One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria.

Moraski GC; Podos SD; Miller MJ

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One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria.

机译：硝基呋喃基苯并咪唑的一步合成，其对多药抗性细菌有效。

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摘要

Nitrofuranyl benzimidazoles can be made in one synthetic step from commercially available starting materials. The compounds displayed unexpected antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci with MICs as low as 1 mug ml(-1).

机译：硝基呋喃基苯并咪唑可以从市售原料中的一个合成步骤中制成。该化合物显示出对耐甲氧西林耐金黄色葡萄球菌（MRSA）的意外抗菌活性，并且具有低至1张甲甲克（-1）的MICS的万古霉素抗性肠球菌。

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《The Journal of Antibiotics: An International Journal》 |2011年第10期|共5页
作者
Moraski GC; Podos SD; Miller MJ;
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Department of Chemistry and Biochemistry University of Notre Dame Notre Dame IN USA.;

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原文格式 PDF
正文语种 eng
中图分类药学;
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1. One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria. [J] . Moraski GC, Podos SD, Miller MJ The Journal of Antibiotics: An International Journal . 2011,第10期

机译：对多药耐药细菌具有活性的硝基呋喃基苯并咪唑的一步合成。
2. One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria. [J] . Moraski GC, Podos SD, Miller MJ The Journal of Antibiotics: An International Journal . 2011,第10期

机译：硝基呋喃基苯并咪唑的一步合成，其对多药抗性细菌有效。
3. One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria. [J] . Moraski GC, Podos SD, Miller MJ The Journal of Antibiotics: An International Journal . 2011,第10期

机译：硝基呋喃基苯并咪唑的一步合成，其对多药抗性细菌有效。
4. Syntheses, Crystal Structures and Luminescence of Two Coordination Polymers Based on Isophthalic Acid and 2-(3-Pyridyl)benzimidazole Ligands [C] . Kefen Yue, Shuang Zhao, Ruili Zhao International Conference on Chemical, Material and Metallurgical Engineering . 2012

机译：基于间苯二甲酸和2-（3-吡啶基）苯并咪唑配体的两种配位聚合物的合成，晶体结构和发光
5. Development of a vinylogous Horner-Wadsworth-Emmons reagent: Syntheses of siloxy dienes, aryl amines and medicinally active compounds. [D] . Markiewicz, John T. 2011

机译：乙烯基霍纳-沃兹沃斯-埃蒙斯试剂的开发：甲硅烷氧基二烯，芳基胺和药用活性化合物的合成。
6. One Step Syntheses of Nitrofuranyl Benzimidazoles that are Active Against Multi-Drug Resistant Bacteria [O] . Garrett C. Moraski, Jane A. Thanassi, Steven D. Podos, -1

机译：硝基呋喃基苯并咪唑的一步合成其具有针对多药物抗性细菌的活性
7. One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria [O] . Garrett C Moraski, Jane A Thanassi, Steven D Podos, 2011

机译：硝基呋喃基苯并咪唑的一步合成，其对抗多药细菌有效
8. Syntheses of Diaza-18-Crown-6 Ligands Containing Two Units Each of 4-Hydroxyazobenzene, Benzimidazole, Uracil, Anthraquinone, or Ferrocene Groups [R] . Su, N. , Bradshaw, J. S. , Zhang, X. X. , 1999

机译：含有两个单元的二氮杂-18-冠-6配体的合成4-羟基偶氮苯，苯并咪唑，尿嘧啶，蒽醌或二茂铁基团

One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria.

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