| Literature DB >> 25647077 |
Taizong Wu1, Qian Wang2, Cheng Jiang1, Susan L Morris-Natschke3, Hui Cui1, Yan Wang2, Yuan Yan2,4, Jun Xu1, Kuo-Hsiung Lee3,5, Qiong Gu1,3.
Abstract
Bioassay-guided fractionation was conducted on an EtOAc-soluble extract of the whole plants of Scutellaria barbata, monitored by inhibition of Epstein-Barr virus (EBV) lytic replication. Twenty-six neo-clerodane diterpenoids were isolated, of which 13 are new (1-13, scutolides A-L) and 13 previously known (14-26). The structures of 1-13 were elucidated by analysis of their NMR and MS spectroscopic data. Furthermore, the configurations of the new compounds 1 and 11 were confirmed by single-crystal X-ray diffraction. All of the isolated compounds were evaluated for inhibitory effects against EBV lytic replication. Eleven compounds (3, 4, 6, 11, 12, 15, 16, 17, 20, 22, and 24) exhibited moderate to potent inhibition, with EC50 values from 3.2 to 23.6 μM and selective index (SI) values from 2.1 to 109.2. More specifically, the new compound 4 showed the most potent activity, with EC50 and SI values of 3.2 μM and 46.1, respectively, while compound 24 (EC50 = 16.4 μM) exhibited the highest SI of 109.2. This study is the first to report that neo-clerodane diterpenoids demonstrate significant inhibition against EBV lytic replication.Entities:
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Year: 2015 PMID: 25647077 DOI: 10.1021/np500988m
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050