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Journal Abstract Search


132 related items for PubMed ID: 8439517

  • 21. The enzyme and inhibitors of 4-ene-3-oxosteroid 5 alpha-oxidoreductase.
    Li X, Chen C, Singh SM, Labrie F, Labire F [corrected to Labrie F].
    Steroids; 1995 Jun; 60(6):430-41. PubMed ID: 7676475
    [Abstract] [Full Text] [Related]

  • 22. FCE 28260, a new 5 alpha-reductase inhibitor: in vitro and in vivo effects.
    Giudici D, Briatico G, Cominato C, Zaccheo T, Iehlè C, Nesi M, Panzeri A, di Salle E.
    J Steroid Biochem Mol Biol; 1996 Jun; 58(3):299-305. PubMed ID: 8836165
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  • 23. Novel aromatase and 5 alpha-reductase inhibitors.
    Di Salle E, Briatico G, Giudici D, Ornati G, Zaccheo T, Buzzetti F, Nesi M, Panzeri A.
    J Steroid Biochem Mol Biol; 1994 Jun; 49(4-6):289-94. PubMed ID: 8043491
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  • 24. The clinical development of a 5 alpha-reductase inhibitor, finasteride.
    Stoner E.
    J Steroid Biochem Mol Biol; 1990 Nov 20; 37(3):375-8. PubMed ID: 1701660
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  • 27. Pharmacokinetics and biochemical efficacy after single and multiple oral administration of N-(2-methyl-2-propyl)-3-oxo-4-aza-5 alpha-androst-1-ene-17 beta-carboxamide, a new type of specific competitive inhibitor of testosterone 5 alpha-reductase, in volunteers.
    Ohtawa M, Morikawa H, Shimazaki J.
    Eur J Drug Metab Pharmacokinet; 1991 Nov 20; 16(1):15-21. PubMed ID: 1657611
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  • 30. Azasteroids as inhibitors of rat prostatic 5 alpha-reductase.
    Rasmusson GH, Reynolds GF, Utne T, Jobson RB, Primka RL, Berman C, Brooks JR.
    J Med Chem; 1984 Dec 20; 27(12):1690-701. PubMed ID: 6502599
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  • 32. MK-386, an inhibitor of 5alpha-reductase type 1, reduces dihydrotestosterone concentrations in serum and sebum without affecting dihydrotestosterone concentrations in semen.
    Schwartz JI, Tanaka WK, Wang DZ, Ebel DL, Geissler LA, Dallob A, Hafkin B, Gertz BJ.
    J Clin Endocrinol Metab; 1997 May 20; 82(5):1373-7. PubMed ID: 9141518
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  • 34. Delta 5-3 beta-hydroxysteroid dehydrogenase-isomerase activity in two distinct density Leydig cells from immature rats. Differences in responsiveness to human chorionic gonadotropin or 8-bromoadenosine 3',5'-monophosphate.
    Murono EP, Washburn AL.
    Biochim Biophys Acta; 1991 Jan 10; 1091(1):55-62. PubMed ID: 1847300
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  • 36. Mechanism of time-dependent inhibition of 5 alpha-reductases by delta 1-4-azasteroids: toward perfection of rates of time-dependent inhibition by using ligand-binding energies.
    Tian G, Mook RA, Moss ML, Frye SV.
    Biochemistry; 1995 Oct 17; 34(41):13453-9. PubMed ID: 7577933
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  • 37. Four-amino acid segment in steroid 5 alpha-reductase 1 confers sensitivity to finasteride, a competitive inhibitor.
    Thigpen AE, Russell DW.
    J Biol Chem; 1992 Apr 25; 267(12):8577-83. PubMed ID: 1314830
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  • 39. Effects of 4-MA, a potent inhibitor of 5 alpha-reductase, on 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase activity in guinea pig adrenals.
    Perron S, Bélanger A.
    Steroids; 1994 Jun 25; 59(6):371-6. PubMed ID: 7940615
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