Synthesis and biological evaluation of a MraY selective analogue of tunicamycins.
Anti-Bacterial Agents
/ chemical synthesis
Bacterial Proteins
/ antagonists & inhibitors
Cell Line
Chemistry Techniques, Synthetic
Humans
Models, Molecular
Molecular Conformation
Molecular Structure
Structure-Activity Relationship
Transferases
/ antagonists & inhibitors
Transferases (Other Substituted Phosphate Groups)
Tunicamycin
/ chemical synthesis
antibacterial
nucleoside natural products
organic chemistry
Journal
Nucleosides, nucleotides & nucleic acids
ISSN: 1532-2335
Titre abrégé: Nucleosides Nucleotides Nucleic Acids
Pays: United States
ID NLM: 100892832
Informations de publication
Date de publication:
2020
2020
Historique:
pubmed:
1
10
2019
medline:
23
9
2020
entrez:
1
10
2019
Statut:
ppublish
Résumé
Tunicamycins, which are nucleoside natural products, inhibit both bacterial phospho-
Identifiants
pubmed: 31566068
doi: 10.1080/15257770.2019.1649696
doi:
Substances chimiques
Anti-Bacterial Agents
0
Bacterial Proteins
0
Tunicamycin
11089-65-9
Transferases
EC 2.-
Transferases (Other Substituted Phosphate Groups)
EC 2.7.8.-
mraY protein, Bacteria
EC 2.7.8.13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM