Augustyns K, Van der Veken P, Senten K, Haemers A
Department of Medicinal Chemistry, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.
Curr Med Chem. 2005;12(8):971-98. doi: 10.2174/0929867053507298.
In this review the structural and functional aspects of dipeptidyl peptidase IV (DPP IV) will be described, and the therapeutic potential of DPP IV inhibitors will be highlighted. DPP IV will be situated in clan SC, a group of serine proteases that contains several proline specific peptidases. Structural aspects of DPP IV and its interaction with different types of inhibitors are recently revealed by the publication of several crystal structures. Especially the design and development of new DPP IV inhibitors based on the three-dimensional structure, substrate specificity and catalytic mechanism will be discussed. In the last years there was an important development of new pyrrolidine-2-nitriles with very promising therapeutic properties for the treatment of type 2 diabetes. The role of DPP IV in peptide metabolism of members of the PACAP/glucagon peptide family, neuropeptides and chemokines has been thoroughly investigated during recent years. This is directly related to the promising therapeutic potential of DPP IV inhibitors in the treatment of type 2 diabetes and in the treatment of immunological disorders. Several inhibitors are currently under investigation in clinical trials for the treatment of type 2 diabetes and represent a new class of drugs for the treatment of this disease.
在本综述中,将描述二肽基肽酶IV(DPP IV)的结构和功能方面,并强调DPP IV抑制剂的治疗潜力。DPP IV属于SC家族,这是一组丝氨酸蛋白酶,其中包含几种脯氨酸特异性肽酶。最近,通过几个晶体结构的发表揭示了DPP IV的结构方面及其与不同类型抑制剂的相互作用。尤其将讨论基于三维结构、底物特异性和催化机制的新型DPP IV抑制剂的设计与开发。在过去几年中,新型吡咯烷-2-腈有了重要进展,其在治疗2型糖尿病方面具有非常有前景的治疗特性。近年来,已对DPP IV在垂体腺苷酸环化酶激活肽/胰高血糖素肽家族成员、神经肽和趋化因子的肽代谢中的作用进行了深入研究。这与DPP IV抑制剂在治疗2型糖尿病和免疫紊乱方面有前景的治疗潜力直接相关。目前有几种抑制剂正在进行治疗2型糖尿病的临床试验研究,它们代表了治疗该疾病的一类新型药物。