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PDE4 抑制剂临床试验概述:2010 年至 2022 年初。

An Overview of PDE4 Inhibitors in Clinical Trials: 2010 to Early 2022.

机构信息

NEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Via Ugo Schiff 6, 50019 Sesto Fiorentino, Italy.

Department of Drug and Health Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.

出版信息

Molecules. 2022 Aug 4;27(15):4964. doi: 10.3390/molecules27154964.

Abstract

Since the early 1980s, phosphodiesterase 4 (PDE4) has been an attractive target for the treatment of inflammation-based diseases. Several scientific advancements, by both academia and pharmaceutical companies, have enabled the identification of many synthetic ligands for this target, along with the acquisition of precise information on biological requirements and linked therapeutic opportunities. The transition from pre-clinical to clinical phase was not easy for the majority of these compounds, mainly due to their significant side effects, and it took almost thirty years for a PDE4 inhibitor to become a drug i.e., Roflumilast, used in the clinics for the treatment of chronic obstructive pulmonary disease. Since then, three additional compounds have reached the market a few years later: Crisaborole for atopic dermatitis, Apremilast for psoriatic arthritis and Ibudilast for Krabbe disease. The aim of this review is to provide an overview of the compounds that have reached clinical trials in the last ten years, with a focus on those most recently developed for respiratory, skin and neurological disorders.

摘要

自 20 世纪 80 年代初以来,磷酸二酯酶 4(PDE4)一直是治疗炎症相关疾病的有吸引力的靶标。学术界和制药公司的多项科学进展,使人们能够识别出许多针对该靶标的合成配体,并获得有关生物需求和相关治疗机会的精确信息。对于这些化合物中的大多数来说,从临床前阶段到临床阶段的过渡并不容易,主要是由于它们的副作用显著,几乎花了三十年的时间才使一种 PDE4 抑制剂成为药物,即罗氟司特,用于治疗慢性阻塞性肺病。此后,又有三种化合物在几年后上市:他克莫司用于治疗特应性皮炎,阿普司特用于治疗银屑病关节炎,伊布地尔用于治疗克拉伯病。本文综述的目的是概述过去十年中进入临床试验的化合物,重点介绍最近开发用于治疗呼吸、皮肤和神经疾病的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39a6/9370432/896e7cf3c1ef/molecules-27-04964-g001.jpg

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