| Literature DB >> 27228159 |
Patima Phainuphong, Vatcharin Rukachaisirikul, Saowanit Saithong, Souwalak Phongpaichit, Kawitsara Bowornwiriyapan, Chatchai Muanprasat1, Chutima Srimaroeng2, Acharaporn Duangjai3, Jariya Sakayaroj4.
Abstract
Three new lovastatin analogues (1, 4, and 5) together with four known lovastatin derivatives, namely, lovastatin (2), α,β-dehydrolovastatin (3), α,β-dehydrodihydromonacolin K (6), and α,β-dehydro-4a,5-dihydromonacolin L (7), were isolated from the soil-derived fungus Aspergillus sclerotiorum PSU-RSPG178. Their structures were established using spectroscopic evidence. Compound 5 exhibited the most potent activity against HMG-CoA reductase, with an IC50 value of 387 μM. In addition, the present study indicated the direct interaction of compound 5 with HMG-CoA reductase. Compound 5 was considered to be noncytotoxic against noncancerous Vero cells, with an IC50 value of 40.0 μM, whereas compound 2 displayed much stronger activity, with an IC50 value of 2.2 μM.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27228159 DOI: 10.1021/acs.jnatprod.5b00961
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050