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Journal Abstract Search

111 related items for PubMed ID: 24455864

  • 1. [Effect of the steroid molecule structure on the direction of its hydroxylation by the fungus Curvularia lunata].
    Andriushina VA, Iaderets VV, Stytsenko TS, Druzhinina AV, Voĭshvillo NE.
    Prikl Biokhim Mikrobiol; 2013; 49(4):382-90. PubMed ID: 24455864
    [Abstract] [Full Text] [Related]

  • 2. [Properties of Rhizopus sp. cultures in the transformation of steroid compounds. II. 11-alpha hydroxylation of delta 4-3 ketosteroids of the pregnane and androstane group].
    Eysymontt I, Kotula W, Golonka J, Smolińska J, Iwaszkiewicz M.
    Acta Pol Pharm; 1975; 32(5):563-7. PubMed ID: 1199758
    [No Abstract] [Full Text] [Related]

  • 3. Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5 alpha-androstanes and 5 alpha-estranes with the fungus Rhizopus nigricans.
    Browne JW, Denny WA, Jones ER, Meakins GD, Morisawa Y, Pendlebury A, Pragnell J.
    J Chem Soc Perkin 1; 1973; 14():1493-9. PubMed ID: 4739028
    [No Abstract] [Full Text] [Related]

  • 4. Microbiological hydroxylation. Part XIX. The action of an ant fungus ('Acromyrmex fungus') on oxygenated androstanes, pregnanes, and cholestanes.
    Jones ER, Meakins GD, Miners JO, Pragnell JH, Wilkins AL.
    J Chem Soc Perkin 1; 1975; (16):1552-4. PubMed ID: 1236863
    [No Abstract] [Full Text] [Related]

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  • 7. [Bioconversion of C19- and C21-steroids with parent and mutant strains of Curvularia lunata].
    Kollerov VV, Shutov AA, Fokina VV, Sukhodol'skaia GV, Gulevskaia SA, Donova MV.
    Prikl Biokhim Mikrobiol; 2010; 46(2):212-20. PubMed ID: 20391766
    [Abstract] [Full Text] [Related]

  • 8. [7alpha-hydroxylation of steroid 5-olefins by mold fungi].
    Andriushina VG, Druzhinina AV, Iaderets VV, Stytsenko TS, Voĭshvillo NE.
    Prikl Biokhim Mikrobiol; 2010; 46(1):78-83. PubMed ID: 20198922
    [Abstract] [Full Text] [Related]

  • 9. [Microbiological hydroxylation of 5 ,6 -epoxy-3 -hydroxy-5 -pregnane-20-ones with further transformations].
    Cleve G, Hoyer GA, Kieslich K, Wieglepp H.
    Chem Ber; 1972; 105(2):658-72. PubMed ID: 4674912
    [No Abstract] [Full Text] [Related]

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  • 13. Microbiological hydroxylation of steroids. X. 1 beta, 11 alpha-dihydroxylation of 3 beta-hydroxy-5 alpha-prepnan-20-one and the hydroxylation of other 20-oxo-5 alpha-pregnanes with the fungus Aspergillys ochraceus.
    Clegg AS, Denny WA, Jones ER, Meakins GD, Pinhey JT.
    J Chem Soc Perkin 1; 1973; 19():2137-41. PubMed ID: 4796663
    [No Abstract] [Full Text] [Related]

  • 14. Reduction of the 20-carbonyl group of C-21 steroids by spores of Fusarium solani and other microorganisms. I. Side-chain degradation, epoxide cleavage, and substrate specificity.
    Plourde R, el-Tayeb OM, Hafez-Zedan H.
    Appl Microbiol; 1972 Mar; 23(3):601-12. PubMed ID: 5021973
    [Abstract] [Full Text] [Related]

  • 15. Microbiological hydroxylation. Part XVII. C-19 hydroxylation of 17-oxo-5alpha-androstanes and 17-oxo-3alpha, 5-cyclo-5alpha-androstanes by the fungus Calonectria decora.
    Chambers VE, Denny WA, Jones ER, Meakins GD, Miners JO, Pinhey JT, Wilkins AL.
    J Chem Soc Perkin 1; 1975 Mar; (14):1359-63. PubMed ID: 1172505
    [No Abstract] [Full Text] [Related]

  • 16. Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals.
    Bell AM, Clark IM, Denny WA, Jones ER, Meakins GD, Müller WE.
    J Chem Soc Perkin 1; 1973 Mar; 19():2131-6. PubMed ID: 4796662
    [No Abstract] [Full Text] [Related]

  • 17. Microbiological hydroxylation. Part XVII. Introduction of 16alpha-, 9alpha-, and 3alpha-hydroxy-groups into dioxygenated 5alpha-androstanes by the fungus Diaporthe celastrina.
    Bell AM, Boul AD, Jones ER, Meakins GD, Miners JO, Wilkins AL.
    J Chem Soc Perkin 1; 1975 Mar; (14):1364-6. PubMed ID: 1172506
    [No Abstract] [Full Text] [Related]

  • 18. Microbiological hydroxylation of steroids. V. The pattern of hydroxylation of dioxygenated 5 -androstanes with cultures of the fungus Calonectria decora.
    Bell AM, Denny WA, Jones ER, Meakins GD, Müller WE.
    J Chem Soc Perkin 1; 1972 Mar; 21():2759-65. PubMed ID: 4566120
    [No Abstract] [Full Text] [Related]

  • 19. [The active center of the 3-oxosteroid delta-1-dehydrogenase from Arthrobacter simplex (author's transl)].
    Pénasse L, Nomine G.
    Eur J Biochem; 1974 Sep 16; 47(3):555-9. PubMed ID: 4434996
    [No Abstract] [Full Text] [Related]

  • 20. Cytochrome P450 and steroid 21-hydroxylation in microsomes from human adrenal cortex.
    Lewis AM, Bryan GT.
    Life Sci II; 1971 Aug 22; 10(16):901-8. PubMed ID: 4398270
    [No Abstract] [Full Text] [Related]

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