Literature DB >> 4832757

Isolation and identification of cerebrosides from the marine sponge Chondrilla nucula.

F J Schmitz, F J McDonald.   

Abstract

A cerebroside mixture has been isolated from the marine sponge Chondrilla nucula. Acid-catalyzed methanolysis of this cerebroside mixture afforded methyl glucosides, three long-chain bases, and a mixture of alpha-hydroxy fatty acid methyl esters. The bases were identified as saturated C(17), C(18), and C(19) trihydroxy bases (1,3,4-trihydroxy-2-aminoalkanes) by gas-liquid chromatographic-mass spectrometric analysis of their corresponding trimethylsilyl derivatives. The methyl ester fraction consisted of a mixture of homologous C(16) to C(26) saturated straight-chain alpha-hydroxy esters plus a trace of saturated C(25) iso alpha-hydroxy ester.

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Year:  1974        PMID: 4832757

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  4 in total

1.  First natural analogs of the cytotoxic thiodepsipeptide thiocoraline A from a marine Verrucosispora sp.

Authors:  Thomas P Wyche; Yanpeng Hou; Doug Braun; Hannah C Cohen; May P Xiong; Tim S Bugni
Journal:  J Org Chem       Date:  2011-07-20       Impact factor: 4.354

2.  Phylogenetic dichotomy of nerve glycosphingolipids.

Authors:  N Okamura; M Stoskopf; F Hendricks; Y Kishimoto
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

3.  A genetic model for the evolution of the glycosphingolipids.

Authors:  A R Rushton
Journal:  J Mol Evol       Date:  1975-10-03       Impact factor: 2.395

4.  2-Hydroxy fatty acids from marine sponges. 2. The phospholipid fatty acids of the Caribbean sponges Verongula gigantea and Aplysina archeri.

Authors:  N M Carballeira; F Shalabi; V Negrón
Journal:  Lipids       Date:  1989-03       Impact factor: 1.880

  4 in total

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