROID RECEPTOR;
TESTOSTERONE;
TESTOSTERONE 17BETA DEHYDROGENASE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
17BETA HYDROXYSTEROID DEHYDROGENASE TYPE 3;
17BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 3;
ENZYME INHIBITOR;
HYDROXYSTEROID DEHYDROGENASE;
ARTICLE;
BINDING AFFINITY;
CELL PROLIFERATION;
CHEMICAL REACTION;
CONCENTRATION (PARAMETERS);
CONTROLLED STUDY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
ANIMAL;
CELL CULTURE;
CELL DIVISION;
CHEMISTRY;
DRUG ANTAGONISM;
DRUG EFFECT;
GENETIC TRANSFECTION;
GENETICS;
METABOLISM;
MOUSE;
PROTEIN BINDING;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
17-HYDROXYSTEROID DEHYDROGENASES;
ANDROSTERONE;
ANIMALS;
CELL DIVISION;
ENZYME INHIBITORS;
HUMANS;
MICE;
PROTEIN BINDING;
RECEPTORS, STEROID;
STRUCTURE-ACTIVITY RELATIONSHIP;
TRANSFECTION;
TUMOR CELLS, CULTURED;
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EID: 0036614094
PISSN: 14756366
EISSN: None
Source Type: Journal
DOI: 10.1080/1475636021000002067 Document Type: Article |
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Times cited : (15)
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References (33)
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