QUANTITATIVE STRUCTURE (INHIBITORY) ACTIVITY RELATIONSHIP AND MOLECULAR DOCKING STUDIES OF PHENOLIC ACIDS TO ANGIOTENSIN-CONVERTINGENZYME

GB GONZALES; J VAN CAMP; N AL SHUKOR; D STAUANSSENS; K STRUDS; M ZOTTI; K RAES; G SMAGGHE

首页> 外文期刊>Communications in Agricultural and Applied Biological Sciences >QUANTITATIVE STRUCTURE (INHIBITORY) ACTIVITY RELATIONSHIP AND MOLECULAR DOCKING STUDIES OF PHENOLIC ACIDS TO ANGIOTENSIN-CONVERTINGENZYME

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QUANTITATIVE STRUCTURE (INHIBITORY) ACTIVITY RELATIONSHIP AND MOLECULAR DOCKING STUDIES OF PHENOLIC ACIDS TO ANGIOTENSIN-CONVERTINGENZYME

机译：酚酸与血管紧张素转化酶的定量结构（抑制）活性关系和分子对接研究

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In recent years, considerable research has been done to evaluate the health-promoting activities of plant nutraceuticals. It has been frequently reported that consumption of fruits and vegetables that contain high amounts of phenolic compounds tend toreduce the risks of cardiovascular diseases (Ayaz et al, 2008). Phenolic acids represent a group of secondary plant metabolites that have demonstrated potential for blood pressure-lowering activity both in vitro and in spontaneously hypertensive rats (Alam et al 2013; Al Shukor et al 2013; Geng et al 2010; Thekkumkara et al 2012). These activities have been linked to the inhibition of the angiotensin-converting enzyme (ACE) (Al Shukor et al 2013; Geng et al 2010).

机译：近年来，已经进行了大量的研究来评估植物保健品的健康促进活动。经常有报道说，食用含有大量酚类化合物的水果和蔬菜往往会降低罹患心血管疾病的风险（Ayaz等，2008）。酚酸代表了一组次级植物代谢产物，它们在体外和自发性高血压大鼠中均具有降低血压的潜力（Alam等，2013; Al Shukor等，2013; Geng等，2010; Thekkumkara等，2012）。这些活性与血管紧张素转化酶（ACE）的抑制有关（Al Shukor等，2013; Geng等，2010）。

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《Communications in Agricultural and Applied Biological Sciences》 |2014年第1期|共4页
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GB GONZALES; J VAN CAMP; N AL SHUKOR; D STAUANSSENS; K STRUDS; M ZOTTI; K RAES; G SMAGGHE;
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中图分类农业基础科学;
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1. QUANTITATIVE STRUCTURE (INHIBITORY) ACTIVITY RELATIONSHIP AND MOLECULAR DOCKING STUDIES OF PHENOLIC ACIDS TO ANGIOTENSIN-CONVERTINGENZYME [J] . GB GONZALES, J VAN CAMP, N AL SHUKOR, Communications in Agricultural and Applied Biological Sciences . 2014,第1期

机译：酚酸与血管紧张素转化酶的定量结构（抑制）活性关系和分子对接研究
2. Prediction of anticancer property of bowsellic acid derivatives by quantitative structure activity relationship analysis and molecular docking study [J] . Raghunath Satpathy, R. K. Guru, R. Behera, Journal of Pharmacy and Bioallied Sciences . 2015,第1期

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3. Computational Insights into the Inhibition of Inosine 5′-Monophosphate Dehydrogenase by Mycophenolic Acid Analogs: Three-Dimensional Quantitative Structure–Activity Relationship and Molecular Docking Studies [J] . Na Yang, Jian Wang, Zhi-Wei Wang, Chemical biology and drug design . 2012,第6期

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4. Studies on Quantitative Structure-Activity-Relationship Inhibitory Effects of Benzoic Acid Derivatives on Tyrosinase [C] . Lu Rong, Ma Hai-xia, Liu Wei-ping, 2010 4th International Conference on Bioinformatics and Biomedical Engineering . 2010

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5. Structure-based design of mutant proteins: I. Molecular docking studies of amino acid binding to wild-type aminoacyl-tRNA synthetases. II. Structure-based design of mutant aminoacyl-tRNA synthetases for non-natural amino acid incorporation. [D] . Zhang, Deqiang. 2003

机译：基于结构的突变蛋白设计：I.氨基酸与野生型氨酰基tRNA合成酶结合的分子对接研究。二。非天然氨基酸掺入的突变型氨酰基-tRNA合成酶的基于结构的设计。
6. Quantitative structure-activity relationship and molecular docking studies of a series of quinazolinonyl analogues as inhibitors of gamma amino butyric acid aminotransferase [O] . Usman Abdulfatai, Adamu Uzairu, Sani Uba 2017

机译：一系列喹唑啉酮类似物作为γ-氨基丁酸氨基转移酶抑制剂的定量构效关系和分子对接研究
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8. Relationships of Quantitative Structure-Activity to Comparative Toxicity of Selected Phenols in the 'Pimephales promelas' and 'Tetrahymena pyriformis' Test Systems [R] . Schultz, T. W. , Holcombe, G. W. , Phipps, G. L. 1986

机译：定位结构 - 活性与'pimephales promelas'和'Tetrahymena pyriformis'试验系统中选定酚的比较毒性的关系

QUANTITATIVE STRUCTURE (INHIBITORY) ACTIVITY RELATIONSHIP AND MOLECULAR DOCKING STUDIES OF PHENOLIC ACIDS TO ANGIOTENSIN-CONVERTINGENZYME

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