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Identification and Validation of a Selective Small Molecule Inhibitor Targeting the Diacylglycerol Acyltransferase 2 Activity

Authors
Kim, Mun OckLee, Su UiLee, Hyun-JunChoi, KwangmanKim, HyeongkiLee, SangkuOh, Soo JinKim, SunhongKang, Jong SoonLee, Hyun SunKwak, Young-ShinCho, Sungchan
Issue Date
Jul-2013
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
metabolic disease; triacylglycerol; diacylglycerol acyltransferase 2; small molecule inhibitor; isatin
Citation
BIOLOGICAL & PHARMACEUTICAL BULLETIN, v.36, no.7, pp.1167 - 1173
Indexed
SCIE
SCOPUS
Journal Title
BIOLOGICAL & PHARMACEUTICAL BULLETIN
Volume
36
Number
7
Start Page
1167
End Page
1173
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/102758
DOI
10.1248/bpb.b13-00152
ISSN
0918-6158
Abstract
Diacylglycerol acyltransferase 2 (DGAT2) is one of two distinct DGAT enzymes that catalyze the last step in triacylglycerol (TG) synthesis. Findings from previous studies suggest that inhibition of DGAT2 is a promising strategy for the treatment of hepatic steatosis and insulin resistance. Here, we identified compound 122 as a potent and selective inhibitor of human DGAT2, which appeared to act competitively against oleoyl-CoA in vitro. The selective inhibition of DGAT2 was also confirmed by the reductions in enzymatic activity and de novo TG synthesis in DGAT2-overexpressing HEK293 cells and hepatic cells HepG2. Compound 122, as a newly identified inhibitor of DGAT2, will be useful for the research on DGAT2-related lipid metabolism as well as the development of therapeutic drug for several metabolic diseases.
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