| Literature DB >> 27575477 |
Nwet Nwet Win1, Takuya Ito2, Yi Yi Win3, Hla Ngwe3, Takeshi Kodama2, Ikuro Abe4, Hiroyuki Morita5.
Abstract
Viral protein R (Vpr) is an accessory protein that plays important roles in the viral pathogenesis of Human Immunodeficiency Virus-1 (HIV-1). An assay for anti-Vpr activity, using TREx-HeLa-Vpr cells, is a promising strategy to discover Vpr inhibitors. The anti-Vpr assay revealed that the CHCl3-soluble extract of Picrasma javanica bark possesses potent anti-Vpr activity. Furthermore, studies of quassinoids (1-15) previously isolated from the extract demonstrated that all of the tested quassinoids exhibit anti-Vpr activity. Among the tested compounds, javanicin I (15) exhibited the most potent anti-Vpr activity ((***)p <0.001) in comparing with that of the positive control, damnacanthal. The structure-activity relationships of the active quassinoids suggested that the presence of a methyl group at C-13 in the 2,12,14-triene-1,11,16-trione-2,12-dimethoxy-18-norpicrasane quassinoids is the important factor for the potent inhibitory effect in TREx-HeLa-Vpr cells.Entities:
Keywords: Picrajavanicins; Picrasma javanica; Quassinoids; Structure–activity relationships; Viral protein R inhibitors
Mesh:
Substances:
Year: 2016 PMID: 27575477 DOI: 10.1016/j.bmcl.2016.08.055
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823