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Natural Product Research
Formerly Natural Product Letters
Volume 34, 2020 - Issue 3
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Research Articles

Fupyrones A and B, two new α-pyrones from an endophytic fungus, Fusarium sp. F20

Han GaoDepartment of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University, Qingdao, People’s Republic of China; View further author information
,
Gang LiDepartment of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University, Qingdao, People’s Republic of China; ORCID Iconhttp://orcid.org/0000-0003-0621-2779View further author information
ORCID Icon,
Xiao-Ping PengDepartment of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University, Qingdao, People’s Republic of China; View further author information
&
Hong-Xiang LouDepartment of Natural Medicinal Chemistry and Pharmacognosy, School of Pharmacy, Qingdao University, Qingdao, People’s Republic of China; ;Department of Natural Product Chemistry, Key Laboratory of Chemical Biology of Ministry of Education, School of Pharmaceutical Sciences, Shandong University, Jinan, People’s Republic of ChinaCorrespondence[email protected]
View further author information
Pages 335-340 | Received 27 Jul 2018, Accepted 30 Sep 2018, Published online: 03 Jan 2019

References

  • Bhat ZS, Rather MA, Maqbool M, Lah HU, Yousuf SK, Ahmad Z. 2017. α-Pyrones: small molecules with versatile structural diversity reflected in multiple pharmacological activities-an update. Biomed Pharmacother. 91:265–277.
  • Bode HB, Bethe B, Höfs R, Zeeck A. 2002. Big effects from small changes: possible ways to explore nature’ chemical diversity. ChemBiochem. 3(7):619–627.
  • Cai R, Chen S, Liu Z, Tan C, Huang X, She Z. 2017. A new α-pyrone from the mangrove endophytic fungus Phomopsis sp. HNY29-2B. Nat Prod Res. 31(2):124–130.
  • Fu P, Liu PP, Gong QH, Wang Y, Wang P, Zhu WM. 2013. α-Pyrones from the marine-derived actinomycete Nocardiopsis dassonvillei subsp dassonvillei XG-8-1. ‘Rsc’ Adv. 3(43):20726–20731.
  • Gao H, Li G, Lou HX. 2018. Structural diversity and biological activities of novel secondary metabolites from endophytes. Molecules. 23(3):646–676.
  • Kusari S, Hertweck C, Spiteller M. 2012. Chemical ecology of endophytic fungi: origins of secondary metabolites. Chem Biol. 19(7):792–798.
  • Kusari S, Lamshoft M, Zuhlke S, Spiteller M. 2008. An endophytic fungus from Hypericum perforatum that produces hypericin. J Nat Prod. 71(2):159–162.
  • Li G, Kusari S, Golz C, Strohmann C, Spiteller M. 2016. Three cyclic pentapeptides and a cyclic lipopeptide produced by endophytic Fusarium decemcellulare LG53. RSC Adv. 6(59):54092–54098.
  • Li G, Kusari S, Kusari P, Kayser O, Spiteller M. 2015. Endophytic Diaporthe sp. LG23 produces a potent antibacterial tetracyclic triterpenoid. J Nat Prod. 78(8):2128–2132.
  • Li G, Kusari S, Lamshoft M, Schuffler A, Laatsch H, Spiteller M. 2014. Antibacterial secondary metabolites from an endophytic fungus, Eupenicillium sp. LG41. J Nat Prod. 77(11):2335–2341.
  • Li G, Lou HX. 2018. Strategies to diversify natural products for drug discovery. Med Res Rev. 38(4):1255–1294.
  • Niu C-S, Li Y, Liu Y-B, Ma S-G, Liu F, Li L, Xu S, Wang X-J, Wang R-B, Qu J, Yu S-S. 2017. Pierisketolide A and pierisketones B and C, three diterpenes with an unusual carbon skeleton from the roots of Pieris formosa. Org Lett. 19(4):906–909.
  • Sang X-N, Chen S-F, Tang M-X, Wang H-F, An X, Lu X-J, Zhao D, Wang Y-B, Bai J, Hua H-M, et al. 2017. α-Pyrone derivatives with cytotoxic activities, from the endophytic fungus Phoma sp. YN02-P-3. Bioorg Med Chem Lett. 27(16):3723–3725.
  • Schaberle TF. 2016. Biosynthesis of α-pyrones. Beilstein J Org Chem. 12:571–588.
  • Yadav JS, Ganganna B, Dutta P, Singarapu KK. 2014. Synthesis and determination of absolute configuration of α-pyrones isolated from Penicillium corylophilum. J Org Chem. 79(22):10762–10771.
  • Ying YM, Zhang LW, Shan WG, Zhan ZJ. 2014. Secondary metabolites of Peyronellaea sp. XW-12, an endophytic fungus of Huperzia serrata. Chem Nat Compd. 50(4):723–725.
  • Zhang J, Jiang Y, Cao Y, Liu J, Zheng D, Chen X, Han L, Jiang C, Huang X. 2013. Violapyrones A-G, α-pyrone derivatives from Streptomyces violascens isolated from Hylobates hoolock feces. J Nat Prod. 76(11):2126–2130.
  • Zhang XM, Sun MW, Shi H, Lu CH. 2017. α-Pyrone derivatives from a marine actinomycete Nocardiopsis sp. YIM M13066. Nat Prod Res. 31(19):2245–2249.
  • Zhao T, Chang Y, Zhu T, Li J, Gu Q, Li D, Che Q, Zhang G. 2018. Pyrone derivatives with cyto-protective activity from two Takla Makan desert soil derived actinomycete Nocardiopsis strains recovered in seawater based medium. Nat Prod Res. 1–9. α
  • Zhou J, Liu J, Dang T, Zhou H, Zhang H, Yao G. 2018. Mollebenzylanols A and B, highly modified and functionalized diterpenoids with a 9-benzyl-8,10-dioxatricyclo[5.2.1.01,5]decane core from Rhododendron molle. Org Lett. 20(7):2063–2066.

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