1. Four New Picrotoxane-Type Sesquiterpenes From Dendrobium nobile Lindl
- Author
-
Jing-Zhe Yuan, Sheng-Zhuo Huang, Hao Wang, Guoliang Zhu, Cai-Hong Cai, Xing-Lian Xu, Xin Chen, Wen-Li Mei, Hao-Fu Dai, and Pei Wang
- Subjects
Formamide ,picrotoxane ,Stereochemistry ,Carbon skeleton ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Dendrobium nobile ,HeLa ,lcsh:Chemistry ,chemistry.chemical_compound ,sesquiterpenes ,Bond cleavage ,chemistry.chemical_classification ,α-glycosidase inhibitor ,biology ,General Chemistry ,Dendrobium nobile Lindl ,021001 nanoscience & nanotechnology ,biology.organism_classification ,0104 chemical sciences ,chemistry ,lcsh:QD1-999 ,cytotoxicity ,0210 nano-technology ,Lactone - Abstract
Four picrotoxane-type sesquiterpenes, dendroterpene A-D (1-4), together with four known compounds (5-8), were isolated from the stems of Dendrobium nobile Lindl. Their structures were elucidated by spectroscopic analysis, X-ray diffraction analysis, analysis of the ECD data according to the Klyne's lactone sector rule, and quantum ECD calculation. Compounds 1 and 2 are two new picrotoxane-type sesquiterpenes with a new carbon skeleton containing a formamide group, which may be derived from the previously reported dendrobiumane B skeleton by the C(9)-C(11) carbon bond cleavage. Compounds 3, 5, 6, and 8 exhibited inhibitory activity against α-glycosidase. Compounds 5 and 6 were cytotoxic against SGC-7901, K562, A549, BEL-7402, and Hela cell lines.
- Published
- 2019