Literature DB >> 15595610

Biotransformation of (+)-androst-4-ene-3,17-dione.

M Iqbal Choudhary1, Sadia Sultan, Mahmmud Tareq Hassan Khan, Amsha Yasin, Farzana Shaheen.   

Abstract

Fermentation of (+)-androst-4-ene-3,17-dione (1) with Curvularia lunata for 10 days yielded five oxidative and reductive metabolites, androsta-1,4-diene-3,17-dione (2), 17beta-hydroxyandrosta-1,4-dien-3-one (3), 11alpha-hydroxyandrost-4-ene-3,17-dione (4), 11alpha,17beta-dihydroxyandrost-4-en-3-one (5) and 15alpha-hydroxyandrosta-1,4-dien-17-one (6). The structures of these metabolites were elucidated on the basis of spectroscopic techniques. These microbially transformed products were assayed against the clinically important enzymes, tyrosinase and prolyl endopeptidase.

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Year:  2004        PMID: 15595610     DOI: 10.1080/14786410310001620628

Source DB:  PubMed          Journal:  Nat Prod Res        ISSN: 1478-6419            Impact factor:   2.861


  5 in total

1.  Fungal transformation of androsta-1,4-diene-3,17-dione by Aspergillus brasiliensis.

Authors:  Tahereh Hosseinabadi; Hossein Vahidi; Bahman Nickavar; Farzad Kobarfard
Journal:  Daru       Date:  2014-11-15       Impact factor: 3.117

2.  New Anti-Inflammatory Metabolites by Microbial Transformation of Medrysone.

Authors:  Saira Bano; Atia-Tul- Wahab; Sammer Yousuf; Almas Jabeen; Mohammad Ahmed Mesaik; Atta-Ur- Rahman; M Iqbal Choudhary
Journal:  PLoS One       Date:  2016-04-22       Impact factor: 3.240

3.  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

4.  Biotransformation of Androstenedione by Filamentous Fungi Isolated from Cultural Heritage Sites in the State Tretyakov Gallery.

Authors:  Alexander A Zhgun; Mark P Potapov; Darya A Avdanina; Natalya V Karpova; Vera V Yaderets; Vakhtang V Dzhavakhiya; Dmitry A Kardonsky
Journal:  Biology (Basel)       Date:  2022-06-08

5.  Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone.

Authors:  Salman Zafar; M Iqbal Choudhary; Kourosh Dalvandi; Uzma Mahmood; Zaheer Ul-Haq
Journal:  Chem Cent J       Date:  2013-10-08       Impact factor: 4.215

  5 in total

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