Department of Physical Chemistry, University of Valencia, Av. Vicente Estelles s/n, 46100 Burjassot (Valencia), Spain.
Instituto de Tecnología Química (UPV-CSIC) Universidad Politécnica de Valencia Av. Naranjos s/n, 46022 Valencia, Spain.
J Chem Inf Model. 2021 Jun 28;61(6):3091-3108. doi: 10.1021/acs.jcim.0c01468. Epub 2021 May 17.
Janus kinases (JAKs) are a family of proinflammatory enzymes able to mediate the immune responses and the inflammatory cascade by modulating multiple cytokine expressions as well as various growth factors. In the present study, the inhibition of the JAK-signal transducer and activator of transcription (STAT) signaling pathway is explored as a potential strategy for treating autoimmune and inflammatory disorders. A computationally driven approach aimed at identifying novel JAK inhibitors based on molecular topology, docking, and molecular dynamics simulations was carried out. For the best candidates selected, the inhibitory activity against JAK2 was evaluated . Two hit compounds with a novel chemical scaffold, (IC = 0.81 μM) and (IC = 0.64 μM), showed promising results when compared with the reference drug Tofacitinib (IC = 0.031 μM).
Janus 激酶(JAKs)是一组促炎酶,能够通过调节多种细胞因子的表达以及各种生长因子来介导免疫反应和炎症级联反应。在本研究中,抑制 JAK-信号转导子和转录激活子(STAT)信号通路被探索作为治疗自身免疫和炎症性疾病的一种潜在策略。进行了一种基于分子拓扑、对接和分子动力学模拟的计算驱动方法,旨在鉴定新型 JAK 抑制剂。对所选最佳候选物进行了针对 JAK2 的抑制活性评估。两种具有新型化学结构骨架的命中化合物(IC = 0.81 μM)和(IC = 0.64 μM)与参考药物托法替尼(IC = 0.031 μM)相比,显示出有希望的结果。