Literature DB >> 12434991

Microbial transformation of (+)-adrenosterone.

S Ghulam Musharraf1, M Iqbal Choudhary, Sadia Sultan.   

Abstract

The microbial transformation of (+)-adrenosterone (1) by Cephalosporium aphidicola afforded three metabolites identified as androsta-1,4-diene-3,11,17-trione (2), 17beta-hydroxyandrost-4-ene-3,11-dione (3) and 17beta-hydroxyandrosta-1,4-diene-3,11-dione (4). The fermentation of 1 with Fusarium lini also produced metabolites 2 and 4, while the fermentation with Trichothecium roseum afforded metabolite 3. The structures of transformed products were determined by spectroscopic methods.

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Year:  2002        PMID: 12434991     DOI: 10.1080/10575630290033105

Source DB:  PubMed          Journal:  Nat Prod Lett        ISSN: 1026-8049


  2 in total

1.  Structure and absolute configuration of 20β-Hydroxyprednisolone, a biotransformed product of predinisolone by the marine endophytic fungus Penicilium lapidosum.

Authors:  Sadia Sultan; Muhammad Zaimi Bin Mohd Noor; El Hassane Anouar; Syed Adnan Ali Shah; Fatimah Salim; Rohani Rahim; Zuhra Bashir Khalifa Al Trabolsy; Jean-Frédéric Faizal Weber
Journal:  Molecules       Date:  2014-09-03       Impact factor: 4.411

2.  Isaria fumosorosea KCh J2 Entomopathogenic Strain as an Effective Biocatalyst for Steroid Compound Transformations.

Authors:  Ewa Kozłowska; Monika Dymarska; Edyta Kostrzewa-Susłow; Tomasz Janeczko
Journal:  Molecules       Date:  2017-09-09       Impact factor: 4.411

  2 in total

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