Towards understanding the mechanism of action of antibacterial N-alkyl-3-hydroxypyridinium salts: Biological activities, molecular modeling and QSAR studies
Language English Country France Media print-electronic
Document type Journal Article
PubMed
27341309
DOI
10.1016/j.ejmech.2016.05.058
PII: S0223-5234(16)30456-1
Knihovny.cz E-resources
- Keywords
- Antimicrobials, Molecular dynamics, Molecular modeling, QSAR, Quaternary ammoniums salts, Surfactants,
- MeSH
- Anti-Bacterial Agents chemistry pharmacology toxicity MeSH
- Bacteria drug effects MeSH
- CHO Cells MeSH
- Cricetulus MeSH
- Fungi drug effects MeSH
- Hydrophobic and Hydrophilic Interactions MeSH
- Cricetinae MeSH
- Quantitative Structure-Activity Relationship * MeSH
- Molecular Conformation MeSH
- Pyridines chemistry pharmacology toxicity MeSH
- Molecular Dynamics Simulation * MeSH
- Cell Survival drug effects MeSH
- Animals MeSH
- Check Tag
- Cricetinae MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 3-hydroxypyridine MeSH Browser
- Anti-Bacterial Agents MeSH
- Pyridines MeSH
In this study, we have carried out a combined experimental and computational investigation to elucidate several bred-in-the-bone ideas standing out in rational design of novel cationic surfactants as antibacterial agents. Five 3-hydroxypyridinium salts differing in the length of N-alkyl side chain have been synthesized, analyzed by high performance liquid chromatography, tested for in vitro activity against a panel of pathogenic bacterial and fungal strains, computationally modeled in water by a SCRF B3LYP/6-311++G(d,p) method, and evaluated by a systematic QSAR analysis. Given the results of this work, the hypothesis suggesting that higher positive charge of the quaternary nitrogen should increase antimicrobial efficacy can be rejected since 3-hydroxyl group does increase the positive charge on the nitrogen but, simultaneously, it significantly derogates the antimicrobial activity by lowering the lipophilicity and by escalating the desolvation energy of the compounds in comparison with non-hydroxylated analogues. Herein, the majority of the prepared 3-hydroxylated substances showed notably lower potency than the parent pyridinium structures, although compound 8 with C12 alkyl chain proved a distinctly better antimicrobial activity in submicromolar range. Focusing on this anomaly, we have made an effort to reveal the reason of the observed activity through a molecular dynamics simulation of the interaction between the bacterial membrane and compound 8 in GROMACS software.
References provided by Crossref.org
Carltonine-derived compounds for targeted butyrylcholinesterase inhibition
Synthesis and Decontamination Effect on Chemical and Biological Agents of Benzoxonium-Like Salts
The Antibacterial Effects of New N-Alkylpyridinium Salts on Planktonic and Biofilm Bacteria
Wide-Antimicrobial Spectrum of Picolinium Salts