Cioffi Christopher L
a Departments of Basic and Clinical Sciences and Pharmaceutical Sciences , Albany College of Pharmacy and Health Sciences , Albany , NY , USA.
Expert Opin Ther Pat. 2018 Mar;28(3):197-210. doi: 10.1080/13543776.2018.1429408. Epub 2018 Jan 24.
Numerous research groups have developed GlyT-1 inhibitors in the pursuit of providing a novel antipsychotic treatment for schizophrenia. Despite multiple compounds advancing into clinical trials, a GlyT-1 inhibitor has yet to emerge to treat patients. However, the approach remains heavily investigated as it presents potential therapeutic utility for several other CNS and non-CNS-related indications.
This review discusses various GlyT-1 inhibitor chemotypes identified and provides an overview of patent applications filed and published during the period of 2011-2016. The review largely focuses on composition of matter patent applications, although two recently disclosed method of use patents are discussed. Clinical reports are also disseminated.
Mounting clinical failures with schizophrenic patients have blunted enthusiasm for GlyT-1 inhibition as an approach to treat the disease. However, research in the area remains quite active, as therapeutic potential for several additional indications has emerged. There are numerous and diverse GlyT-1 chemotypes now available that exhibit differentiating modes of binding and ligand-target binding kinetics, and this rich diversity of chemical matter may help further elucidate the target's pharmacological role in various indications and lead to the identification of a compound with optimal properties that may someday become a drug.
众多研究团队致力于开发甘氨酸转运体-1(GlyT-1)抑制剂,以期为精神分裂症提供一种新型抗精神病治疗方法。尽管多种化合物已进入临床试验阶段,但尚未有GlyT-1抑制剂用于治疗患者。然而,由于该方法在其他多种中枢神经系统(CNS)及非CNS相关适应症方面具有潜在治疗价值,仍在进行大量研究。
本综述讨论了已鉴定出的多种GlyT-1抑制剂化学类型,并概述了2011年至2016年期间提交和公布的专利申请。本综述主要聚焦于物质组合物专利申请,不过也讨论了两项最近披露的用途专利方法。还传播了临床报告。
在精神分裂症患者中临床失败案例不断增加,这使得人们对GlyT-1抑制作为治疗该疾病方法的热情有所降低。然而,该领域的研究仍相当活跃,因为已发现了其他多种适应症的治疗潜力。目前有众多不同的GlyT-1化学类型,它们表现出不同的结合模式和配体-靶点结合动力学,这种丰富多样的化学物质可能有助于进一步阐明该靶点在各种适应症中的药理作用,并促使鉴定出具有最佳特性的化合物,有望在未来成为药物。