Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58351
Title: Asperidines A–C, pyrrolidine and piperidine derivatives from the soil-derived fungus Aspergillus sclerotiorum PSU-RSPG178
Authors: Patima Phainuphong
Vatcharin Rukachaisirikul
Saowanit Saithong
Souwalak Phongpaichit
Jariya Sakayaroj
Chutima Srimaroeng
Atcharaporn Ontawong
Acharaporn Duangjai
Paradorn Muangnil
Chatchai Muanprasat
Authors: Patima Phainuphong
Vatcharin Rukachaisirikul
Saowanit Saithong
Souwalak Phongpaichit
Jariya Sakayaroj
Chutima Srimaroeng
Atcharaporn Ontawong
Acharaporn Duangjai
Paradorn Muangnil
Chatchai Muanprasat
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Jan-2018
Abstract: © 2018 Elsevier Ltd 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 IC50value of 0.96 μM whereas 3 displayed the same activity with the IC50value 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 IC50value of >10 μM.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85050890135&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/58351
ISSN: 14643391
09680896
Appears in Collections:CMUL: Journal Articles

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