Abstract
A novel series of thieno[3,2-d]pyrimidine derivatives were synthesised and their inhibitory effects against diacylglycerol acyltransferase 1 (DGAT-1) were assessed. cis-Isomer 17a showed potent and selective inhibitory activity against DGAT-1 in SF9 cells. In addition, 17a had an acceptable pharmacokinetic profile and accumulated mainly in the small intestine and liver. Oral administration of 17a led to a significant reduction in plasma triacylglycerol level during an oral lipid tolerance test (OLTT) in murine and canine models. Taken together, 17a is a high-quality candidate that deserves further investigation.
Author supplied keywords
Cite
CITATION STYLE
Hong, D. J., Jung, S. H., Kim, J., Jung, D., Ahn, Y. G., Suh, K. H., & Min, K. H. (2020). Synthesis and biological evaluation of novel thienopyrimidine derivatives as diacylglycerol acyltransferase 1 (DGAT-1) inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry, 35(1), 227–234. https://doi.org/10.1080/14756366.2019.1693555
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.