Literature DB >> 25800107

Hyperascyrones A-H, polyprenylated spirocyclic acylphloroglucinol derivatives from Hypericum ascyron Linn.

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.
Copyright © 2015 Elsevier Ltd. All rights reserved.

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


  5 in total

Review 1.  Characteristic metabolites of Hypericum plants: their chemical structures and biological activities.

Authors:  Naonobu Tanaka; Yoshiki Kashiwada
Journal:  J Nat Med       Date:  2021-02-08       Impact factor: 2.343

2.  Hyperpatulones A-F, polycyclic polyprenylated acylphloroglucinols from Hypericum patulum and their cytotoxic activities.

Authors:  Zhong-Nan Wu; Qian-Wen Niu; Yu-Bo Zhang; Ding Luo; Qing-Guo Li; Ying-Ying Li; Guang-Kai Kuang; Li-Jun He; Guo-Cai Wang; Yao-Lan Li
Journal:  RSC Adv       Date:  2019-03-12       Impact factor: 4.036

3.  (±)-Japonones A and B, two pairs of new enantiomers with anti-KSHV activities from Hypericum japonicum.

Authors:  Linzhen Hu; Hucheng Zhu; Lei Li; Jinfeng Huang; Weiguang Sun; Junjun Liu; Hua Li; Zengwei Luo; Jianping Wang; Yongbo Xue; Yu Zhang; Yonghui Zhang
Journal:  Sci Rep       Date:  2016-06-08       Impact factor: 4.379

4.  Hyperjaponol H, A New Bioactive Filicinic Acid-Based Meroterpenoid from Hypericum japonicum Thunb. ex Murray.

Authors:  Rongrong Wu; Zijun Le; Zhenzhen Wang; Shuying Tian; Yongbo Xue; Yong Chen; Linzhen Hu; Yonghui Zhang
Journal:  Molecules       Date:  2018-03-18       Impact factor: 4.411

5.  Hyperisampsins H-M, Cytotoxic Polycyclic Polyprenylated Acylphloroglucinols from Hypericum sampsonii.

Authors:  Hucheng Zhu; Chunmei Chen; Qingyi Tong; Xintao Chen; Jing Yang; Junjun Liu; Bin Sun; Jianping Wang; Guangmin Yao; Zengwei Luo; Yongbo Xue; Yonghui Zhang
Journal:  Sci Rep       Date:  2015-10-06       Impact factor: 4.379

  5 in total

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