Literature DB >> 18044808

Complete 1H and 13C NMR assignments of three new polyhydroxylated sterols from the South China Sea gorgonian Subergorgia suberosa.

Shu-Hua Qi1, Si Zhang, Yi-Fei Wang, Ming-Yi Li.   

Abstract

Three new polyhydroxylated sterols, 3beta,6alpha,11,20beta,24-pentahydroxy- 9,11-seco-5alpha-24-ethylcholest-7,28-diene-9-one (1), 3-(1',2'-ethandiol)-24- methylcholest-8(9),22E-diene-3beta,5alpha,6alpha,7alpha,11alpha-pentaol (2), 24-methylcholest-7,22 E-diene-3beta,5alpha,6beta,25-tetraol (3) together with five known sterols, were isolated from the EtOH/CH2Cl2 extract of the South China Sea gorgonian Subergorgia suberosa. The complete assignments of the 1H and 13C NMR chemical shifts for these new compounds were achieved by means of 1D and 2D NMR techniques, including HSQC, HMBC, 1H--1H COSY, and NOESY spectra. Copyright (c) 2007 John Wiley & Sons, Ltd.

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Year:  2007        PMID: 18044808     DOI: 10.1002/mrc.2102

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  2 in total

1.  Chemical constituents and biological activities of the genus Subergorgia.

Authors:  Faheem Amir; Wan Sinn Yam; Yen Chin Koay
Journal:  Pharmacogn Rev       Date:  2012-01

2.  Ergosterols from the Culture Broth of Marine Streptomyces anandii H41-59.

Authors:  Yang-Mei Zhang; Hong-Yu Li; Chen Hu; Hui-Fan Sheng; Ying Zhang; Bi-Run Lin; Guang-Xiong Zhou
Journal:  Mar Drugs       Date:  2016-05-04       Impact factor: 5.118

  2 in total

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