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Discovery of olimycin E from Streptomyces sp. 11695.
Tu, Lirong; Shen, Shumei; Yan, Zhenyang; Li, Xiaoxia; Liu, Kai; Xu, Jin; Luo, Minghe.
Afiliación
  • Tu L; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
  • Shen S; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
  • Yan Z; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
  • Li X; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
  • Liu K; Guangxi Key Laboratory of Marine Drugs/Institute of Marine Drugs, Guangxi University of Chinese Medicine, Nanning, People's Republic of China.
  • Xu J; Chongqing College of Traditional Chinese Medicine, Chongqing, People's Republic of China.
  • Luo M; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, People's Republic of China.
Nat Prod Res ; : 1-6, 2024 Apr 08.
Article en En | MEDLINE | ID: mdl-38586959
ABSTRACT
A new natural product olimycin E (1), together with two known compounds of divergolide R (2) and olimycin B (3), were obtained from the marine-derived Streptomyces sp. 11695. The structures of 1-3 were established on the basis of HRESIMS as well as 1D and 2D NMR datasets. The absolute configuration of 1 is identified as 4 R, 6S, 7S, 10 R by comparison the experiment ECD with that of the theoretical ECD. Antibacterial results showed that compound 2 have antibacterial activities against Staphylococcus aureus and MRSA with the MIC values of 32 µg/mL, respectively.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article
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