| Literature DB >> 31556297 |
Jiabao Liu1, Pankaj Pandey, Xiaojuan Wang2, Kamesha Adams, Xinzhu Qi1, Jiabao Chen1, Hua Sun1, Qi Hou1, Daneel Ferreira, Robert J Doerksen, Mark T Hamann2, Shuai Li1.
Abstract
Three new tetrahydrobenzocyclooctabenzofuranone lignan glucosides, longipedunculatins A-C (1-3), a new dibenzocyclooctadiene lignan glucoside, longipedunculatin D (4), a new dibenzocyclooctadiene lignan (5), five new tetrahydrobenzocyclooctabenzofuranone lignans (6-10), and two new simple lignans (11, 12) were isolated from the roots of Kadsura longipedunculata. Their structures and absolute configurations were established using a combination of MS, NMR, and experimental and calculated electronic circular dichroism data. Compound 7 showed moderate hepatoprotective activity against N-acetyl-p-aminophenol-induced toxicity in HepG2 cells with a cell survival rate at 10 μM of 50.8%. Compounds 2, 7, and 12 showed significant in vitro inhibitory effects with an inhibition rate of 55.1%, 74.9%, and 89.8% on nitric oxide production assays at 10 μM.Entities:
Year: 2019 PMID: 31556297 DOI: 10.1021/acs.jnatprod.9b00576
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050