Design, synthesis and biological activity of novel demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis-Reference-Cited by-同舟云学术

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Design, synthesis and biological activity of novel demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis

Published:2018-07 Issue:27 Volume:74 Page:3527-3533
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Jiang Yong-Wei,Xu Liang,Fu Wei,Lin Hua,Yu Jian-Ming,Sun Xun

Funder

National Natural Science Foundation of China

Science and Technology Developing Foundation of Shanghai

Shanghai Municipal Committee of Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Characterization of the Peptidoglycan of Vancomycin-Susceptible Enterococcus faecium

2. Structure, biochemistry and mechanism of action of glycopeptide antibiotics

3. Molecular mechanisms that confer antibacterial drug resistance

4. A fluorescent ligand for binding studies with glycopeptide antibiotics of the vancomycin class

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1. Synthesis and Antibacterial Evaluation of Novel Vancomycin Derivatives Containing Quaternary Ammonium Moieties;ACS Omega;2023-07-25

2. Synthesis of vancomycin fluorescent probes that retain antimicrobial activity, identify Gram-positive bacteria, and detect Gram-negative outer membrane damage;Communications Biology;2023-04-14

3. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against ESKAPE pathogens;EUR J MED CHEM;2022

4. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against ESKAPE pathogens;European Journal of Medicinal Chemistry;2022-12

5. Recent advances in medicinal chemistry of ampicillin: Derivatives, metal complexes, and sensing approaches;TrAC Trends in Analytical Chemistry;2022-10

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