| Literature DB >> 23098899 |
Jian-Yong Dong1, Xi-Yan Ma, Xiao-Qin Cai, Peng-Cheng Yan, Lei Yue, Chen Lin, Wei-Wei Shao.
Abstract
Five sesquiterpenoids, 1α,8α-epidioxy-4α-hydroxy- 5αH-guai-7(11),9-dien- 12,8-olide. (1), 8,9-seco-4β-hydroxy-1α,5βH-7(11)-guaen-8,10-olide (2), 8α-hydroxy-1α, 4β,7βH-guai-10(15)-en- 5β,8β-endoxide(3), 7β,8α-dihydroxy-1α,4αH-guai-10(15)-en-5β,8β-endoxide(4) and 7-hydroxy-5(10),6,8-cadinatriene-4-one(5), together with seven known analogs were isolated from the rhizomes of Curcuma wenyujin. Their structures and relative configurations were determined on the basis of spectroscopic methods including 2D NMR techniques, and the structures of 1 and 2 were confirmed by single-crystal X-ray diffraction experiment. Compounds 1-10 and 12 showed significant in vitro antiviral activity against the influenza virus A with IC₅₀ values ranged from 6.80 to 39.97 μM, and SI values ranged from 6.35 to 37.25.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23098899 DOI: 10.1016/j.phytochem.2012.09.008
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072