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Cyclic peroxides and analogs: Antibacterial, antimalarial, and cytotoxic marine products from Xisha sponge Diacarnus sp.
Leng, Xue; He, Hongying; Lazaro, J Enrico H; Chen, Xiaohui; Ouyang, Han; Li, Te; Yan, Xia; He, Shan.
Afiliação
  • Leng X; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo, 315211, Zhejiang, China.
  • He H; School of Pharmaceutical Sciences, Xiamen University, Xiamen, 361102, Fujian, China.
  • Lazaro JEH; National Institute of Molecular Biology and Biotechnology, University of the Philippines Diliman, Quezon, 1101, Philippines.
  • Chen X; School of Pharmaceutical Sciences, Xiamen University, Xiamen, 361102, Fujian, China.
  • Ouyang H; Institute of Drug Discovery Technology, Ningbo University, Ningbo, 315211, Zhejiang, China.
  • Li T; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo, 315211, Zhejiang, China.
  • Yan X; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo, 315211, Zhejiang, China. Electronic address: yanxia@nbu.edu.cn.
  • He S; Li Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Health Science Center, Ningbo University, Ningbo, 315211, Zhejiang, China; State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, China. Electronic address: heshan@nbu.edu.cn.
Phytochemistry ; 223: 114097, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38641142
ABSTRACT
A chemical investigation of the dichloromethane extract from the Xisha sponge Diacarnus sp. revealed seven undescribed norterpene cyclic peroxides, named diacarperoxides T-Z, and five unreported related norterpenes, named diacarnoids E-I, and eleven previously reported compounds. The structures of these isolated compounds, including their absolute configurations, were elucidated based on extensive spectroscopic analyses, electronic circular dichroism (ECD) calculations, Snatzke's method, [Rh2(OCOCF3)4]-induced ECD spectra, and modified Mosher's method. Bioassays were performed to assess the antibacterial activity against six pathogenic bacteria, cytotoxicities toward three cancer cell lines, and antimalarial activity against Plasmodium parasites. Most of the cyclic peroxides exhibited substantial antibacterial activity (MIC 1-8 µg/mL). Diacarperoxide W and nuapapuin A showed substantial antimalarial activity with IC50 values of 0.98 and 2.83 µM. Moreover, many compounds exhibited <50% cell survival rates, and IC50 values of 0.22-6.33 µM. The apoptosis assay showed that nuapapuin A induced cancer cell apoptosis in a dose-dependent manner.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peróxidos / Poríferos / Antibacterianos / Antimaláricos Limite: Animals / Humans Idioma: En Revista: Phytochemistry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peróxidos / Poríferos / Antibacterianos / Antimaláricos Limite: Animals / Humans Idioma: En Revista: Phytochemistry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido