| Literature DB >> 26696523 |
Chen Zhang1, Shu Wang2, Ke-Wu Zeng1, Jun Li3, Daneel Ferreira4, Jordan K Zjawiony4, Bing-Yu Liu1, Xiao-Yu Guo1, Hong-Wei Jin1, Yong Jiang1, Peng-Fei Tu1.
Abstract
Twelve new dimeric sesquiterpenoids (1-12) were isolated from the dried whole plants of Artemisia rupestris. Their structures were determined using MS and NMR data, and the absolute configurations were elucidated on the basis of experimental and calculated ECD spectra. Compounds 1-9 are presumably formed via biocatalyzed [2+2] or [4+2] cycloaddition reactions. Stereoselectivity of the [4+2] Diels-Alder reaction dictated the formation of endo-products. The dimeric sesquiterpenoids exhibited moderate inhibition on NO production stimulated by lipopolysaccharide in BV-2 microglial cells, with IC50 values in the range 17.0-71.8 μM.Entities:
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Year: 2015 PMID: 26696523 DOI: 10.1021/acs.jnatprod.5b00894
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050