| Literature DB >> 25469855 |
Chia-Ching Liaw1, Hui-Chi Huang2, Ping-Chun Hsiao3, Li-Jie Zhang3, Zhi-Hu Lin3, Syh-Yuan Hwang4, Feng-Lin Hsu5, Yao-Haur Kuo3.
Abstract
Five new 5β,19-epoxycucurbitane triterpenoids, taikugausins A-E (1-5), together with 5β,19-epoxy-25-methoxycucurbita-6,23-diene-3β,19-diol (6), have been isolated and characterized from the 70 % EtOH extract of the fresh fruits of Momordica charantia. The chemical structures of compounds 1-6 were elucidated on the basis of extensive spectroscopic analyses, especially 2D NMR (HMQC, HMBC, and NOESY) experiments and HRESIMS data. The relationship between NMR chemical shifts and the configuration of C-19 with an OMe group in 5β,19-epoxycucurbitane are described. Among them, compounds 3 and 4 exhibited remarkable anti-inflammatory activities by the inhibition of nitric oxide production at the concentration of 10 µg/mL. In addition, 3 and 4 also showed moderate cytotoxicity against WiDr, Hep G2, MCF-7, and HEp-2 human tumor cell lines. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2014 PMID: 25469855 DOI: 10.1055/s-0034-1383307
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352