1,2,3-Triazole‑gold(I)-triethylphosphine derivatives of nutrients as new antimicrobials against antibiotic resistant Gram-positive pathogens

The ongoing rise of bacterial resistance against antibiotics is an incentive to develop radically new antibacterial molecules. Innovative organo-gold(I) antibacterial compounds were synthesized by click chemistry with triethylphosphine‑gold(I) azides and alkyne-functionalized metabolites like amino acids, nicotinic acid and biotin. The resulting organo‑gold(I) compounds exhibited remarkable activities against a panel of Gram-positive pathogens (Staphyloccocus sp., Enterococcus sp. and Clostridium difficile) but failed to inhibit the growth of Gram-negative bacilli (e.g., Escherichia coli) under the conditions used (8 μg. mL<sup>-1</sup> maximum).

Authors

Institutions

Publication Details

Journal
Bioorganic & Medicinal Chemistry Letters
Published
2025-05-14
DOI
https://doi.org/10.1016/j.bmcl.2025.130276
Citations
1
Primary Topic
Metal complexes synthesis and properties
Type
article
Field-Weighted Citation Impact
1.05

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

1,2,3-Triazole‑gold(I)-triethylphosphine derivatives of nutrients as new antimicrobials against antibiotic resistant Gram-positive pathogens

Gaëtan L. A. Mislin, Alexandre Steffen, Mathieu Michaut, Françoise Hoegy et al.
1 citations
Bioorganic & Medicinal Chemistry Letters
Metal complexes synthesis and properties
1.05
article

1,2,3-Triazole‑gold(I)-triethylphosphine derivatives of nutrients as new antimicrobials against antibiotic resistant Gram-positive pathogens

Gaëtan L. A. Mislin, Alexandre Steffen, Mathieu Michaut, Françoise Hoegy, Christophe Morice, Jean‐Marie Contreras, Patrick Plésiat
article en
1 citations

Abstract

The ongoing rise of bacterial resistance against antibiotics is an incentive to develop radically new antibacterial molecules. Innovative organo-gold(I) antibacterial compounds were synthesized by click chemistry with triethylphosphine‑gold(I) azides and alkyne-functionalized metabolites like amino acids, nicotinic acid and biotin. The resulting organo‑gold(I) compounds exhibited remarkable activities against a panel of Gram-positive pathogens (Staphyloccocus sp., Enterococcus sp. and Clostridium difficile) but failed to inhibit the growth of Gram-negative bacilli (e.g., Escherichia coli) under the conditions used (8 μg. mL<sup>-1</sup> maximum).

Bioorganic & Medicinal Chemistry LettersVol. 125-126
Centre National de la Recherche Scientifique (FR), Laboratoire Chrono-Environnement (FR), Biotechnologie et Signalisation Cellulaire (FR)
Agence Nationale de la Recherche, Centre National de la Recherche Scientifique
Zero hunger
Openalex Percentile: Top 22%
Metal complexes synthesis and properties
1.05
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.