Your browser doesn't support javascript.
loading
Tigliane Diterpenoids with Larvicidal, Antifungal, and α-Glucosidase Inhibitory Activities from Croton damayeshu.
Jiang, Zhi-Yong; Feng, Jin-E; Duan, Li-Kun; Liu, Chun-Jiang; Li, Xiao-Fei; Huang, Chun-Qiu; Shi, Sheng-Li; Wang, Rui-Rui; Zuo, Ai-Xue; He, Hong-Ping.
Afiliação
  • Jiang ZY; School of Ethnic Medicine, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, People's Republic of China.
  • Feng JE; Key Laboratory of Modern Research on Ethnic Medicine in Colleges of Yunnan Province, Kunming 650500, Yunnan, People's Republic of China.
  • Duan LK; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650500, Yunnan, People's Republic of China.
  • Liu CJ; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650500, Yunnan, People's Republic of China.
  • Li XF; School of Ethnic Medicine, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, People's Republic of China.
  • Huang CQ; School of Ethnic Medicine, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, People's Republic of China.
  • Shi SL; Yunnan Phytopharmaceutical Co. Ltd., Kunming 650505, Yunnan, People's Republic of China.
  • Wang RR; College of Chemical Biology & Enviromeny, Yuxi Normal University, Yuxi 653100, Yunnan, People's Republic of China.
  • Zuo AX; School of Ethnic Medicine, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, People's Republic of China.
  • He HP; School of Ethnic Medicine, Yunnan University of Chinese Medicine, Kunming 650500, Yunnan, People's Republic of China.
J Nat Prod ; 85(2): 405-414, 2022 02 25.
Article em En | MEDLINE | ID: mdl-35080403
ABSTRACT
Thirty-five tigliane diterpenoids and two ent-kaurane diterpenoids were isolated from the leaves of Croton damayeshu, and, among them, compounds 1-10 were characterized as new tigliane diterpenoids. The structures of compounds 1-10 were determined by analysis of their HRESIMS, NMR, and ECD data and by chemical methods. The isolates were assayed for their larvicidal, antifungal, and α-glucosidase inhibitory activities, and compounds 8-10 were found to possess larvicidal activities against Plutella xylostella with LC50 values of 0.19, 0.16, and 0.26 µM, respectively, comparable to the LC50 of 0.14 µM for the positive control, flubendiamide.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Forbóis / Croton / Diterpenos do Tipo Caurano / Diterpenos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Forbóis / Croton / Diterpenos do Tipo Caurano / Diterpenos Idioma: En Ano de publicação: 2022 Tipo de documento: Article