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Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures

The present study reports the biotransformation of an anabolic-androgenic steroid (AAS) drostanolone heptanoate (1) by using two microbial cultures, Beauveria bassiana, and Macrophomina phaseolina. Fermentation of 1 with B. bassiana yielded five new transformed products 2–6, while with M. phaseolina...

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Detalles Bibliográficos
Autores principales: Hussain, Zahid, Atia-tul-Wahab, Hussain, Nusrat, Hussain, Shabbir, Atta-ur-Rahman, Choudhary, M. Iqbal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048210/
https://www.ncbi.nlm.nih.gov/pubmed/35492536
http://dx.doi.org/10.1039/c9ra05878h
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author Hussain, Zahid
Atia-tul-Wahab,
Hussain, Nusrat
Hussain, Shabbir
Atta-ur-Rahman,
Choudhary, M. Iqbal
author_facet Hussain, Zahid
Atia-tul-Wahab,
Hussain, Nusrat
Hussain, Shabbir
Atta-ur-Rahman,
Choudhary, M. Iqbal
author_sort Hussain, Zahid
collection PubMed
description The present study reports the biotransformation of an anabolic-androgenic steroid (AAS) drostanolone heptanoate (1) by using two microbial cultures, Beauveria bassiana, and Macrophomina phaseolina. Fermentation of 1 with B. bassiana yielded five new transformed products 2–6, while with M. phaseolina it afforded two new 7–8, and two known 9–10 metabolites. The main sites of hydroxylation in the steroidal skeleton of 1 were at C-5, C-7, C-11, C-14, C-15, and C-20, hydrolysis of the ester moiety at C-17, and reduction of the carbonyl group at C-3. The structures of the transformed products were determined by using mass, NMR, and other spectroscopic techniques.
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spelling pubmed-90482102022-04-28 Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures Hussain, Zahid Atia-tul-Wahab, Hussain, Nusrat Hussain, Shabbir Atta-ur-Rahman, Choudhary, M. Iqbal RSC Adv Chemistry The present study reports the biotransformation of an anabolic-androgenic steroid (AAS) drostanolone heptanoate (1) by using two microbial cultures, Beauveria bassiana, and Macrophomina phaseolina. Fermentation of 1 with B. bassiana yielded five new transformed products 2–6, while with M. phaseolina it afforded two new 7–8, and two known 9–10 metabolites. The main sites of hydroxylation in the steroidal skeleton of 1 were at C-5, C-7, C-11, C-14, C-15, and C-20, hydrolysis of the ester moiety at C-17, and reduction of the carbonyl group at C-3. The structures of the transformed products were determined by using mass, NMR, and other spectroscopic techniques. The Royal Society of Chemistry 2020-01-02 /pmc/articles/PMC9048210/ /pubmed/35492536 http://dx.doi.org/10.1039/c9ra05878h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Hussain, Zahid
Atia-tul-Wahab,
Hussain, Nusrat
Hussain, Shabbir
Atta-ur-Rahman,
Choudhary, M. Iqbal
Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title_full Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title_fullStr Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title_full_unstemmed Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title_short Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures
title_sort seven new metabolites of drostanolone heptanoate by using beauveria bassiana, and macrophomina phaseolina cell suspension cultures
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048210/
https://www.ncbi.nlm.nih.gov/pubmed/35492536
http://dx.doi.org/10.1039/c9ra05878h
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