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Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1.
Ning, Yaodong; Zhang, Shi; Zheng, Te; Xu, Yao; Li, Song; Zhang, Jianpeng; Jiao, Binghua; Zhang, Yun; Ma, Zengling; Lu, Xiaoling.
  • Ning Y; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
  • Zhang S; College of Life and Environmental Sciences, Wenzhou University, Wenzhou 325000, China.
  • Zheng T; Biology Institute, Qilu University of Technology, Shandong Academy of Sciences, Jinan 250000, China.
  • Xu Y; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
  • Li S; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
  • Zhang J; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
  • Jiao B; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
  • Zhang Y; Biology Institute, Qilu University of Technology, Shandong Academy of Sciences, Jinan 250000, China.
  • Ma Z; College of Life and Environmental Sciences, Wenzhou University, Wenzhou 325000, China.
  • Lu X; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai 200433, China.
Mar Drugs ; 21(10)2023 Oct 18.
Article en En | MEDLINE | ID: mdl-37888476
ABSTRACT
The Arctic-derived fungus Eutypella sp. D-1 can produce numerous secondary metabolites, and some compounds exhibit excellent biological activity. Seven pimarane-type diterpenes, including three new compounds eutypellenone F (1), libertellenone Y (2), and libertellenone Z (3), and four known compounds (4-7), were isolated from fermentation broth of Eutypella sp. D-1 by the OSMAC strategy of adding ethanol as a promoter in the culture medium. Compound 2 has a rare tetrahydrofuran-fused pimarane diterpene skeleton. The anti-inflammatory activity of all compounds was evaluated. Compounds 3-6 showed a significant inhibitory effect on cell NO release at 10 µmol/L by in vitro experiments, of which 3-5 had inhibitory rates over 60% on nitric oxide (NO) release. Subsequently, the anti-inflammatory activity of 3-5 was evaluated based on a zebrafish model, and the results showed that 3 had a significant inhibitory effect on inflammatory cells migration at 40 µmol/L, while 4 and 5 had a significant inhibitory effect at 20 µmol/L. Moreover, compounds 3-5 have the same conjugated double bond structure, which may be an important group for these compounds to exert anti-inflammatory activity.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Xylariales / Diterpenos Límite: Animals Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Xylariales / Diterpenos Límite: Animals Idioma: En Año: 2023 Tipo del documento: Article