1,3,5-Triazine as Branching Connector for the Construction of Novel Antimicrobial Peptide Dendrimers: Synthesis and Biological Characterization.
2,4,6-Trichloro-1,3,5-triazine (TCT)
antimicrobials
efflux pump inhibitors
multidrug-resistant bacteria (MDR)
peptide dendrimers
solid-phase peptide synthesis (SPPS)
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
28 May 2024
28 May 2024
Historique:
received:
24
04
2024
revised:
21
05
2024
accepted:
24
05
2024
medline:
19
6
2024
pubmed:
19
6
2024
entrez:
19
6
2024
Statut:
epublish
Résumé
Peptides displaying antimicrobial properties are being regarded as useful tools to evade and combat antimicrobial resistance, a major public health challenge. Here we have addressed dendrimers, attractive molecules in pharmaceutical innovation and development displaying broad biological activity. Triazine-based dendrimers were fully synthesized in the solid phase, and their antimicrobial activity and some insights into their mechanisms of action were explored. Triazine is present in a large number of compounds with highly diverse biological targets with broad biological activities and could be an excellent branching unit to accommodate peptides. Our results show that the novel peptide dendrimers synthesized have remarkable antimicrobial activity against Gram-negative bacteria (
Identifiants
pubmed: 38892071
pii: ijms25115883
doi: 10.3390/ijms25115883
pii:
doi:
Substances chimiques
Dendrimers
0
Triazines
0
Antimicrobial Peptides
0
Anti-Bacterial Agents
0
Anti-Infective Agents
0
Antimicrobial Cationic Peptides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Marato TV3
ID : BARNAPA 201/C/2018
Organisme : National Research Foundation
ID : Blue Sky's Research program 120386