4.7 Article

Anti-HIV Tigliane Diterpenoids from Wikstroemia scytophylla

期刊

JOURNAL OF NATURAL PRODUCTS
卷 83, 期 12, 页码 3584-3590

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.0c00700

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资金

  1. Japan Society for the Promotion of Science KAKENHI [17K08348, 26460133]
  2. U.S.-Japan Cooperative Medical Sciences Program Collaborative Awards from AMED [18950036]
  3. NIAID [64061]
  4. National Natural Science Foundation of China [81673323]
  5. Liaoning Revitalization Talents Program [XLYC1807118]
  6. NIH [AI33066-27]
  7. Grants-in-Aid for Scientific Research [17K08348, 26460133] Funding Source: KAKEN

向作者/读者索取更多资源

During a chemical investigation of Wikstroemia scytophylla, three new [wikstrocins A-C (1-3)] and three known tigliane diterpenoids (4-6) were isolated. The structures of the new compounds were elucidated from extensive physiochemical and spectroscopic analysis. The correlations between the ECD Cotton effects and B ring structures of tiglianes were also evaluated. The isolated compounds were assessed for their anti-HIV activity against HIV-1 infection of MT4 cells, and two compounds (4 and 6) showed potent anti-HIV activity with IC50 values of 3.8 and 12.8 nM, respectively.

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