Synthesis and biological evaluation of a MraY selective analogue of tunicamycins-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of a MraY selective analogue of tunicamycins

Published:2019-09-30 Issue:1-3 Volume:39 Page:349-364
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Yamamoto Kazuki¹,Sato Toyotaka²,Hikiji Yuta¹,Katsuyama Akira¹³,Matsumaru Takanori¹³,Yakushiji Fumika¹³,Yokota Shin-Ichi²,Ichikawa Satoshi¹³

Affiliation:

1. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan;

2. Department of Microbiology, Sapporo Medical University School of Medicine, Sapporo, Japan;

3. Center for Research and Education on Drug Discovery, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2019.1649696

Reference36 articles.

1. Topological analysis of the MraY protein catalysing the first membrane step of peptidoglycan synthesis

2. The biosynthesis of peptidoglycan lipid-linked intermediates

3. Active Site Mapping of MraY, a Member of the Polyprenyl-phosphate N-Acetylhexosamine 1-Phosphate Transferase Superfamily, Catalyzing the First Membrane Step of Peptidoglycan Biosynthesis

4. Recent advances in antimicrobial nucleoside antibiotics targeting cell wall biosynthesis

5. Phospho-MurNAc-Pentapeptide Translocase (MraY) as a Target for Antibacterial Agents and Antibacterial Proteins

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1. Nucleoside-derived inhibitors of MraY: Medicinal chemistry with natural products;New Approaches Towards Novel Antibacterial Agents;2023

2. Synthesis of chimera oligopeptide including furanoid β-sugar amino acid derivatives with free OHs: mild but successful removal of the 1,2-O-isopropylidene from the building block;Amino Acids;2021-02

3. Uridine natural products: Challenging targets and inspiration for novel small molecule inhibitors;Bioorganic & Medicinal Chemistry;2020-09

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