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HDAC6 检测器:用于评估化合物作为潜在组蛋白去乙酰化酶 6 抑制剂的在线应用程序。

HDAC6 detector: online application for evaluating compounds as potential histone deacetylase 6 inhibitors.

作者信息

Tinkov O V, Grigorev V Y, Grigoreva L D, Osipov V N, Kolotaev A V, Khachatryan D S

机构信息

Department of Pharmacology and Pharmaceutical Chemistry, Medical Faculty, Shevchenko Transnistria State University, Tiraspol, Moldova.

Institute of Physiologically Active Compounds, Federal Research Center for Problems of Chemical Physics and Medical Chemistry, Russian Academy of Sciences, Chernogolovka, Russia.

出版信息

SAR QSAR Environ Res. 2023 Jul-Sep;34(8):619-637. doi: 10.1080/1062936X.2023.2244419. Epub 2023 Aug 11.

Abstract

The HDAC6 (histone deacetylase 6) enzyme plays a key role in many biological processes, including cell division, apoptosis, and immune response. To date, HDAC6 inhibitors are being developed as effective drugs for the treatment of various diseases. In this work, adequate QSAR models of HDAC6 inhibitors are proposed. They are integrated into the developed application HDAC6 Detector, which is freely available at https://ovttiras-hdac6-detector-hdac6-detector-app-yzh8y5.streamlit.app/. The web application HDAC6 Detector can be used to perform virtual screening of HDAC6 inhibitors by dividing the compounds into active and inactive ones relative to the reference vorinostat compound (IC = 10.4 nM). The web application implements a structural interpretation of the developed QSAR models. In addition, the application can evaluate the compliance of a compound with Lipinski's rule. The developed models are used for virtual screening of a series of 12 new hydroxamic acids, namely, the derivatives of 3-hydroxyquinazoline-4(3)-ones and 2-aryl-2,3-dihydroquinazoline-4(1)-ones. In vitro evaluation of the inhibitory activity of this series of compounds against HDAC6 allowed us to confirm the results of virtual screening and to select promising compounds V-6 and V-11, the IC of which is 0.99 and 0.81 nM, respectively.

摘要

组蛋白去乙酰化酶6(HDAC6)在许多生物过程中起着关键作用,包括细胞分裂、细胞凋亡和免疫反应。迄今为止,HDAC6抑制剂正被开发为治疗各种疾病的有效药物。在这项工作中,提出了HDAC6抑制剂的适当定量构效关系(QSAR)模型。它们被整合到已开发的应用程序HDAC6 Detector中,该应用程序可在https://ovttiras-hdac6-detector-hdac6-detector-app-yzh8y5.streamlit.app/上免费获取。网络应用程序HDAC6 Detector可用于通过将化合物相对于参考伏立诺他化合物(IC = 10.4 nM)分为活性和非活性化合物来进行HDAC6抑制剂的虚拟筛选。该网络应用程序对所开发的QSAR模型进行结构解释。此外,该应用程序可以评估化合物是否符合Lipinski规则。所开发的模型用于对一系列12种新的异羟肟酸进行虚拟筛选,即3-羟基喹唑啉-4(3)-酮和2-芳基-2,3-二氢喹唑啉-4(1)-酮的衍生物。对该系列化合物对HDAC6的抑制活性进行体外评估,使我们能够确认虚拟筛选的结果,并选择有前景的化合物V-6和V-11,其IC分别为0.99和0.81 nM。

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