| Literature DB >> 30078607 |
Patima Phainuphong1, Vatcharin Rukachaisirikul2, Saowanit Saithong1, Souwalak Phongpaichit3, Jariya Sakayaroj4, Chutima Srimaroeng5, Atcharaporn Ontawong6, Acharaporn Duangjai7, Paradorn Muangnil8, Chatchai Muanprasat8.
Abstract
One new pyrrolidine derivative, asperidine A (1), and two new piperidine derivatives, asperidines B (2) and C (3), were isolated from the soil-derived fungus Aspergillus sclerotiorum PSU-RSPG178 together with two known alkaloids. Compound 3 possessed an unprecedented 7-oxa-1-azabicyclo[3.2.1]octane skeleton with four chiral centers. Their structures were determined by spectroscopic evidence. The absolute configurations of compounds 2 and 3 were established using Mosher's method and further confirmed for compound 3 by X-ray crystallographic data. Compound 2 dose-dependently inhibited the CFTR-mediated chloride secretion in T84 cells with an IC50 value of 0.96 μM whereas 3 displayed the same activity with the IC50 value of 58.62 μM. Compounds 2 and 3 also significantly reduced intracellular ROS under both normal and H2O2-treated conditions compared with their respective controls in a dose-dependent manner without cytotoxic effect on Caco-2 cells. In addition, compound 3 was inactive against noncancerous Vero cells whereas compound 2 was considered to be inactive with the IC50 value of >10 μM.Entities:
Keywords: Antioxidant; Aspergillus sclerotiorum; CFTR inhibitor; Cytotoxicity; Piperidine derivative; Pyrrolidine derivative
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Year: 2018 PMID: 30078607 DOI: 10.1016/j.bmc.2018.07.036
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641