NEUROFARBA Dept., Sezione di Scienze Farmaceutiche, University of Florence , Sesto Fiorentino (Florence) , Italy.
Expert Opin Ther Pat. 2019 Oct;29(10):817-827. doi: 10.1080/13543776.2019.1670812. Epub 2019 Oct 1.
: Glaucoma is a group of progressive optic neuropathies in which elevated intraocular pressure (IOP) as a consequence of an increased aqueous humor (AH) outflow resistance, is the main and only clinically modifiable risk factor for its development and progression. Relaxing Trabecular meshwork (TM) tissue, Rho-Kinase (ROCK) inhibitors directly decrease resistance in the conventional AH outflow, thus resulting in a significant IOP-lowering effect. : The progress made in the field of ROCK inhibitors for glaucoma treatment will be discussed, referring to the recent patent literature published mainly in the last 3 years. Development and last studies conducted on the recently approved ripasudil and netarsudil will be described, along with newly reported combinations with other antiglaucoma agents. New molecular entities as ROCK inhibitors will be reported as well as new biological approaches to affect the Rho/ROCK pathway. : With three drugs currently available on the market belonging to this class, ROCK inhibitors have been definitely validated as therapeutic agents for glaucoma treatment. The literature of the last 3 years confirmed the success of the soft-drug and bis-functional approaches in the design of ROCK inhibitors. However, few completely new molecular scaffolds have been reported.
青光眼是一组进行性视神经病变,其中眼内压(IOP)升高是由于房水(AH)流出阻力增加所致,是其发展和进展的主要且唯一可临床改变的危险因素。松弛小梁网(TM)组织,Rho-激酶(ROCK)抑制剂直接降低传统 AH 流出的阻力,从而导致显著的眼压降低作用。本文将主要讨论最近 3 年来发表的专利文献中关于 ROCK 抑制剂在青光眼治疗方面的进展。将描述最近批准的 ripasudil 和 netarsudil 以及与其他抗青光眼药物联合使用的最新研究进展,以及新报道的组合。将报告新的 ROCK 抑制剂作为新的分子实体以及影响 Rho/ROCK 途径的新的生物学方法。目前市场上有三种属于这一类的药物,ROCK 抑制剂已被确认为治疗青光眼的有效药物。过去 3 年的文献证实了软药物和双功能方法在 ROCK 抑制剂设计中的成功。然而,报道的全新分子支架很少。