首页> 外文OA文献 >Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis

【2h】

Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis

机译：核苷前药的合成与药理学评价，旨在靶向结核分枝杆菌杆菌生物合成的

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
Surendra Dawadi; Shuhei Kawamura; Anja Rubenstein; Rory Remmel; Courtney C. Aldrich;
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. Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis [J] . Dawadi Surendra, Kawamura Shuhei, Rubenstein Anja, Bioorganic and medicinal chemistry . 2016,第6期

机译：靶向结核分枝杆菌中铁载体生物合成的核苷前药的合成和药理评价
2. Rationally Designed Nucleoside Antibiotics That Inhibit Siderophore Biosynthesis of Mycobacterium tuberculosis [J] . Ravindranadh V.Somu, Helena Boshoff, Chunhua Qiao, Journal of Medicinal Chemistry . 2006,第1期

机译：合理设计的抑制结核分枝杆菌铁载体生物合成的核苷类抗生素
3. 2-Aryl-8-aza-3-deazaadenosine analogues of 5 '-O-[N-(salicyl)sulfamoyl]adenosine: Nucleoside antibiotics that block siderophore biosynthesis in Mycobacterium tuberculosis [J] . Krajczyk Anna, Zeidler Joanna, Januszczyk Piotr, Bioorganic and medicinal chemistry . 2016,第14a15期

机译：2- aryl-8-aza-3-deazaadenosine类似物为5'-o- [n-（水杨酸）sulfamoyl]腺苷：核苷抗生素，阻止曾结核分枝杆菌中的二氧化碳生物合成
4. Biosynthesis of the Thiolactone Derivative of Enterococcus faecalis Gelatinase-Biosynthesis Activating Pheromone by using the Mycobacterium xenopi GyrA Mini-Intein [C] . Yosuke Yamanaka, Kou Hayakawa, Hidekazu Katayama Japanese peptide symposium . 2010

机译：肠球菌粪便蛋白甲状腺素衍生物的生物合成通过使用Xenopi Gyra Mini-Intein激活信息素激活信息素
5. Design, synthesis and biological evaluation of glutathione peptidomimetics as components of targeted prodrugs and glyoxalase I inhibitors [D] . More, Swati Sudhakar 2007

机译：谷胱甘肽模拟肽作为靶向前药和乙二醛酶I抑制剂的组成成分的设计，合成和生物学评估
6. Synthesis and Pharmacological Evaluation of Nucleoside Prodrugs Designed to Target Siderophore Biosynthesis in Mycobacterium tuberculosis [O] . Surendra Dawadi, Shuhei Kawamura, Anja Rubenstein, -1

机译：靶向结核分枝杆菌生物合成的核苷类前药的合成及药理评价
7. Rationally Designed Nucleoside Antibiotics That Inhibit Siderophore Biosynthesis of Mycobacterium tuberculosis [O] . -1

机译：理性设计的核苷抗生素，抑制结核分枝杆菌的纵向细胞生物合成

Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis

著录项

引文网络

相似文献

相关主题

期刊订阅