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Suncheonosides E-M and Benzothioate Derivatives from the Marine-Derived Streptomyces sp. ZSN77.
Jiang, Miao; Zhang, Ying; Zhang, Yuxiao; Ma, Zhongjun; Wang, Jinhui.
  • Jiang M; Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, People's Republic of China.
  • Zhang Y; Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, People's Republic of China.
  • Zhang Y; Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, People's Republic of China.
  • Ma Z; Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, People's Republic of China.
  • Wang J; Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, People's Republic of China.
J Nat Prod ; 85(7): 1771-1778, 2022 07 22.
Article en En | MEDLINE | ID: mdl-35762988
ABSTRACT
Thirteen new compounds, including suncheonosides E-M (1-9), four benzothioate derivatives (10-13), and one known compound (14), were identified from the marine-derived Streptomyces sp. ZSN77. Suncheonosides E-M incorporate ß-d-glucose, while the reported suncheonosides (A-D) incorporate only l-rhamnose. All of the structures were determined by extensive analysis of NMR spectroscopic and HRESIMS data. Bioactivity evaluation of these compounds showed that 6 had significant activity against PC3 cells with an IC50 value of 4.1 ± 0.1 µM, while compounds 12 and 14 exhibited cytotoxicity against HCT116 cells with IC50 values of 7.3 ± 0.4 and 3.9 ± 0.3 µM, respectively. In addition, compounds 1, 2, 6, 10, and 14 displayed potent in vivo anti-inflammatory efficacy with inhibition of NO production in a dose-dependent manner.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Streptomyces Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Streptomyces Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article