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New α-pyrones from an endophytic fungus, Hypoxylon investiens J2.
Yuan, Chao; Yang, Hong-Xia; Guo, Yu-Hua; Fan, Lin; Zhang, Ying-Bo; Li, Gang.
Afiliação
  • Yuan C; Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Sciences CATAS Haikou 571101 People's Republic of China.
  • Yang HX; Department of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University Qingdao 266021 People's Republic of China gang.li@qdu.edu.cn +86-532-8299-1172.
  • Guo YH; Shandong Drug and Food Vocational College Weihai Shandong 264210 People's Republic of China.
  • Fan L; Weihai Vocational College Weihai 264210 People's Republic of China.
  • Zhang YB; Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Sciences CATAS Haikou 571101 People's Republic of China.
  • Li G; Department of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University Qingdao 266021 People's Republic of China gang.li@qdu.edu.cn +86-532-8299-1172.
RSC Adv ; 9(47): 27419-27423, 2019 Aug 29.
Article em En | MEDLINE | ID: mdl-35529215
ABSTRACT
Four new α-pyrones, hypotiens A-D (1-4), were isolated from a fungal endophyte, Hypoxylon investiens J2, harbored in the medicinal plant Blumea balsamifera. Their structures were determined through detailed HRMS and NMR spectroscopic data. Compounds 1-4 are new α-pyrone derivatives containing an unusual dimethyl substitution in the highly unsaturated side chain. Their plausible biosynthetic pathway was discussed. Biological assay indicated that compounds 1-4 showed no antimicrobial, quorum sensing inhibitory, and cytotoxic activities. The specific side chain in α-pyrone derivatives 1-4 might be responsible for the weak pharmacological activities.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article