首页> 美国卫生研究院文献>BMC Chemistry >In silico design and synthesis of hesperitin derivatives as new xanthine oxidase inhibitors

【2h】

In silico design and synthesis of hesperitin derivatives as new xanthine oxidase inhibitors

机译：在计算机上设计和合成橙皮素衍生物作为新的黄嘌呤氧化酶抑制剂

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

摘要
著录项
引文网络
相似文献
相关主题

摘要

BackgroundHesperitin, a naturally occurring flavonoid was hybridized with phenolic acids to evaluate its potential to inhibit the activity of xanthine oxidase (XO), a key enzyme which catalyses xanthine to uric acid which is found to be associated with gout and many life style related disorders.

机译：背景橙皮素（一种天然存在的类黄酮）与酚酸杂交，以评估其抑制黄嘌呤氧化酶（XO）活性的潜力。

著录项

期刊名称 BMC Chemistry
作者
Neelam Malik; Priyanka Dhiman; Anurag Khatkar;
展开▼
作者单位

展开▼
年(卷),期 2019(13),1
年度 2019
页码 53
总页数 11
原文格式 PDF
正文语种
中图分类生化遗传学;生化药理学;
关键词
Hesperitin Xanthine oxidase Molecular docking Antioxidant;

机译：橙皮素;黄嘌呤氧化酶;分子对接;抗氧化剂;

相似文献

外文文献
中文文献
专利

1. In silico design and synthesis of hesperitin derivatives as new xanthine oxidase inhibitors [J] . Neelam Malik, Priyanka Dhiman, Anurag Khatkar Chemistry central journal . 2019,第1期

机译：在计算机上设计和合成橙皮素衍生物作为新的黄嘌呤氧化酶抑制剂
2. In silico design and synthesis of targeted rutin derivatives as xanthine oxidase inhibitors [J] . Neelam Malik, Priyanka Dhiman, Anurag Khatkar Chemistry central journal . 2019,第1期

机译：在计算机上设计和合成作为黄嘌呤氧化酶抑制剂的靶向芦丁衍生物
3. In Silico Design and Synthesis of Targeted Curcumin Derivatives as Xanthine Oxidase Inhibitors [J] . Malik Neelam, Dhiman Priyanka, Khatkar Anurag Current drug targets-The International journal for timely in-depth reviews on drug targets . 2019,第5期

机译：在硅的设计和合成靶向姜黄素衍生物中作为黄嘌呤氧化酶抑制剂
4. Molecular docking analysis of imidazole derivatives and polybenzimidazole analogs as inhibitors of superoxide dismutase (SOD) and xanthine oxidase (XO) [C] . Vijayakumar Veeraragavan, Radhakrishnan Narayanaswamy, Rameshkumar Chidambaram 2017 IEEE International Conference on Smart Technologies and Management for Computing, Communication, Controls, Energy and Materials . 2017

机译：咪唑衍生物和聚苯并咪唑类似物作为超氧化物歧化酶（SOD）和黄嘌呤氧化酶（XO）抑制剂的分子对接分析
5. Part One. Synthesis of optically active tryptophan derivatives with potential activity as indoleamine 2,3-dioxygenase inhibitors: An approach via asymmetric catalytic hydrogenation. Part Two. Design, synthesis and pharmacology of selective ligands for alpha1-containing GABA(A)/benzodiazepine receptor subtypes: SAR studies of beta-carbolines at positions -3 and -6 and their corresponding bivalent ligands. Part Three. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. [D] . Yin, Wenyuan. 2007

机译：第一部分。具有吲哚胺2,3-二加氧酶抑制剂潜在活性的旋光色氨酸衍生物的合成：一种通过不对称催化氢化的方法。第二部分。含α1的GABA（A）/苯并二氮杂receptor受体亚型的选择性配体的设计，合成和药理作用：位于-3和-6位的β-咔啉及其相应的二价配体的SAR研究。第三部分。重要生物遗传中间体，（+）-聚神经氨酸和（+）-聚神经氨酸醛，以及16-表-维西辛和Macusine A的首次对映体全合成。
6. In silico design and synthesis of targeted rutin derivatives as xanthine oxidase inhibitors [O] . Neelam Malik, Priyanka Dhiman, Anurag Khatkar 2019

机译：在计算机上设计和合成作为黄嘌呤氧化酶抑制剂的靶向芦丁衍生物
7. In silico design and synthesis of hesperitin derivatives as new xanthine oxidase inhibitors [O] . Neelam Malik, Priyanka Dhiman, Anurag Khatkar 2019

机译：在硅的设计和合成Herperitin衍生物作为新的黄嘌呤氧化酶抑制剂

In silico design and synthesis of hesperitin derivatives as new xanthine oxidase inhibitors

摘要

著录项

引文网络

相似文献

相关主题

期刊订阅