Molecular Docking Technique for selection of some naproxen derivatives as inhibitors of cyclooxygenase 2 (COX-2)

机译：用于选择一些萘普生衍生物作为环氧氧酶2的抑制剂的分子对接技术（COX-2）

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Molecular Docking Technique has found utility in selecting of naproxen derivatives as inhibitors of cyclooxygenase 2, knowing the fact that naproxen inhibit both forms of cyclooxygenase.

机译：分子对接技术已经发现在选择萘普生衍生物作为环氧化酶2的抑制剂中的效用，知道萘普生抑制两种形式的环氧化酶酶的事实。

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《International Conference on Electronics, Computers and Artificial Intelligence》|2015年||共4页
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Beteringhe Adrian; Symeonidis Flavia Corina Mitroi;
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中图分类自动化技术、计算机技术;
关键词
COX-2; Hex 8.0.; molecular docking; naproxen derivatives;

机译：COX-2;十六进制8.0。;分子对接;萘普生衍生物;

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1. Synthesis, biological evaluation, molecular docking and theoretical evaluation of ADMET properties of nepodin and chrysophanol derivatives as potential cyclooxygenase (COX-1, COX-2) inhibitors [J] . Jagdeep Grover, Vivek Kumar, Vikram Singh, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2014,第Null期

机译：nepodin和chsophophanol衍生物作为潜在的环氧合酶（COX-1，COX-2）抑制剂的ADMET性质的合成，生物学评估，分子对接和理论评估
2. Synthesis, biological evaluation and molecular docking studies of stellatin derivatives as cyclooxygenase (COX-1, COX-2) inhibitors and anti-inflammatory agents. [J] . Gautam R, Jachak SM, Kumar V, Bioorganic and Medicinal Chemistry Letters . 2011,第6期

机译：斯特拉汀衍生物作为环氧氢酶（COX-1，COX-2）抑制剂和抗炎剂的合成，生物学评价和分子对接研究。
3. Computer-Aided Design of Selective COX-2 Inhibitors: Molecular Docking of Structurally Diverse Cyclooxygenase-2 Inhibitors using FlexX Method [J] . Asit K. Chakraborti, Ramasamy Thilagavathi Internet Electronic Journal of Molecular Design . 2003,第2期

机译：选择性COX-2抑制剂的计算机辅助设计：使用FlexX方法对结构多样的环氧合酶2抑制剂进行分子对接
4. Molecular Docking Technique for selection of some naproxen derivatives as inhibitors of cyclooxygenase 2 (COX-2) [C] . Beteringhe Adrian, Symeonidis Flavia Corina Mitroi International Conference on Electronics, Computers and Artificial Intelligence . 2015

机译：用于选择一些萘普生衍生物作为环氧氧酶2的抑制剂的分子对接技术（COX-2）
5. Design, synthesis and biological evaluation of novel tricyclic cyclooxygenase-2 (COX-2) inhibitors. [D] . Perampalli Nekkar, Praveen Rao. 2004

机译：新型三环环氧合酶2（COX-2）抑制剂的设计，合成和生物学评估。
6. Pharmacophore Elucidation and Molecular Docking Studies on 5-Phenyl-1-(3-pyridyl)-1H-124-triazole-3-carboxylic Acid Derivatives as COX-2 Inhibitors [O] . Marc Lindner, Wolfgang Sippl, Awwad A. Radwan 2010

机译：5-苯基-1-（3-吡啶基）-1H-124-三唑-3-羧酸衍生物作为COX-2抑制剂的药理学阐明和分子对接研究
7. Pharmacophore Elucidation and Molecular Docking Studies on 5-Phenyl-1-(3-pyridyl)-1H-1,2,4-triazole-3-carboxylic Acid Derivatives as COX-2 Inhibitors [O] . Lindner, Marc, Sippl, Wolfgang, Radwan, Awwad A. 2010

机译：5-苯基-1-（3-吡啶基）-1H-1,2,4-三唑-3-羧酸衍生物作为COX-2抑制剂的药理学阐明和分子对接研究

Molecular Docking Technique for selection of some naproxen derivatives as inhibitors of cyclooxygenase 2 (COX-2)

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