4.4 Article

Syn-2, 3-diols and anti-inflammatory indole derivatives from Streptomyces sp. CB09001

Journal

NATURAL PRODUCT RESEARCH
Volume 35, Issue 1, Pages 144-151

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14786419.2019.1611812

Keywords

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Funding

  1. NSFC [81473124]
  2. Chinese Ministry of Education 111 Project [B0803420]
  3. Hunan Graduate Research and Innovation Grant [CX2018B049]

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Two new natural diols and five known compounds were isolated from Streptomyces sp. CB09001, with their absolute configurations established by crystallographic structure analysis. One of the compounds showed significant inhibition of inducible nitric oxide synthase expression in macrophage cells and could be a potential lead for anti-inflammatory drug development.
Two new natural diols, (2S, 3S, 4S)-4-methyl-1-phenylhexane-2,3-diol (1) and (2S, 3S)-4-methyl-1-phenylpentane-2,3-diol (2), together with five known compounds, xenocyloins B-D (3-5), lumichrome (6) and thymidine (7) were isolated from Streptomyces sp. CB09001. The absolute configurations of 1 and 2 were established by crystallographic structure analysis. The anti-inflammatory effects of 1-7 were also investigated in RAW246.7 murine macrophage cells stimulated by lipopolysaccharide. The indole derivative xenocyloin B (3) significantly inhibited inducible nitric oxide synthase expression in RAW264.7 cells and could be a potential anti-inflammatory drug lead.

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