Biologically Active Metabolites from the Marine Sediment-Derived Fungus Aspergillus flocculosus

被引:20
作者
Yurchenko, Anton N. [1 ]
Phan Thi Hoai Trinh [2 ]
Girich , Elena V. [1 ]
Smetanina, Olga F. [1 ]
Rasin, Anton B. [1 ]
Popov, Roman S. [1 ]
Dyshlovoy, Sergey A. [1 ,3 ,4 ,5 ]
von Amsberg, Gunhild [4 ,5 ]
Menchinskaya, Ekaterina S. [1 ]
Tran Thi Thanh Van [2 ]
Afiyatullov, Shamil Sh. [1 ]
机构
[1] Russian Acad Sci, Far Eastern Branch, GB Elyakov Pacific Inst Bioorgan Chem, Prospect 100 Letiya Vladivostoka,159, Vladivostok 690022, Russia
[2] Vietnam Acad Sci & Technol, Nhatrang Inst Technol Res & Applicat, Dept Marine Biotechnol, Nha Trang 650000, Vietnam
[3] Far Eastern Fed Univ, Sch Nat Sci, Sukhanova St 8, Vladivostok 690000, Russia
[4] Univ Med Ctr Hamburg Eppendorf, Lab Expt Oncol, Dept Oncol Hematol & Bone Marrow Transplantat, Sect Pneumol,Hubertus Wald Tumorzentrum, D-20246 Hamburg, Germany
[5] Univ Hosp Hamburg Eppendorf, Martini Klin, Prostate Canc Ctr, D-20246 Hamburg, Germany
基金
俄罗斯科学基金会;
关键词
marine-derived fungi; secondary metabolites; polyketides; drimanes; meroterpenoids; cytotoxicity; NITROBENZOYL SESQUITERPENOIDS; POLYKETIDES; DERIVATIVES; RESISTANCE;
D O I
10.3390/md17100579
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Four new compounds were isolated from the Vietnamese marine sediment-derived fungus Aspergillus flocculosus, one aspyrone-related polyketide aspilactonol G (2), one meroterpenoid 12-epi-aspertetranone D (4), two drimane derivatives (7,9), together with five known metabolites (1,3,5,6,8,10). The structures of compounds 1-10 were established by NMR and MS techniques. The absolute stereoconfigurations of compounds 1 and 2 were determined by a modified Mosher's method. The absolute configurations of compounds 4 and 7 were established by a combination of analysis of ROESY data and coupling constants as well as biogenetic considerations. Compounds 7 and 8 exhibited cytotoxic activity toward human prostate cancer 22Rv1, human breast cancer MCF-7, and murine neuroblastoma Neuro-2a cells.
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页数:12
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