应用模拟退火-支持向量机预测PTP1B抑制剂抗糖尿病作用的QSAR模型

Hanif Fadhlurrahman, Azka Khoirunnisa, I. Kurniawan
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摘要

糖尿病是一种以血糖升高为特征的疾病。这种疾病可以处理长期损害,如各种器官功能障碍和衰竭。在印度尼西亚,糖尿病是导致死亡的主要原因之一,有1 000多万人患有糖尿病。到目前为止,还没有药物可以治愈糖尿病。到目前为止,糖尿病患者必须为自己的日常生活负责。要找到治疗糖尿病的方法,需要进行药物研发。蛋白酪氨酸磷酸酶1B (PTP1B)是一种有前景的抗糖尿病靶点抑制剂。药物发现需要花费大量的时间和精力,因此,可以使用定量构效关系(QSAR)等计算机方法来加速这一过程。我们的目标是利用模拟退火(SA)-支持向量机(SVM)方法建立PTP1B抑制剂抗糖尿病的QSAR模型。通过从每个化合物中选择smile从ChEMBL数据库中检索数据。通过使用PaDEL计算smile,我们得到每个化合物的1443个描述符,通过使用SA,我们减少了描述符的数量。最佳结果表明,SA从1443个描述符中选择了600个描述符。SVM上的RBF核的准确率为94.508%,F1分数为95.048%,AUC为0.943,具有最佳值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
QSAR Model for Prediction PTP1B Inhibitor as Anti-diabetes Mellitus using Simulated Annealing-Support Vector Machine
Diabetes mellitus or diabetes is a kind of disease characterized by a raised in blood sugar. This disease can deal with long-term damage, such as dysfunction and failure of various organs. In Indonesia, diabetes is one of the major causes of death, with more than 10 million people living with diabetes. To date, no drug can cure diabetes. So far, people with diabetes must take responsibility for their daily routine. Drug discovery is needed to find the cure for diabetes. protein tyrosine phosphatase 1B (PTP1B) is one inhibitor that proved as a promising target for anti-diabetes Mellitus. Drug discovery takes a lot of time and effort, and thus, in silico methods, such as quantitative structure-activity relationship (QSAR), can be used to accelerate this process. We aim to build a QSAR model of PTP1B inhibitor as anti-diabetes Mellitus using the simulated annealing (SA)-Support Vector Machine (SVM) method. The data were retrieved from the ChEMBL database by selecting the SMILES from each compound. By calculating the SMILES using PaDEL, we got 1443 descriptors for each compound, and by using SA, we decreased the number of descriptors. The best result shows that SA selected 600 descriptors out of 1443 descriptors for each compound. The RBF kernel on SVM has the best value with accuracy, F1 score, and AUC of 94.508%, 95.048%, and 0.943, respectively.
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