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Journal Abstract Search


156 related items for PubMed ID: 16736172

  • 1. Studies on the microbial transformation of androst-1,4-dien-3,17-dione with Acremonium strictum.
    Faramarzi MA, Yazdi MT, Jahandar H, Amini M, Monsef-Esfahani HR.
    J Ind Microbiol Biotechnol; 2006 Sep; 33(9):725-33. PubMed ID: 16736172
    [Abstract] [Full Text] [Related]

  • 2. Metabolism of androst-4-en-3,17-dione by the filamentous fungus Neurospora crassa.
    Faramarzi MA, Aghelnejad M, Tabatabaei Yazdi M, Amini M, Hajarolasvadi N.
    Steroids; 2008 Jan; 73(1):13-8. PubMed ID: 17981313
    [Abstract] [Full Text] [Related]

  • 3. Biocatalyst-mediated production of 11,15-dihydroxy derivatives of androst-1,4-dien-3,17-dione.
    Qiao Y, Shen Y, Huang W, Wang Y, Ren J, Xia T, Wang M.
    J Biosci Bioeng; 2017 Jun; 123(6):692-697. PubMed ID: 28215508
    [Abstract] [Full Text] [Related]

  • 4. Microbial transformation of nandrolone decanoate by acremonium strictum.
    Yazdi MT, Zanjanian SM, Faramarzi MA, Amini M, Amani A, Abdi K.
    Arch Pharm (Weinheim); 2006 Aug; 339(8):473-6. PubMed ID: 16832817
    [Abstract] [Full Text] [Related]

  • 5. Microbial transformation of (+)-androsta-1 ,4-diene-3,17-dione by Cephalosporium aphidicola.
    Choudhary MI, Musharraf SG, Shaheen F, Atta-Ur-Rahman.
    Nat Prod Lett; 2002 Dec; 16(6):377-82. PubMed ID: 12462341
    [Abstract] [Full Text] [Related]

  • 6. Microbial transformation of hydrocortisone by Acremonium strictum PTCC 5282.
    Faramarzi MA, Yazdi MT, Shafiee A, Zarrini G.
    Steroids; 2002 Sep; 67(10):869-72. PubMed ID: 12231122
    [Abstract] [Full Text] [Related]

  • 7. Fungal transformation of androsta-1,4-diene-3,17-dione by Aspergillus brasiliensis.
    Hosseinabadi T, Vahidi H, Nickavar B, Kobarfard F.
    Daru; 2014 Nov 15; 22(1):71. PubMed ID: 25398302
    [Abstract] [Full Text] [Related]

  • 8. Microbial transformation of androst-4-ene-3,17-dione by Beauveria bassiana.
    Xiong Z, Wei Q, Chen H, Chen S, Xu W, Qiu G, Liang S, Hu X.
    Steroids; 2006 Nov 15; 71(11-12):979-83. PubMed ID: 16973198
    [Abstract] [Full Text] [Related]

  • 9. Microbial transformation of 17alpha-ethynyl- and 17alpha-ethylsteroids, and tyrosinase inhibitory activity of transformed products.
    Choudhary MI, Sultan S, Khan MT, Rahman AU.
    Steroids; 2005 Nov 15; 70(12):798-802. PubMed ID: 16054181
    [Abstract] [Full Text] [Related]

  • 10. Biotransformation of (+)-androst-4-ene-3,17-dione.
    Choudhary MI, Sultan S, Khan MT, Yasin A, Shaheen F, Atta-ur-Rahman.
    Nat Prod Res; 2004 Dec 15; 18(6):529-35. PubMed ID: 15595610
    [Abstract] [Full Text] [Related]

  • 11. Microbial hydroxylation of progesterone with Acremonium strictum.
    Faramarzi MA, Tabatabaei Yazdi M, Amini M, Zarrini G, Shafiee A.
    FEMS Microbiol Lett; 2003 May 28; 222(2):183-6. PubMed ID: 12770705
    [Abstract] [Full Text] [Related]

  • 12. Studies on Bacillus stearothermophilus. Part III. Transformation of testosterone.
    Al-Awadi S, Afzal M, Oommen S.
    Appl Microbiol Biotechnol; 2003 Jul 28; 62(1):48-52. PubMed ID: 12835920
    [Abstract] [Full Text] [Related]

  • 13. Synthesis of 3beta-hydroxy-androsta-5,7-dien-17-one from 3beta-hydroxyandrost-5-en-17-one via microbial 7alpha-hydroxylation.
    Lobastova TG, Khomutov SM, Vasiljeva LL, Lapitskaya MA, Pivnitsky KK, Donova MV.
    Steroids; 2009 Feb 28; 74(2):233-7. PubMed ID: 19071148
    [Abstract] [Full Text] [Related]

  • 14. Biotransformation of androstenedione and androstadienedione by selected Ascomycota and Zygomycota fungal strains.
    Kollerov V, Shutov A, Kazantsev A, Donova M.
    Phytochemistry; 2020 Jan 28; 169():112160. PubMed ID: 31600654
    [Abstract] [Full Text] [Related]

  • 15. Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone.
    Zafar S, Choudhary MI, Dalvandi K, Mahmood U, Ul-Haq Z.
    Chem Cent J; 2013 Oct 08; 7(1):164. PubMed ID: 24103815
    [Abstract] [Full Text] [Related]

  • 16. Metabolism of metandienone in man: identification and synthesis of conjugated excreted urinary metabolites, determination of excretion rates and gas chromatographic-mass spectrometric identification of bis-hydroxylated metabolites.
    Schänzer W, Geyer H, Donike M.
    J Steroid Biochem Mol Biol; 1991 Apr 08; 38(4):441-64. PubMed ID: 2031859
    [Abstract] [Full Text] [Related]

  • 17. A mutant form of 3-ketosteroid-Δ(1)-dehydrogenase gives altered androst-1,4-diene-3, 17-dione/androst-4-ene-3,17-dione molar ratios in steroid biotransformations by Mycobacterium neoaurum ST-095.
    Shao M, Zhang X, Rao Z, Xu M, Yang T, Li H, Xu Z, Yang S.
    J Ind Microbiol Biotechnol; 2016 May 08; 43(5):691-701. PubMed ID: 26886757
    [Abstract] [Full Text] [Related]

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