Fusaresters A–E, new γ-pyrone-containing polyketides from fungus Fusarium sp. Hungcl and structure revision of fusariumin D. Issue 22 (1st May 2019)

• Record Type: Journal Article
• Authors: Gong, Jiaojiao; Chen, Chunmei; Mo, Shuyuan; Liu, Junjun; Wang, Wenjing; Zang, Yi; Li, Huaqiang; Chai, Chenwei; Zhu, Hucheng; Hu, Zhengxi; Wang, Jianping; Zhang, Yonghui
• Is Part Of: Organic & biomolecular chemistry. Volume 17:Issue 22(2019)
• Page Start: 5526
• Page End: 5532
• Publication Date: 2019-05-01
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c9ob00534j
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : Chemical investigation of a marine-derived fungus Fusarium sp. Hungcl afforded five new γ-pyrone-containing polyketides, fusaresters A–E. Abstract : Marine-derived fungi have been regarded as an under-explored and promising reservoir of structurally novel and bioactive natural products. In this study, five new γ-pyrone-containing polyketides, fusaresters A–E (1–5 ), were isolated and identified from the culture extracts of a marine-derived fungus Fusarium sp. Hungcl. The structures of compounds1–5 were elucidated on the basis of their HRESIMS and NMR spectroscopic data as well as 13 C NMR calculation and electronic circular dichroism (ECD) analyses. Remarkably, the structure of fusariumin D was revised to (9 S *, 11 S *)-3 . All these isolates were tested for the cytotoxicity against seven human cancer cell lines, including SW480, HL-60, A549, MCF-7, HepG2, HeLa and SMMC-7721, and the inhibitory activity against protein tyrosine phosphatase 1B (PTP1B). The results revealed that only compound2 showed a weak inhibition rate of 56% at 40 μM.