JOURNAL 520


Records of Natural Products
VOLUME & ISSUE
Year: 2015 Issue: 2 April-June
PAGES
p.196 - 200
STATISTICS
Viewed 2335 times.
AUTHORS
    Hao Zhou, Lixing Zhao, Wei Li, Yabin Yang, Lihua Xu and Zhongtao Ding
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


In our screening for antitubercular leading compounds, an endophytic Streptomyces sp. YIM65484 was selected by biological assay. Four bioactive metabolites were isolated from this strain. Their structures were determined as (2E,4E)-5-(3-hydroxyphenyl)- penta-2,4- dienamide (1), ergosterol (2), ergosterol peroxide (3) and halolitoralin B (4) by spectral analysis. Compound 1 is a new phenylpentadienamide with its rarely encountered skeleton in natural products. Compounds 1-4 showed selectivity for anti-M. Tuberculosis activity in comparison with other antimicrobial activity. Compound 4 was first isolated from Streptomyces.

KEYWORDS
  • Streptomyces sp.
  • anti- M. tuberculosis
  • phenylpentadienamide

SUPPORTING INFORMATION


Supporting Information
Download File 21-RNP-1405-095-SI.pdf (662.85 KB)