| Literature DB >> 27934392 |
Lei Li1,2, Huan Li2,3, Xing-Rong Peng1, Bo Hou1,2, Mu-Yuan Yu1,2, Jin-Run Dong1,2, Xiao-Nian Li1, Lin Zhou1, Jian Yang3, Ming-Hua Qiu1,2.
Abstract
(±)-Ganoapplanin (1), a pair of novel meroterpenoid enantiomers featuring an unprecedented dioxaspirocyclic skeleton constructed from a 6/6/6/6 tetracyclic system and an unusual tricyclo[4.3.3.03',7']dodecane motif, were isolated from Ganoderma applanatum. Its structure and absolute configurations were determined by spectroscopic analyses, X-ray crystallography, and ECD (electronic circular dichroism calculations). A plausible biogenetic pathway, involving a key Gomberg-Bachmann reaction, was also proposed for (±)-1. Biological studies showed that (±)-1 and its enantiomers exhibited different inhibitory activities on T-type voltage-gated calcium channels.Entities:
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Year: 2016 PMID: 27934392 DOI: 10.1021/acs.orglett.6b03064
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005