Tonghan ZhuZhenyu LuJie FanLiping WangGuoliang ZhuYi WangXia LiKui HongPawinee PiyachaturawatArthit ChairoungduaWeiming ZhuShandong University, WeihaiWuhan UniversityOcean University of ChinaChinese Academy of SciencesMahidol University2019-08-232019-08-232018-01-26Journal of Natural Products. Vol.81, No.1 (2018), 2-915206025016338642-s2.0-85041213491https://repository.li.mahidol.ac.th/handle/20.500.14594/45264© 2017 The American Chemical Society and American Society of Pharmacognosy. Seven new ophiobolins (1-5, 12, and 14) along with the 11 known analogues (6-11, 13, 15-18) were isolated from the ethyl acetate extracts of the liquid and solid cultures of the mangrove fungus Aspergillus ustus 094102. The structures including the absolute configurations of the seven new compounds were elucidated by spectroscopic analysis, chemical methods, and quantum ECD calculations. Compounds 4-8 and 11-15 showed cytotoxicities against the G3K, MCF-7, MD-MBA-231, MCF/Adr, A549, and HL-60 human cancer cell lines with the IC 50 values ranging from 0.6 to 9.5 μM.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemistryMedicinePharmacology, Toxicology and PharmaceuticsOphiobolins from the Mangrove Fungus Aspergillus ustusArticleSCOPUS10.1021/acs.jnatprod.7b00335