[Secondary metabolites of Streptomyces sp. A1693]

Zhongguo Zhong Yao Za Zhi. 2018 Aug;43(16):3301-3306. doi: 10.19540/j.cnki.cjcmm.20180510.008.
[Article in Chinese]

Abstract

By means of various chromatographic methods such as Sephadex LH-20,ODS,and semi-preparative HPLC,ten compounds were isolated from Streptomyces sp. A1693 and their structures were elucidated on the basis of spectroscopic data and physico-chemical methods. The compounds comprised 5 butenolides,2 diketopiperazines,and 3 antimycin antibiotics. The structures were identified as (5S)-5-(11-hydroxymethyloctyl)furan-2(5H)-one (1), (5S)-5-(11-hydroxy-11-methylheptyl)furan-2(5H)-one (2), (5S)-5-(11-methyl-12-oxooctyl) furan-2(5H)-one (3), (5S)-5-(11-hydroxy-11-methyloctyl)furan-2(5H)-one (4), (5S)-5-(11-hydroxy-12-methyloctyl)furan-2(5H)-one(5),cyclo-Phe-Val (6),cyclo-Phe-Ile (7),uranchimycin A (8),uranchimycin B (9),and deisovalerylblastomycin (10). Among them,1 was defined as a new compound. All the compounds didn't show the cytotoxic activity against A549 cell line (IC₅₀>50 mg·L⁻¹).

Keywords: Streptomyces sp.; butenolides; cytotoxic activity; secondary metabolites.

MeSH terms

  • A549 Cells
  • Diketopiperazines / chemistry*
  • Furans / chemistry
  • Humans
  • Secondary Metabolism
  • Streptomyces / chemistry*

Substances

  • Diketopiperazines
  • Furans