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[Secondary metabolites of Streptomyces sp. A1693].
Liu, Zhi-Guo; Tang, Meng-Yue; Meng, Qing-Hong; Zhang, Cun; Sun, Yi.
Afiliação
  • Liu ZG; Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
  • Tang MY; Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
  • Meng QH; College of Biotechnology, Tianjin University of Science & Technology, Tianjin 300457, China.
  • Zhang C; Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
  • Sun Y; School of Traditional Chinese Medica, Shengyang Pharmaceutical University, Shenyang 110016, China.
Zhongguo Zhong Yao Za Zhi ; 43(16): 3301-3306, 2018 Aug.
Article em Zh | MEDLINE | ID: mdl-30200733
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).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Streptomyces / Dicetopiperazinas Limite: Humans Idioma: Zh Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Streptomyces / Dicetopiperazinas Limite: Humans Idioma: Zh Ano de publicação: 2018 Tipo de documento: Article