Compounds > vancomycin
Page last updated: 2024-08-21

vancomycin and cetrimonium bromide

vancomycin has been researched along with cetrimonium bromide in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (80.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Chan, KY; Chang, CW; Litke, AP; Redman, N; Zeng, J; Zhan, J; Zhang, J1
Bartůněk, P; Bogdanová, K; Kolář, M; Kovačková, S; Krásný, L; Látal, T; Nyč, O; Pohl, R; Pombinho, AR; Rabatinová, A; Rejman, D; Sanderová, H; Zborníková, E1
Attene-Ramos, M; Baker, HL; Burkart, MD; Daniel, T; Foley, TL; Jadhav, A; Kosa, NM; Leister, W; Maloney, DJ; Rai, G; Simeonov, A; Yasgar, A1
Beniddir, MA; Bernadat, G; Fontaine, V; Fouotsa, H; Gallard, JF; Lannang, AM; Le Pogam, P; Leblanc, K; Meyer, F; Mkounga, P; Nkengfack, AE; Poupon, E; Rharrabti, S; Vanheuverzwijn, J; Zhou, Z1

Other Studies

5 other study(ies) available for vancomycin and cetrimonium bromide

ArticleYear
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Synthesis and antibacterial activity study of a novel class of cationic anthraquinone analogs.
    Bioorganic & medicinal chemistry, 2011, Jan-01, Volume: 19, Issue:1

    Topics: Anthraquinones; Anti-Bacterial Agents; Cations; Magnetic Resonance Spectroscopy; Microbial Sensitivity Tests; Spectrometry, Mass, Electrospray Ionization

2011
Lipophosphonoxins: new modular molecular structures with significant antibacterial properties.
    Journal of medicinal chemistry, 2011, Nov-24, Volume: 54, Issue:22

    Topics: Anti-Bacterial Agents; Apoptosis; Cell Survival; Cells, Cultured; Drug Resistance, Multiple, Bacterial; Erythroid Precursor Cells; Fetal Blood; Gram-Positive Bacteria; Humans; Hydrophobic and Hydrophilic Interactions; Microbial Sensitivity Tests; Nucleosides; Organophosphonates; Stereoisomerism; Structure-Activity Relationship

2011
4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide (ML267), a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth.
    Journal of medicinal chemistry, 2014, Feb-13, Volume: 57, Issue:3

    Topics: Animals; Anti-Bacterial Agents; Bacterial Proteins; Dipeptides; Drug Resistance, Bacterial; Drug Synergism; Escherichia coli; Gram-Positive Bacteria; Humans; Male; Mice; Microbial Sensitivity Tests; Microsomes, Liver; Pyridines; Secondary Metabolism; Structure-Activity Relationship; Thiourea; Transferases (Other Substituted Phosphate Groups)

2014
Voatriafricanines A and B, Trimeric Vobasine-Aspidosperma-Aspidosperma Alkaloids from
    Journal of natural products, 2021, 10-22, Volume: 84, Issue:10

    Topics: Anti-Bacterial Agents; Cameroon; Indole Alkaloids; Molecular Structure; Phytochemicals; Plant Bark; Voacanga

2021