Literature DB >> 494359

Side chain-hydroxylated sterols of the red alga Asparagopsis armata: significant products or artifacts due to autoxidation?

C Francisco, G Combaut, J Teste, C Tarchini, C Djerassi.   

Abstract

Sterols characterized by an allylic hydroxyl group in the side chain, such as stigmasta-5,28-diene-3 beta, 24 epsilon-diol (1), cholesta-5,23-diene-3 beta,25-diol (2) and cholesta-5,25-diene-3 beta,24 epsilon-diol (3), have been identified several times in various marine algae. Their origin was considered as doubtful: they could have been bona fide constituents of the alga, or be artifacts caused by autoxidation during the isolation process. We have shown that the dihydroxy steroids 2 and 3 can indeed be produced by the autoxidation of cholesta-5,24-dien-3 beta-ol (desmosterol) (5), but that they are nevertheless present in the taxonomic significance.

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Year:  1979        PMID: 494359     DOI: 10.1016/0039-128x(79)90045-x

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  2 in total

Review 1.  Secondary Metabolites and Biological Activity of Invasive Macroalgae of Southern Europe.

Authors:  Patrícia Máximo; Luísa M Ferreira; Paula Branco; Pedro Lima; Ana Lourenço
Journal:  Mar Drugs       Date:  2018-08-02       Impact factor: 5.118

Review 2.  Asparagopsis Genus: What We Really Know About Its Biological Activities and Chemical Composition.

Authors:  José M S Ponte; Ana M L Seca; Maria Carmo Barreto
Journal:  Molecules       Date:  2022-03-09       Impact factor: 4.411

  2 in total

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