| Literature DB >> 25800107 |
Hucheng Zhu1, Chunmei Chen1, Junjun Liu1, Bin Sun1, Guangzheng Wei1, Yan Li2, Jinwen Zhang3, Guangmin Yao1, Zengwei Luo1, Yongbo Xue4, Yonghui Zhang5.
Abstract
Eight polyprenylated spirocyclic acylphloroglucinol derivatives (PSAPs), hyperascyrones A-H, were isolated from the aerial parts of Hypericum ascyron Linn., together with six known analogs. Their structures were established by spectroscopic analyses including HRESIMS, 1D and 2D NMR, and their absolute configurations were determined by electronic circular dichroism calculations (ECD, Gaussian 09). Structures of previously reported tomoeones C, D, G, and H were revised. Hyperascyrones A-H were evaluated for their cytotoxic and anti-HIV-1 activities, with hyperascyrones C and G exhibiting significant cytotoxicities against HL-60 cell lines with IC50 values of 4.22 and 8.36 μM, respectively. In addition, the chemotaxonomic significance of these compounds was also discussed.Entities:
Keywords: Anti-HIV-1 activities; Cytotoxic activities; Hypericaceae; Hypericum ascyron Linn.; Polycyclic polyprenylated acylphloroglucinols; Polyprenylated spirocyclic acylphloroglucinol derivatives
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Year: 2015 PMID: 25800107 DOI: 10.1016/j.phytochem.2015.02.009
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072