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Eutypellenoids A⁻C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1.
Yu, Hao-Bing; Wang, Xiao-Li; Xu, Wei-Heng; Zhang, Yi-Xin; Qian, Yi-Sen; Zhang, Jian-Peng; Lu, Xiao-Ling; Liu, Xiao-Yu.
Afiliación
  • Yu HB; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, and Marine Biopharmaceutical Institute, Second Military Medical University, Shanghai 200433, China. yuhaobing1986@126.com.
  • Wang XL; Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California, San Diego, CA 92093, USA. yuhaobing1986@126.com.
  • Xu WH; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, and Marine Biopharmaceutical Institute, Second Military Medical University, Shanghai 200433, China. xlwang0417@163.com.
  • Zhang YX; School of Pharmacy, Second Military Medical University, Shanghai 200433, China. xuweiheng7114@163.com.
  • Qian YS; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, and Marine Biopharmaceutical Institute, Second Military Medical University, Shanghai 200433, China. smmu_zyx@163.com.
  • Zhang JP; School of Physical Sciences, University of California, Irvine, CA 92697, USA. yisenq1@uci.edu.
  • Lu XL; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, and Marine Biopharmaceutical Institute, Second Military Medical University, Shanghai 200433, China. zjp80072002@hotmail.com.
  • Liu XY; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, and Marine Biopharmaceutical Institute, Second Military Medical University, Shanghai 200433, China. luxiaoling80@126.com.
Mar Drugs ; 16(8)2018 Aug 16.
Article en En | MEDLINE | ID: mdl-30115869
ABSTRACT
Three new pimarane diterpenes, eutypellenoids A⁻C (1⁻3), together with a known compound, eutypenoid C (4), were isolated from the culture extract of Eutypella sp. D-1 derived from the Arctic region. Compounds 1⁻3 possessed an uncommon tetrahydrofuran-fused pimarane diterpene skeleton. The structures of all compounds were determined by detailed spectroscopic analysis, electronic circular dichroism (ECD) analysis, as well as a comparison with the literature data. Antibacterial, antifungal, and cytotoxic activities of these compounds were evaluated. Compound 2 displayed antibacterial activity against Staphylococcus aureus and Escherichia coli with MIC values of 8 and 8 µg/mL, respectively. Additionally, compound 2 showed antifungal activity against Candidaparapsilosis, Candida albicans, Candida glabrata, and Candida tropicalis with MIC values of 8, 8, 16, and 32 µg/mL, respectively. Furthermore, compound 2 exhibited moderate cytotoxic activity against HCT-116 cell line with IC50 value of 3.7 µM.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Xylariales / Abietanos / Diterpenos Límite: Humans Idioma: En Revista: Mar Drugs Asunto de la revista: BIOLOGIA / FARMACOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Xylariales / Abietanos / Diterpenos Límite: Humans Idioma: En Revista: Mar Drugs Asunto de la revista: BIOLOGIA / FARMACOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: China