首页> 外文期刊>Bulletin of the Korean Chemical Society >2-Substitiuted Thio-and Amino-5,8-dimethoxy-1,4-naphthoquinones as a Novel Class of Acyl-CoA: Cholestrol Acyltransferase Inhibitors
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2-Substitiuted Thio-and Amino-5,8-dimethoxy-1,4-naphthoquinones as a Novel Class of Acyl-CoA: Cholestrol Acyltransferase Inhibitors

机译:2-取代的硫代和氨基-5,8-二甲氧基-1,4-萘醌作为一类新的酰基辅酶A:胆固醇的酰基转移酶抑制剂

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摘要

A series of 2-alkyl or 2-arylthio-5,8-dimethoxy-1,4-naphthoquinones (2-Thio-DMNQ, 5a-s) and 2-alkylamino-5,8-dimethoxy-1,4-naphthoquinones (2-Amino-DMNQ, 6a-k) was synthesized and evaluated for their ACAT inhibitory activities. Among them, the 2-dodecylthio-DMNQ 51 and 2-isobutylamidoundodecylthio-DMNQ 5r showed the most potent ACAT inhibitory activities with IC50 value of 22.8 and 24.4 μM, respectively. In a structure-activity relationship study, 2-thio-DMNQs with side chains of carbon number 11-15 exhibited significant ACAT inhibitory activities.
机译:一系列2-烷基或2-芳硫基-5,8-二甲氧基-1,4-萘醌(2-Thio-DMNQ,5a-s)和2-烷基氨基-5,8-二甲氧基-1,4-萘醌(合成2-氨基-DMNQ,6a-k)并评估其ACAT抑制活性。其中,2-十二烷基硫基-DMNQ 51和2-异丁基酰胺基十二烷基硫基-DMNQ 5r表现出最强的ACAT抑制活性,IC50值分别为22.8和24.4μM。在结构活性关系研究中,碳数为11-15的侧链的2-thio-DMNQs表现出显着的ACAT抑制活性。

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