4.5 Article

Quassinoids: Viral protein R inhibitors from Picrasma javanica bark collected in Myanmar for HIV infection

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 26, 期 19, 页码 4620-4624

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2016.08.055

关键词

Viral protein R inhibitors; Quassinoids; Picrajavanicins; Picrasma javanica; Structure-activity relationships

资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. Japan Society for the Promotion of Science
  3. Kobayashi International Scholarship Foundation
  4. Tokyo Biochemical Research Foundation [TBRF-RF-14-84]
  5. Grants-in-Aid for Scientific Research [26460140, 15H05138] Funding Source: KAKEN

向作者/读者索取更多资源

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-triene1,11,16-trione-2,12-dimethoxy-18-norpicrasane quassinoids is the important factor for the potent inhibitory effect in TREx-HeLa-Vpr cells. (C) 2016 Elsevier Ltd. All rights reserved.

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