氮唑类化合物作为Notum羧酸酯酶抑制剂的QSAR对接

Amuthalakshmi Sivaperuman, Ramalakshmi Natarajan, Manimegalai P, A. Subramani, Puratchikody Ayarivan
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引用次数: 0

摘要

羧酸酯酶Notum是Wnt信号的负调控因子。Notum羧酸酯酶是一种羧酸酯水解酶,通过去棕榈酰化反应作为Wnt蛋白的负反馈调节器。了解Wnt的调控途径是非常重要的,因为反过来,Wnt信号的错误调控是癌症和其他退行性疾病的一个信号。Wnt抑制在结直肠癌的控制中具有重要意义。在本研究中,我们使用多元回归分析对一系列报道的具有羧酸酯酶Notum抑制活性的化合物进行了QSAR分析。从文献报道中提取了83个具有羧基Notum抑制值的吡咯衍生物化合物数据集。本研究采用多元线性回归分析,并对模型进行验证。在整个数据集中选择了相关系数(R2)和解释方差(解释方差)最高的多元线性回归(MLR)模型,其中留一(Q2 LOO)和留多(Q2 LMO)预测。所建立的模型进行了内部和外部验证。通过绘制威廉姆斯图来检验预测模型的可靠性。对接方法采用Autodock 4对设计的化合物进行对接,研究配体与受体之间的相互作用。最佳模型的r2值为0.7413,Q2LOO =0.6379, Q2LMO =0.6368。根据生成的QSAR方程设计了新的苯基吡咯烷化合物。利用QSAR方程预测了羧酯酶Notum的抑制活性。使用Autodock对设计的化合物进行羧酸酯酶Notum酯酶对接研究。结果表明,所设计的化合物具有抑制Notum羧化酶的作用。因此,该研究导致了一种新的羧酸酯酶Notum先导化合物的开发。
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QSAR Docking on Azoles as inhibitors of Notum carboxylesterase
Carboxylesterase Notum is a negative regulator of Wnt signaling. Notum carboxylesterase is a carboxylic ester hydrolase enzyme that functions as a negative feedback regulator of Wnt proteins by depalmitoylation reaction. It is of great importance to understand the pathway of Wnt regulation because, conversely, misregulation of Wnt signaling is a telltale sign of cancer and other degenerative diseases. The Wnt inhibition is important in the control of colorectal cancer. In the present study, we carried out a QSAR analysis of a series of reported compounds with carboxylesterase Notum inhibitory activity using multiple regression analysis. A series of 83 compound datasets of pyrrole derivatives with carboxy Notum inhibitory values were taken from the reported literature. The study was performed by conducting multiple linear regression analysis followed by validation of the model. The multiple linear regression (MLR) models with the highest coefficients of correlation (R2) and explained variance in leave-one-out (Q2 LOO) prediction and leave-many-out (Q2 LMO) were selected for the whole dataset. The developed models were subjected to internal and external validation. The reliability of the predicted model was checked by plotting the Williams plot. The docking methodology was performed using Autodock 4 for the designed compounds to study the interaction between the ligand and the receptor. The best model generated exhibited an r2 value of 0.7413, Q2LOO =0.6379, Q2LMO =0.6368. Novel compounds of phenyl pyrrolidine were designed based on generated QSAR equations. The carboxylesterase Notum inhibitory activity was predicted using the QSAR equations. The docking studies were carried out for designed compounds using Autodock against Carboxylesterase Notum esterase. From the results, the designed compounds were found to inhibit Notum Carboxylase. Thus, the study led to the development of a novel lead compound for Carboxylesterase Notum.
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来源期刊
Current Chemical Biology
Current Chemical Biology Medicine-Biochemistry (medical)
CiteScore
1.40
自引率
0.00%
发文量
16
期刊介绍: Current Chemical Biology aims to publish full-length and mini reviews on exciting new developments at the chemistry-biology interface, covering topics relating to Chemical Synthesis, Science at Chemistry-Biology Interface and Chemical Mechanisms of Biological Systems. Current Chemical Biology covers the following areas: Chemical Synthesis (Syntheses of biologically important macromolecules including proteins, polypeptides, oligonucleotides, oligosaccharides etc.; Asymmetric synthesis; Combinatorial synthesis; Diversity-oriented synthesis; Template-directed synthesis; Biomimetic synthesis; Solid phase biomolecular synthesis; Synthesis of small biomolecules: amino acids, peptides, lipids, carbohydrates and nucleosides; and Natural product synthesis).
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