Wydysh Edward A, Medghalchi Susan M, Vadlamudi Aravinda, Townsend Craig A
Department of Chemistry, The Johns Hopkins University, Remsen Hall, 3400 North Charles Street, Baltimore, Maryland 21218, USA.
J Med Chem. 2009 May 28;52(10):3317-27. doi: 10.1021/jm900251a.
The incidence of obesity and other diseases associated with an increased triacylglycerol mass is growing rapidly, particularly in the United States. Glycerol 3-phosphate acyltransferase (GPAT) catalyzes the rate-limiting step of glycerolipid biosynthesis, the acylation of glycerol 3-phosphate with saturated long-chain acyl-CoAs. In an effort to produce small molecule inhibitors of this enzyme, a series of benzoic and phosphonic acids was designed and synthesized. In vitro testing of this series has led to the identification of several compounds, in particular 2-(nonylsulfonamido)benzoic acid (15g), possessing moderate GPAT inhibitory activity in an intact mitochondrial assay.
肥胖症以及与三酰甘油质量增加相关的其他疾病的发病率正在迅速上升,尤其是在美国。甘油3-磷酸酰基转移酶(GPAT)催化甘油脂质生物合成的限速步骤,即将甘油3-磷酸与饱和长链酰基辅酶A进行酰化反应。为了制备该酶的小分子抑制剂,设计并合成了一系列苯甲酸和膦酸。对该系列化合物进行的体外测试已鉴定出几种化合物,特别是2-(壬基磺酰胺基)苯甲酸(15g),在完整线粒体测定中具有中等的GPAT抑制活性。