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1.
Chembiochem ; 18(16): 1573-1577, 2017 08 17.
Artículo en Inglés | MEDLINE | ID: mdl-28510317

RESUMEN

Quaternary ammonium compounds (QACs) are commonly used antiseptics that are now known to be subject to bacterial resistance. The prevalence and mechanisms of such resistance, however, remain underexplored. We investigated a variety of QACs, including those with multicationic structures (multiQACs), and the resistance displayed by a variety of Staphylococcus aureus strains with and without genes encoding efflux pumps, the purported main driver of bacterial resistance in MRSA. Through minimum inhibitory concentration (MIC)-, kinetic-, and efflux-based assays, we found that neither the qacR/qacA system present in S. aureus nor another efflux pump system is the main reason for bacterial resistance to QACs. Our findings suggest that membrane composition could be the predominant driver that allows CA-MRSA to withstand the assault of conventional QAC antiseptics.


Asunto(s)
Antiinfecciosos Locales/farmacocinética , Compuestos de Benzalconio/farmacocinética , Farmacorresistencia Bacteriana Múltiple/efectos de los fármacos , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Antiinfecciosos Locales/farmacología , Proteínas Bacterianas/genética , Compuestos de Benzalconio/farmacología , Carbonil Cianuro m-Clorofenil Hidrazona/farmacología , Permeabilidad de la Membrana Celular , Moduladores del Transporte de Membrana/farmacología , Proteínas de Transporte de Membrana/genética , Staphylococcus aureus Resistente a Meticilina/clasificación , Pruebas de Sensibilidad Microbiana , Proteínas Represoras/genética , Reserpina/farmacología , Desacopladores/farmacología
2.
ChemMedChem ; 15(22): 2151-2156, 2020 11 18.
Artículo en Inglés | MEDLINE | ID: mdl-32729197

RESUMEN

Adenosine deaminase (ADA) is a human mononuclear Zn2+ metalloenzyme that converts adenosine to inosine. ADA is a validated drug target for cancer, but there has been little recent work on the development of new therapeutics against this enzyme. The lack of new advancements can be partially attributed to an absence of suitable assays for high-throughput screening (HTS) against ADA. To facilitate more rapid drug discovery efforts for this target, an in vitro assay was developed that utilizes the enzymatic conversion of a visibly emitting adenosine analogue to the corresponding fluorescent inosine analogue by ADA, which can be monitored via fluorescence intensity changes. Utilizing this assay, a library of ∼350 small molecules containing metal-binding pharmacophores (MBPs) was screened in an HTS format to identify new inhibitor scaffolds against ADA. This approach yielded a new metal-binding scaffold with a Ki value of 26±1 µM.


Asunto(s)
Inhibidores de la Adenosina Desaminasa/farmacología , Adenosina Desaminasa/metabolismo , Oxazoles/farmacología , Zinc/farmacología , Inhibidores de la Adenosina Desaminasa/síntesis química , Inhibidores de la Adenosina Desaminasa/química , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Humanos , Estructura Molecular , Oxazoles/química , Zinc/química
4.
ChemMedChem ; 12(23): 1931-1934, 2017 12 07.
Artículo en Inglés | MEDLINE | ID: mdl-29068517

RESUMEN

Benzalkonium chloride (BAC) and cetyl pyridinium chloride (CPC) are two of the most common household antiseptics, but show weaker efficacy against Gram-negative bacteria as well as against methicillin-resistant Staphylococcus aureus (MRSA) strains, relative to other S. aureus strains. We prepared 28 novel quaternary ammonium compounds (QACs) that represent a hybrid of these two structures, using 1- to 2-step synthetic sequences. The biscationic (bisQAC) species prepared show uniformly potent activity against six bacterial strains tested, with nine novel antiseptics displaying single-digit micromolar activity across the board. Effects of unequal chain lengths of two installed side chains had less impact than the overall number of side chain carbon atoms present, which was optimal at 22-25 carbons. This is further indication that simple refinements to multiQAC architectures can show improvement over current household antiseptics.


Asunto(s)
Antiinfecciosos Locales/farmacología , Bacterias/efectos de los fármacos , Compuestos de Amonio Cuaternario/farmacología , Antiinfecciosos Locales/síntesis química , Antiinfecciosos Locales/química , Compuestos de Benzalconio/química , Compuestos de Benzalconio/farmacología , Cationes/síntesis química , Cationes/química , Cationes/farmacología , Cetilpiridinio/química , Cetilpiridinio/farmacología , Relación Dosis-Respuesta a Droga , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Compuestos de Amonio Cuaternario/síntesis química , Compuestos de Amonio Cuaternario/química
5.
ChemMedChem ; 11(9): 958-62, 2016 05 06.
Artículo en Inglés | MEDLINE | ID: mdl-27027389

RESUMEN

Bacterial resistance toward commonly used biocides is a widespread yet underappreciated problem, one which needs not only a deeper understanding of the mechanisms by which resistance proliferates, but also means for mitigation. To advance our understanding of this issue, we recognized a polyaromatic structural core analogous to activators of QacR, a negative transcriptional regulator of the efflux pump QacA, and envisioned a series of quaternary ammonium compounds (QACs) based on this motif. Using commercially available dye scaffolds, we synthesized and evaluated the antimicrobial activity of 52 novel QACs bearing 1-3 quaternary ammonium centers. Striking differences in antimicrobial activity against bacteria bearing QAC resistance genes have been observed, with up to a 125-fold increase in minimum inhibitory concentration (MIC) for select structures against bacteria known to bear efflux pumps. Based on these findings, general trends in structure-resistance relationships have been identified, laying the groundwork for future mechanistic studies.


Asunto(s)
Antibacterianos/farmacología , Bacterias/efectos de los fármacos , Colorantes/química , Farmacorresistencia Bacteriana/efectos de los fármacos , Compuestos de Amonio Cuaternario/química , Antibacterianos/síntesis química , Antibacterianos/química , Proteínas Bacterianas/metabolismo , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Compuestos de Amonio Cuaternario/síntesis química , Compuestos de Amonio Cuaternario/farmacología , Relación Estructura-Actividad
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