Journal
FITOTERAPIA
Volume 82, Issue 5, Pages 777-781Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.fitote.2011.04.002
Keywords
Fusarium oxysporum; Oxysporidinone analogues; Cytotoxicity; Antibacterial
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Funding
- National Key Basic Research Project of China [2009CB522300]
- MOST [2007DFB31620]
- Chinese Academy Science [KSCX2-YW-G-074-04]
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A new oxysporidinone analogue (1) and a new 3-hydroxyl-2-piperidinone derivative (2), along with the known compounds (-)-4,6'-anhydrooxysporidinone (3), (+)-fusarinolic acid (4), gibepyrone D (5), beauvercin (6),cerevisterol (7). fusaruside (8), and (25,2'R,3R,3'E,4E,8E)-1-O-D-glucopyranosyl-2-N-(2'-hydroxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8-sphingadienine (9) were isolated from Fusarium oxysporum. Compounds 1-9 were evaluated for cytotoxicity using the MTT method against cancer cell lines, PC-3, PANC-1, and A549. Beauvericin showed cytotoxicity against PC-3, PANC-1, and A549 with IC(50) value of 49.5 +/- 3.8, 47.2 +/- 2.9, and 10.4 +/- 1.6 mu M, respectively. Beauvericin also exhibited anti-bacterial activity towards methicillin-resistant Staphylococcus aureus (MIC = 3.125 mu g/mL) and Bacillus subtilis (MIC = 3.125 mu g/mL). (C) 2011 Elsevier B.V. All rights reserved.
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