Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591713 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
A new ophiobolin derivative, 3-anhydro-6-hydroxy-ophiobolin A (1), as well as two known ophiobolin derivatives 3-anhydro-ophiobolin A (2) and 3-anhydro-6-epi-ophiobolin A (3) were isolated from the PDB culture of a phytopathogenic fungus Bipolaris oryzae. The structure of 1 was elucidated through 2D NMR and other spectroscopic techniques. Compound 1 exhibited strong antimicrobial activity against Bacille Calmette-Guerin, Bacillus subtilis, Staphylococcus aureus, and methicillin-resistant Staphylococcus aureus with MIC value of 12.5 μg/mL, and potent antiproliferative activity against cell lines HepG2 and K562 with IC50 of 6.49 μM and 4.06 μM, respectively. Further studies on the cytotoxicity of compound 1 against K562 cells demonstrated that it induced apoptosis, observed by flow cytometric method. Preliminary structure-activity relationships of these ophiobolins and the mechanism of apoptosis induced by 1 were analyzed.
Related Topics
Physical Sciences and Engineering
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Authors
Quan-Xin Wang, Jian-Ling Yang, Qiu-Yue Qi, Li Bao, Xiao-Li Yang, Miao-Miao Liu, Pei Huang, Li-Xin Zhang, Ji-Long Chen, Lei Cai, Hong-Wei Liu,