Meroterpenoids from <i>Neosetophoma</i> sp.: A Dioxa[4.3.3]propellane Ring System, Potent Cytotoxicity, and Prolific Expression
Tamam El‐ElimatDepartment of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, JordanHuzefa A. RajaDepartment of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, North Carolina 27402, United StatesSloan AyersDepartment of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, North Carolina 27402, United StatesSteven J. KurinaDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois 60612, United StatesJoanna E. BurdetteDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois 60612, United StatesZachary MattesDepartment of Chemistry, Boston University, Boston, Massachusetts 02215, United StatesRobert C. SabatelleDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, United StatesJeffrey W. BaconDepartment of Chemistry, Boston University, Boston, Massachusetts 02215, United StatesAaron H. ColbyDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, United StatesMark W. GrinstaffDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, United StatesCedric J. PearceMycosynthetix, Inc., Hillsborough, North Carolina 27278, United StatesNicholas H. OberliesDepartment of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, North Carolina 27402, United States
2019en
ABI
Annotatsiya
values while not inducing mitochondrial toxicity at 12.5 μM.
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