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Natural Product Research
Formerly Natural Product Letters
Volume 35, 2021 - Issue 23
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Research Articles

Ustusaustin A: a new neuraminidase inhibitory meroterpene from the ascidian-derived endophytic fungus Aspergillus ustus TK-5

Xin Lia Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China;b Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China;ORCID Iconhttps://orcid.org/0000-0001-5622-7333View further author information
ORCID Icon,
Li Lia Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China;c College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, Beijing, ChinaView further author information
,
Xiao-Ming Lia Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China;b Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China;View further author information
,
Hong-Lei Lia Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China;b Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China;View further author information
,
Belma Konuklugild Department of Pharmacognosy, Faculty of Pharmacy, Ankara University, Ankara, TurkeyView further author information
&
Bin-Gui Wanga Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China;b Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China;;e Center for Ocean Mega-Science, Chinese Academy of Sciences, Qingdao, ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0003-0116-6195View further author information
ORCID Icon
Pages 4939-4944 | Received 24 Feb 2020, Accepted 29 Mar 2020, Published online: 14 Apr 2020

References

  • Bang S, Li W, Ha TKQ, Lee C, Oh WK, Shim SH. 2018. Anti-influenza effect of the major flavonoids from Salvia plebeia R.Br. via inhibition of influenza H1N1 virus neuraminidase. Nat Prod Res. 32(10):1224–1228.
  • Cao Y, Zang Y, Huang X, Cheng Z. 2019. Chemical constituents from Artemisia rupestris and their neuraminidase inhibitory activity. Nat Prod Res. 1–8. DOI:10.1080/14786419.2019.1639178.
  • Chexal KK, Springer JP, Clardy J, Cole RJ, Kirksey JW, Dorner JW, Cutler HG, Strawter BJ. 1976. Austin, a novel polyisoprenoid mycotoxin from Aspergillus ustus. J Am Chem Soc. 98(21):6748–6750.
  • Cho J, Yi H, Jang EY, Lee MS, Lee JY, Kang C, Lee CH, Kim K. 2017. Mycophenolic mofetil, an alternative antiviral and immunomodulator for the highly pathogenic avian influenza H5N1 virus infection. Biochem Biophy Res Comm. 494(1–2):298–304.
  • Dao TT, Tung BT, Nguyen PH, Thuong PT, Yoo SS, Kim EH, Kim SK, Oh WK. 2010. C-Methylated flavonoids from Cleistocalyx operculatus and their inhibitory effects on novel influenza A (H1N1) neuraminidase. J Nat Prod. 73(10):1636–1642.
  • Fill TP, Pereira GK, dos Santos RMG, Rodrigues-Fo E. 2007. Four additional meroterpenes produced by Penicillium sp. found in association with Melia azedarach. Possible biosynthetic intermediates to austin. Z Naturforsch. 62(8):1035–1044.
  • Fukuyama K, Katsube Y, Ishido H, Yamazaki M, Maebayashi Y. 1980. The absolute configuration of desacetylaustin isolated from Emericella nidulans var. dentate. Chem Pharm Bull. 28(7):2270–2271.
  • Geris Santos RM, Rodrigues-Filho E. 2003. Structures of meroterpenes produced by Penicillium sp., an endophytic fungus found associated with Melia azedarach. J Braz Chem Soc. 14(5):722–727.
  • Hayashi H, Mukaihara M, Murao S, Arai M, Lee AY, Clardy J. 1994. Acetoxydehydroaustin, a new bioactive compound, and related compound neoaustin from Penicillium sp. MG-ll. Biosci Biotech Biochem. 58(2):334–338.
  • Kannan S, Kolandaivel P. 2017. Antiviral potential of natural compounds against influenza virus hemagglutinin. Comput Biol Chem. 71:207–218.
  • Kim YJ, Ko EJ, Kim MC, Lee YN, Kim KH, Jung YJ, Kang SM. 2017. Roles of antibodies to influenza A virus hemagglutinin, neuraminidase, and M2e in conferring cross protection. Biochem Biophy Res Comm. 493(1):393–398.
  • Kwak HJ, Park S, Kim N, Yoo G, Park JH, Oh Y, Nhiem NX, Kim SH. 2018. Neuraminidase inhibitory activity by compounds isolated from aerial parts of Rhinacanthus nasutus. Nat Prod Res. 32(17):2111–2115.
  • Li XL, Chi LP, Navarro-Vázquez A, Hwang S, Schmieder P, Li XM, Li X, Yang SQ, Lei X, Wang BG, et al. 2020. Stereochemical elucidation of natural products from residual chemical shift anisotropies in a liquid crystalline phase. J Am Chem Soc. 142(5):2301–2309.
  • Li XD, Li X, Li XM, Yin XL, Wang BG. 2019. Antimicrobial bisabolane-type sesquiterpenoids from the deep-sea sediment-derived fungus Aspergillus versicolor SD-330. Nat Prod Res. 1–7. DOI:10.1080/14786419.2019.1696792.
  • Maebayashi Y, Okuyama E, Yamazaki M, Katsube Y. 1982. Structure of ED-1 isolated from Emericella dentate. Chem Pharm Bull. 30(5):1911–1912.
  • Song XY, Qiao LT, Wang JJ, Zeng HM, She ZG, Miao CD, Hong K, Gu YC, Liu L, Lin YC. 2011. Two new meroterpenes from the mangrove endophytic fungus Aspergillus sp. 085241B. HCA. 94(10):1875–1880.
  • Valiante V, Mattern DJ, Schüffler A, Horn F, Walther G, Scherlach K, Petzke L, Dickhaut J, Guthke R, Hertweck C, et al. 2017. Discovery of an extended austinoid biosynthetic pathway in Aspergillus calidoustus. ACS Chem Biol. 12(5):1227–1234.
  • Yang Y, Zhao D, Yuan K, Zhou G, Wang Y, Xiao Y, Wang C, Xu J, Yang W. 2015. Two new dimeric naphthoquinones with neuraminidase inhibitory activity from Lithospermum erythrorhizon. Nat Prod Res. 29(10):908–913.

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