Cantello B C, Cawthorne M A, Cottam G P, Duff P T, Haigh D, Hindley R M, Lister C A, Smith S A, Thurlby P L
SmithKline Beecham Pharmaceuticals, Epsom, Surrey, United Kingdom.
J Med Chem. 1994 Nov 11;37(23):3977-85. doi: 10.1021/jm00049a017.
A series of [(ureidoethoxy)benzyl]-2,4-thiazolidinediones and [[(heterocyclylamino)alkoxy]-benzyl]-2,4-thiazolidinediones was synthesized from the corresponding aldehydes. Compounds from the urea series, exemplified by 16, showed antihyperglycemic potency comparable with known agents of the type such as pioglitazone and troglitazone (CS-045). The benzoxazole 49, a cyclic analogue of 16, was a very potent enhancer of insulin sensitivity, and by modification of the aromatic heterocycle, an aminopyridine, 37, was identified as a lead compound from SAR studies. Evaluation of antihyperglycemic activity together with effects on blood hemoglobin content, to determine the therapeutic index, was performed in 8-day repeat administration studies in genetically obese C57 Bl/6 ob/ob mice. From these studies, BRL 49653 (37) has been selected, on the basis of antihyperglycemic potency combined with enhanced selectivity against reductions in blood hemoglobin content, for further evaluation.
一系列[(脲基乙氧基)苄基]-2,4-噻唑烷二酮和[[(杂环氨基)烷氧基]苄基]-2,4-噻唑烷二酮由相应的醛合成。以16为例的脲系列化合物显示出与吡格列酮和曲格列酮(CS-045)等已知类型药物相当的抗高血糖效力。苯并恶唑49是16的环状类似物,是一种非常有效的胰岛素敏感性增强剂,通过对芳香杂环进行修饰,从构效关系研究中确定氨基吡啶37为先导化合物。在遗传性肥胖的C57 Bl/6 ob/ob小鼠中进行了为期8天的重复给药研究,评估抗高血糖活性以及对血液血红蛋白含量的影响,以确定治疗指数。基于抗高血糖效力以及对血液血红蛋白含量降低的增强选择性,从这些研究中选择了BRL 49653(37)进行进一步评估。