首页> 外文OA文献 >Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities

【2h】

Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities

机译：基于结构的设计，合成，分子对接研究和1,2,4-三嗪衍生物作为具有抗氧化活性的COX / 15-LOX抑制剂的1,2,4-三嗪衍生物的生物学评价

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Mehdi Khoshneviszadeh; Omolbanin Shahraki; Mahsima Khoshneviszadeh; Alireza Foroumadi; Omidreza Firuzi; Najmeh Edraki; Hamid Nadri; Alireza Moradi; Abbas Shafiee; Ramin Miri;
展开▼
作者单位

展开▼
年度 2016
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities [J] . Mehdi Khoshneviszadeh, Omolbanin Shahraki, Mahsima Khoshneviszadeh, Journal of enzyme inhibition and medicinal chemistry. . 2016,第6期

机译：基于结构的设计，合成，分子对接研究和1,2,4-三嗪衍生物作为具有抗氧化活性的COX / 15-LOX抑制剂的生物学评估
2. Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities [J] . Khoshneviszadeh Mehdi, Shahraki Omolbanin, Khoshneviszadeh Mahsima, Journal of enzyme inhibition and medicinal chemistry. . 2016,第4a6期

机译：基于结构的设计，合成，分子对接研究和1,2,4-三嗪衍生物作为抗氧化活性的COX / 15-LOX抑制剂的1,2,4-三嗪衍生物的生物学评价
3. Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study. [J] . El Sayed MA, Abdel Aziz NI, Abdel Aziz AA, Bioorganic and medicinal chemistry . 2011,第11期

机译：选择性和吡唑衍生物作为选择性COX-2抑制剂的设计，合成和生物学评估：分子对接研究。
4. Synthesis and Biological Activities of 1,2,4-Triazine Derivatives [C] . TAN Rihong International Conference on Chemical Engineering and Advanced Materials . 2014

机译：1,2,4-三嗪衍生物的合成和生物活性
5. Structure-Based Drug Design in Medicinal Chemistry: I. Development of Translesion Synthesis Inhibitors II. Synthesis and Biological Evaluation of Sulfonyl Piperazine Derivatives for LpxH Inhibition [D] . Lee, Minhee 2017

机译：药物化学中基于结构的药物设计：I.跨病变合成抑制剂的开发II。磺酰哌嗪衍生物对LpxH的抑制作用及其合成及生物学评价
6. Structure-Based Design Synthesis Biological Evaluation and Molecular Docking of Novel PDE10 Inhibitors With Antioxidant Activities [O] . Jinxuan Li, Jing-Yi Chen, Ya-Lin Deng, 2018

机译：具有抗氧化活性的新型PDE10抑制剂的基于结构的设计合成生物学评估和分子对接
7. Novel 9-(alkylthio)-Acenaphtho1,2-e-1,2,4-triazine derivatives: synthesis, cytotoxic activity and molecular docking studies on B-cell lymphoma 2 (Bcl-2) [O] . Mohammad K Mohammadi, Omidreza Firuzi, Mehdi Khoshneviszadeh, 2014

机译：新型9-（烷硫基）-Ac 1,2-e -1,2,4-三嗪衍生物：B细胞淋巴瘤2（Bcl-2）的合成，细胞毒活性和分子对接研究

Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities

著录项

引文网络

相似文献

相关主题

期刊订阅