Literature DB >> 17256903

Metabolites from the Lichen Ochrolechia parella growing under two different heliotropic conditions.

Marion Millot1, Sophie Tomasi, Kristina Articus, Isabelle Rouaud, Aurélie Bernard, Joël Boustie.   

Abstract

A new chloro-depsidone (1) and five known compounds, variolaric acid (2), lecanoric acid (3), alpha-alectoronic acid (4), atranorin (5), and ergosterol peroxide (6), have been isolated from the lichen Ochrolechia parella. The structure of compound 1 was elucidated by spectroscopic analysis. Additionally, the tautomeric equilibrium of compound 4 was investigated. In the present study, two specimens of this lichen, growing under different light conditions, were analyzed. The major compound in both samples was found to be 2, but the amount of this metabolite was significantly higher in the shaded specimen (0.76% w/w). The new compound parellin (1) predominated in the specimen grown under shady conditions, while atranorin (5) was found only in the sunlit specimen. The cytotoxic activities of 2, 4, and 6 against B16 melanoma cells were evaluated.

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Year:  2007        PMID: 17256903     DOI: 10.1021/np060561p

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  2 in total

1.  Discovery of depsides and depsidones from lichen as potent inhibitors of microsomal prostaglandin E2 synthase-1 using pharmacophore models.

Authors:  Julia Bauer; Birgit Waltenberger; Stefan M Noha; Daniela Schuster; Judith M Rollinger; Joel Boustie; Marylene Chollet; Hermann Stuppner; Oliver Werz
Journal:  ChemMedChem       Date:  2012-10-25       Impact factor: 3.466

2.  In Vitro Antileishmanial Activity of Sterols from Trametes versicolor (Bres. Rivarden).

Authors:  Vivian Leliebre-Lara; Lianet Monzote Fidalgo; Eva-Maria Pferschy-Wenzig; Olaf Kunert; Clara Nogueiras Lima; Rudolf Bauer
Journal:  Molecules       Date:  2016-08-10       Impact factor: 4.411

  2 in total

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