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PDE4 抑制剂:通过多种结构类别对命中化合物进行剖析。

PDE4 Inhibitors: Profiling Hits through the Multitude of Structural Classes.

机构信息

Institute of Pharmaceutical Science, King's College London, Stamford Street, London SE1 9NH, UK.

School of Health, Sport and Bioscience, University of East London, London E15 4LZ, UK.

出版信息

Int J Mol Sci. 2023 Jul 15;24(14):11518. doi: 10.3390/ijms241411518.

Abstract

Cyclic nucleotide phosphodiesterases 4 (PDE4) are a family of enzymes which specifically promote the hydrolysis and degradation of cAMP. The inhibition of PDE4 enzymes has been widely investigated as a possible alternative strategy for the treatment of a variety of respiratory diseases, including chronic obstructive pulmonary disease and asthma, as well as psoriasis and other autoimmune disorders. In this context, the identification of new molecules as PDE4 inhibitors continues to be an active field of investigation within drug discovery. This review summarizes the medicinal chemistry journey in the design and development of effective PDE4 inhibitors, analyzed through chemical classes and taking into consideration structural aspects and binding properties, as well as inhibitory efficacy, PDE4 selectivity and the potential as therapeutic agents.

摘要

环核苷酸磷酸二酯酶 4(PDE4)是一类酶,可特异性促进 cAMP 的水解和降解。抑制 PDE4 酶已被广泛研究作为治疗多种呼吸系统疾病的一种可能的替代策略,包括慢性阻塞性肺疾病和哮喘,以及银屑病和其他自身免疫性疾病。在这种情况下,作为 PDE4 抑制剂的新分子的鉴定在药物发现中仍然是一个活跃的研究领域。本综述总结了在设计和开发有效 PDE4 抑制剂方面的药物化学历程,通过化学类别进行分析,并考虑了结构方面和结合特性以及抑制效力、PDE4 选择性和作为治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cd5/10380597/e8711c8f75c9/ijms-24-11518-g001.jpg

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