Morrell J A, Orme J, Butlin R J, Roche T E, Mayers R M, Kilgour E
AstraZeneca, Alderley Park, Macclesfield, Cheshire, SK10 4TG, U.K.
Biochem Soc Trans. 2003 Dec;31(Pt 6):1168-70. doi: 10.1042/bst0311168.
The PDH (pyruvate dehydrogenase) multi-enzyme complex catalyses a key regulatory step in oxidative glycolysis. Phosphorylation of the E1 subunit of the complex on serine residues results in the inactivation of enzyme activity. A family of four dedicated PDH kinase isoenzymes exists, each of which displays a distinct tissue-specific expression profile. AZD7545 is one of a series of PDH kinase inhibitors developed for the treatment of type 2 diabetes. The isoenzyme-selectivity profile of AZD7545 and related compounds is described and the consequences for their in vivo mode of action are discussed.
丙酮酸脱氢酶(PDH)多酶复合体催化氧化糖酵解中的一个关键调控步骤。该复合体E1亚基丝氨酸残基的磷酸化会导致酶活性失活。存在一个由四种特异性丙酮酸脱氢酶激酶同工酶组成的家族,每种同工酶都表现出独特的组织特异性表达谱。AZD7545是为治疗2型糖尿病而研发的一系列丙酮酸脱氢酶激酶抑制剂之一。本文描述了AZD7545及相关化合物的同工酶选择性谱,并讨论了其对体内作用模式的影响。