Literature DB >> 11140523

Antialgal ent-labdane diterpenes from Ruppia maritima.

M DellaGreca1, A Fiorentino, M Isidori, P Monaco, A Zarrelli.   

Abstract

Seven ent-labdane diterpenes have been isolated from Ruppia maritima. The structures 15,16-epoxy-ent-labda-8(17),13(16),14-trien-19-al; 15,16-epoxy-ent-labda-8(17),13(16),14-trien-19-ol acetate; methyl 15,16-epoxy-12-oxo-ent-labda-8(17),13(16),14-trien-19-oate; 15,16-epoxy-ent-labd-8(17),13E-dien-15-ol and 13-oxo-15,16-bis-nor-ent-labd-8(17)-ene have been assigned to the five new compounds by spectroscopic means and chemical correlations. The phytotoxicity of the diterpenes has been assessed using the alga Selenastrum capricornutum as organism test.

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Year:  2000        PMID: 11140523     DOI: 10.1016/s0031-9422(00)00253-3

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


  2 in total

Review 1.  Chemical ecology of marine angiosperms: opportunities at the interface of marine and terrestrial systems.

Authors:  R Drew Sieg; Julia Kubanek
Journal:  J Chem Ecol       Date:  2013-05-18       Impact factor: 2.626

2.  Effect of ent-labdane diterpenes from Potamogetonaceae on Selenastrum capricornutum and other aquatic organisms.

Authors:  Tiziana Cangiano; Marina Dellagreca; Antonio Fiorentino; Marina Isidori; Pietro Monaco; Armando Zarrelli
Journal:  J Chem Ecol       Date:  2002-06       Impact factor: 2.626

  2 in total

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