A new antimicrobial indoloditerpene from a marine-sourced fungus aspergillus versicolor ZZ761

References

• Chang YW, Yuan CM, Zhang J, Liu S, Cao P, Hua HM, Di YT, Hao XJ. 2016. Speramides A–B, two new prenylated indole alkaloids from the freshwater-derived fungus Aspergillus ochraceus KM007. Tetrahedron Lett. 57(45):4952–4955.
   Web of Science ®Google Scholar
• Chen C, Ye YH, Wang RJ, Zhang YL, Wu C, Debnath CS, Ma ZJ, Wang JD, Wu M. 2018. Streptomyces nigra sp. nov. is a novel actinobacterium isolated from mangrove soil and exerts a potent antitumor activity in vitro. Front Microbiol. 9:1587.
   PubMed Web of Science ®Google Scholar
• Fan YQ, Wang Y, Liu PP, Fu P, Zhu TH, Wang W, Zhu WM. 2013. Indole-diterpenoids with anti-H1N1 activity from the aciduric fungus Penicillium camemberti OUCMDZ-1492. J Nat Prod. 76(7):1328–1336.
   PubMed Web of Science ®Google Scholar
• Gao N, Shang ZC, Yu P, Luo J, Jian KL, Kong LY, Yang MH. 2017. Alkaloids from the endophytic fungus Penicillium brefeldianum and their cytotoxic activities. Chinese Chem Lett. 28(6):1194–1199.
   Web of Science ®Google Scholar
• Harms H, Rempel V, Kehraus S, Kaiser M, Hufendiek P, Müller CE, König GM. 2014. Indoloditerpenes from a marine-​derived fungal strain of Dichotomomyces cejpii with antagonistic activity at GPR18 and cannabinoid receptors. J Nat Prod. 77(3):673–677.
   PubMed Web of Science ®Google Scholar
• Hensens OD, Ondeyka JG, Dombrowski AW, Ostlind DA, Zink DL. 1999. Isolation and structure of nodulisporic acid A1 and A2, novel insecticides from a Nodulisporium sp. Tetrahedron Lett. 40(30):5455–5458.
   Web of Science ®Google Scholar
• Hosoe T, Itabashi T, Kobayashi N, Udagawa SI, Kawai KI. 2006. Three new types of indoloditerpenes, emindole PA-​PC, from Emericella purpurea. Revision of the structure of emindole PA. Chem Pharm Bull. 54(2):185–187.
   PubMed Web of Science ®Google Scholar
• Huang XH, Nishida H, Tomoda H, Tabata N, Shiomi K, Yang DJ, Takayanagi H, Omura S. 1995. Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. II. Structure elucidation of terpendoles A, B, C and D. J Antibiot. 48(1):5–11.
   PubMed Web of Science ®Google Scholar
• Itabashi T, Nozawa K, Nakajima S, Kawai K. 1993. A new azaphilone, falconensin H, from Emericella falconensis. Chem Pharm Bull. 41(11):2040–2041.
   Web of Science ®Google Scholar
• Ji YB, Yin JD, Zheng T, Guan X, Li B, Liu D. 2018. Antibacterial secondary metabolites from the marine-derived fungus Aspergillus violaceus WZXY-m64-17. Chin J Mar Drugs. 37:7–11.
   Google Scholar
• Kato H, Nakahara T, Sugimoto K, Matsuo K, Kagiyama I, Frisvad JC, Sherman DH, Williams RM, Tsukamoto S. 2015. Isolation of notoamide S and enantiomeric 6-epi-stephacidin A from the fungus Aspergillus amoenus: biogenetic implications. Org Lett. 17(3):700–703.
   PubMed Web of Science ®Google Scholar
• Kato H, Yoshida T, Tokue T, Nojiri Y, Hirota H, Ohta T, Williams RM, Tsukamoto S. 2007. Notoamides A–D: prenylated indole alkaloids isolated from a marine-derived fungus, Aspergillus sp. Angew Chem Int Ed. 46(13):2254–2256.
   PubMed Web of Science ®Google Scholar
• Kimura Y, Nishibe M, Nakajima H, Hamasaki T, Shigemitsu N, Sugawara F, Stout TJ, Clardy J. 1992. Emeniveol; A new pollen growth inhibitor from the fungus, Emericella nivea. Tetrahedron Lett. 33(46):6987–6990.
   Web of Science ®Google Scholar
• Kornsakulkarn J, Saepua S, Srichomthong K, Supothina S, Thongpanchang C. 2012. New mycotoxins from the scale insect fungus Aschersonia coffeae Henn. BCC 28712. Tetrahedron. 68(40):8480–8486.
   Web of Science ®Google Scholar
• Kumar S, Stecher G, Tamura K. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Bio Evol. 33(7):1870–1874.
   PubMed Web of Science ®Google Scholar
• Li C, Gloer JB, Wicklow DT. 2003. Thiersindoles A-C: new indole diterpenoids from Penicillium thiersii. J Nat Prod. 66(9):1232–1235.
   PubMed Web of Science ®Google Scholar
• Liu T, Meyer SLF, Chitwood DJ, Chauhan KR, Dong D, Zhang TT, Li J, Liu WC. 2017. New nematotoxic indoloditerpenoid produced by Gymnoascus reessii za-130. J Agric Food Chem. 65(15):3127–3132.
   PubMed Web of Science ®Google Scholar
• Nozawa K, Sekita S, Harada M, Udagawa S, Kawai K. 1989. Studies of fungal products. Part XXVI. Isolation and structures of two new indoloditerpenes related to aflavinine from a microsclerotium-​producing strain of Aspergillus flavus. Chem Pharm Bull. 37(3):626–630.
   Web of Science ®Google Scholar
• Ooike M, Nozawa K, Udagawa SI, Kawai KI. 1997. Structures of a new type of indoloditerpene, petromindole, and a new asterriquinone derivative, PM-​53, from the ascostromata of Petromyces muricatus. Chem Pharm Bull. 45(10):1694–1696.
   Web of Science ®Google Scholar
• Qiao MF, Ji NY, Liu XH, Li K, Zhu QM, Xue QZ. 2010. Indoloditerpenes from an algicolous isolate of Aspergillus oryzae. Biorg Med Chem Lett. 20(19):5677–5680.
   PubMed Web of Science ®Google Scholar
• Steyn PS. 1973. Structure of five dioxopiperazines from Aspergillus ustus. Tetrahedron. 29(1):107–120.
   Web of Science ®Google Scholar
• Tomoda H, Tabata N, Yang DJ, Takayanagi H, Omura S. 1995. Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. III. Production, isolation and structure elucidation of new components. J Antibiot. 48(8):793–804.
   PubMed Web of Science ®Google Scholar
• Tsukamoto S, Kato H, Greshock TJ, Hirota H, Ohta T, Williams RM. 2009. Isolation of Notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp. J Am Chem Soc. 131(11):3834–3835.
   PubMed Web of Science ®Google Scholar
• Tsukamoto S, Kato H, Samizo M, Nojiri Y, Onuki H, Hirota H, Ohta T. 2008. Notoamides F-​K, prenylated indole alkaloids isolated from a marine-​derived Aspergillus sp. J Nat Prod. 71(12):2064–2067.
   PubMed Web of Science ®Google Scholar
• Tsukamoto S, Kawabata T, Kato H, Greshock TJ, Hirota H, Ohta T, Williams RM. 2009. Isolation of antipodal (−)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp. Org Lett. 11(6):1297–1300.
   PubMed Web of Science ®Google Scholar
• Wang KW, Ding P. 2018. New bioactive metabolites from the marine-​derived Fungi Aspergillus. MRMC. 18(13):1072–1094.
   Web of Science ®Google Scholar
• Xin WX, Ye XW, Yu SR, Lian XY, Zhang ZZ. 2012. New capoamycin-type antibiotics and polyene acids from marine Streptomyces fradiae PTZ0025. Mar Drugs. 10(12):2388–2402.
   PubMed Web of Science ®Google Scholar
• Ye XW, Anjum K, Song TF, Wang WW, Yu SR, Huang HC, Lian XY, Zhang ZZ. 2016. A new curvularin glycoside and its cytotoxic and antibacterial analogues from marine actinomycete Pseudonocardia sp. HS7. Nat Prod Res. 30(10):1156–1161.
   PubMed Web of Science ®Google Scholar
• Yoshida O, Tanaka N, Ashida T, Kakudo M, Fukuyama K, Katsube Y. 1979. Structure of demethylsterigmatocystin. Acta Crystallogr B Struct Crystallogr Cryst Chem. B35:1266–1268.
   Google Scholar
• Zhao C, Liu H, Zhu W. 2016. New natural products from the marine-​derived Aspergillus fungi-​A review. Acta Microbiol Sin. 56:331–362.
   PubMedGoogle Scholar
• Zhu F, Lin YC. 2007. Three xanthones from a marine-derived mangrove endophytic fungus. Chem Nat Compd. 43(2):132–135.
   Web of Science ®Google Scholar