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从黄槐中提取的生物活性化合物有望成为治疗类风湿性关节炎的 Janus 激酶(JAKs)抑制剂

Bioactive Compounds from Nyctanthes arbor tristis Linn as Potential Inhibitors of Janus Kinases (JAKs) Involved in Rheumatoid Arthritis.

机构信息

School of Life Sciences, B.S. Abdur Rahman Crescent Institute of Science and Technology, Chennai, 600048, Tamil Nadu, India.

出版信息

Appl Biochem Biotechnol. 2023 Jan;195(1):314-330. doi: 10.1007/s12010-022-04121-1. Epub 2022 Sep 9.

Abstract

Nyctanthes arbor tristis L (NAT) is one of the herbal plants whose parts are commonly used to treat diverse ailment including RA. Although the etiology of the autoimmune disorder RA is still unclear, actions of cytokines have been greatly associated with the mechanism of RA. Despite the huge development of drugs to combat this disorder, the search for alternative medicine is increasing due to the adverse effects of these synthetic drugs. Here, the ability of 30 selected bioactive compounds from the parts of NAT to bind effectively to target proteins of the Janus kinases as a potent inhibitor was predicted in an in silico manner through molecular docking procedure using Autodock 4.2.6 and their interactions visualized using Discovery Studio, followed by evaluating the physiochemical and ADMET properties of compounds of the lowest binding energy comparable to the reference drug baricitinib. Comparing the predicted target information with the standard drug baricitinib, 7 bioactive compounds may be potential lead drug for the treatment of RA owing to their lowest binding energy ranging from - 7.0 kcal/mol to - 10.49 kcal/mol and their pharmacokinetics properties. This can be used for further in vivo and in vitro studies to establish their potency as JAKs inhibitors to treat RA.

摘要

黄花夹竹桃(NAT)是一种草药植物,其部分常用于治疗多种疾病,包括类风湿关节炎。尽管自身免疫性疾病类风湿关节炎的病因尚不清楚,但细胞因子的作用与类风湿关节炎的发病机制密切相关。尽管有大量的药物用于对抗这种疾病,但由于这些合成药物的不良反应,对替代药物的研究也在不断增加。在这里,通过分子对接程序,使用 Autodock 4.2.6 从 NAT 的部分中预测了 30 种具有生物活性的化合物有效地与 Janus 激酶的靶蛋白结合的能力,作为一种有效的抑制剂,并使用 Discovery Studio 可视化它们的相互作用,然后评估与参考药物巴瑞替尼相比具有最低结合能的化合物的物理化学和 ADMET 性质。将预测的靶标信息与标准药物巴瑞替尼进行比较,有 7 种生物活性化合物可能是治疗类风湿关节炎的潜在先导药物,因为它们的最低结合能范围为-7.0 kcal/mol 至-10.49 kcal/mol,且具有良好的药代动力学性质。这可以用于进一步的体内和体外研究,以确定它们作为 JAK 抑制剂治疗类风湿关节炎的效力。

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