Literature DB >> 16061265

Stemodane and stemarane diterpenoid hydroxylation by Mucor plumbeus and Whetzelinia sclerotiorum.

Avril R M Chen1, Peter L D Ruddock, Andrew S Lamm, William F Reynolds, Paul B Reese.   

Abstract

Incubation of stemodin (1) with Mucor plumbeus ATCC 4740 resulted in the formation of 2alpha,6beta,13-trihydroxystemodane (2), 2alpha,3beta,13-trihydroxystemodane (3), 2alpha,11beta,13-trihydroxystemodane (4) and 2alpha,13,14-trihydroxystemodane (5), while stemodinone (7) afforded 6alpha,13-dihydroxystemodan-2-one (8) and 6alpha,12alpha,13-trihydroxystemodan-2-one (9). Metabolites obtained from the bioconversion of stemarin (11) were 8,13,19-trihydroxystemarane (12) and 2alpha,13,19-trihydroxystemarane (13). 19-N,N-Dimethylcarbamoxy-13-hydroxystemarane (14) was not transformed by the fungus. Stemodin (1) was incubated with Whetzelinia sclerotiorum ATCC 18687 to produce 2alpha,7beta,13-trihydroxystemodane (6) and 2alpha,11beta,13-trihydroxystemodane (4). Stemodinone (7) was converted to 7beta,13-dihydroxystemodan-2-one (10). Compounds 2, 4, 9, 10, 12 and 13 have not been previously reported.

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Year:  2005        PMID: 16061265     DOI: 10.1016/j.phytochem.2005.06.015

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  2 in total

1.  Biotransformations of imbricatolic acid by Aspergillus niger and Rhizopus nigricans cultures.

Authors:  Guillermo Schmeda-Hirschmann; Carlos Aranda; Marcela Kurina; Jaime A Rodríguez; Cristina Theoduloz
Journal:  Molecules       Date:  2007-05-21       Impact factor: 4.411

Review 2.  Stemodane Diterpenes and Diterpenoids: Isolation, Structure Elucidation, Biogenesis, Biosynthesis, Biological Activity, Biotransformations, Metabolites and Derivatives Biological Activity, Rearrangements.

Authors:  Francesca Leonelli; Luisa Maria Migneco; Alessio Valletta; Rinaldo Marini Bettolo
Journal:  Molecules       Date:  2021-05-07       Impact factor: 4.411

  2 in total

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