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Journal Abstract Search

138 related items for PubMed ID: 15516742

  • 1.
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  • 2. Active-site-directed inactivation of aromatase from human placental microsomes by brominated androgen derivatives.
    Bellino FL, Gilani SS, Eng SS, Osawa Y, Duax WL.
    Biochemistry; 1976 Oct 19; 15(21):4730-6. PubMed ID: 974087
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  • 3. Synthesis and structure-activity relationships of 6-phenylaliphatic-substituted C19 steroids having a 1,4-diene, 4,6-diene, or 1,4,6-triene structure as aromatase inhibitors.
    Numazawa M, Yamaguchi S.
    Steroids; 1999 Mar 19; 64(3):187-96. PubMed ID: 10400379
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  • 4. Probing the binding pocket of the active site of aromatase with 6-ether or 6-ester substituted androst-4-ene-3,17-diones and their diene and triene analogs.
    Numazawa M, Shelangouski M, Nagasaka M.
    Steroids; 2000 Dec 19; 65(12):871-82. PubMed ID: 11077085
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  • 6. Gas chromatography-mass spectrometric study of 19-oxygenation of the aromatase inhibitor 19-methylandrostenedione with human placental microsomes.
    Numazawa M, Nagaoka M, Handa W, Yamada A.
    Biol Pharm Bull; 2006 Jun 19; 29(6):1242-5. PubMed ID: 16755025
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  • 7. Studies of the time-dependent inactivation of aromatase by 4beta,5beta-epoxy-6-one and 5beta,6beta-epoxy-4-one steroids under various conditions.
    Numazawa M, Yamada K.
    Biol Pharm Bull; 1999 Nov 19; 22(11):1207-11. PubMed ID: 10598029
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  • 8. Time-dependent aromatase inactivation by 4 beta,5 beta-epoxides of the natural substrate androstenedione and its 19-oxygenated analogs.
    Numazawa M, Yoshimura A, Tachibana M, Shelangouski M, Ishikawa M.
    Steroids; 2002 Mar 19; 67(3-4):185-93. PubMed ID: 11856542
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  • 9. Time-dependent inactivation of aromatase by 6-alkylandrosta-1,4-diene-3,17-diones. Effects of length and configuration of 6-alkyl group.
    Numazawa M, Oshibe M, Yamaguchi S, Tachibana M.
    J Med Chem; 1996 Mar 01; 39(5):1033-8. PubMed ID: 8676338
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  • 13. 6beta,19-Bridged androstenedione analogs as aromatase inhibitors.
    Komatsu S, Yaguchi A, Yamashita K, Nagaoka M, Numazawa M.
    Steroids; 2009 Nov 01; 74(12):884-9. PubMed ID: 19524602
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  • 14. Studies directed toward a mechanistic evaluation of aromatase inhibition by androst-5-ene-7,17-dione. Time-dependent inactivation by the 19-nor and 5 beta, 6 beta-epoxy derivatives.
    Numazawa M, Tachibana M.
    Steroids; 1997 Jul 01; 62(7):516-22. PubMed ID: 9253790
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  • 15. Aromatase inhibition by 4 beta,5 beta-epoxides of 16 alpha-hydroxyandrostenedione and its 19-oxygenated analogs, potential precursors of estriol production in the feto-placental unit.
    Numazawa M, Yoshimura A, Watari Y, Matsuzaki H.
    Biol Pharm Bull; 2002 Dec 01; 25(12):1566-9. PubMed ID: 12499641
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  • 16. Synthesis of 2,2-dimethyl-4-hydroxy-4-androstene-3,17-dione as an inhibitor of aromatase.
    Furth PS, Rosenberger J, Marcotte PA, Robinson CH.
    J Enzyme Inhib; 1990 Dec 01; 4(2):131-5. PubMed ID: 2098519
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  • 18. 6-Phenylaliphatic-substituted androst-4-ene-3,17-diones as aromatase inhibitors: structure-activity relationships.
    Numazawa M, Yamaguchi S.
    J Steroid Biochem Mol Biol; 1998 Oct 01; 67(1):41-8. PubMed ID: 9780028
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  • 19. Structure-activity relationships of 2alpha-substituted androstenedione analogs as aromatase inhibitors and their aromatization reactions.
    Numazawa M, Handa W, Hasegawa C, Takahashi M.
    J Steroid Biochem Mol Biol; 2005 Dec 01; 97(4):353-9. PubMed ID: 16209922
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