Literature DB >> 14577687

Microbial transformation of cortisol and prolyl endopeptidase inhibitory activity of its transformed products.

M Iqbal Choudhary1, Sadia Sultan, Muhammad Yaqoob, S Ghulam Musharraf, Amsha Yasin, Farzana Shaheen.   

Abstract

Incubation of cortisol (1) with Gibberella fujikuruoi for 12 days yielded an oxidatively cleaved product, 11beta-hydroxyandrost-4-en-3,17-dione (2), while incubation with Bacillus subtilis and Rhizopus stolonifer yielded the reduced product, 11beta, 17alpha,20,21-tetrahydroxy-(20S)-pregn-4-en-3-one (3). Other reduced products, 11beta, 17alpha, 21-trihydroxy-5alpha-pregnan-3, 20-dione (4) and 3beta, 11beta, 17alpha, 21-tetrahydroxy-5alpha-pregnan-20-one (5) were obtained by incubation of compound 1 with Bacillus cerus. The inhibitory activity of compounds 1-5 against prolyl endopeptidase enzyme (PEP) was also assayed. Compounds 2 (IC50 162.8 microM) and 4 (IC50 157 microM) have shown significant inhibitory activity against PEP.

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Year:  2003        PMID: 14577687     DOI: 10.1080/14786410310001617640

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


  1 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

  1 in total

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