Page last updated: 2024-08-17

salicylanilide and carbamates

salicylanilide has been researched along with carbamates in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Férriz, JM; Imramovský, A; Kunc, F; Stolaríková, J; Vavríková, E; Vávrová, K; Vinsová, J1
Ferriz, JM; Imramovsky, A; Jampilek, J; Kralova, K; Pesko, M; Vinsova, J1
Imramovsky, A; Jampilek, J; Monreal-Ferriz, J; Pauk, K; Stepankova, S; Vanco, J; Vinsova, J1
Krátký, M; Novotná, E; Stolaříková, J; Trejtnar, F; Vinšová, J; Volková, M1
Baranyai, Z; Bősze, S; Dávid, S; Horváti, K; Krátký, M; Senoner, Z; Stolaříková, J; Szabó, N; Vinšová, J1
Baranyai, Z; Bősze, S; Janďourek, O; Krátký, M; Novotná, E; Stolaříková, J; Vinšová, J1

Other Studies

6 other study(ies) available for salicylanilide and carbamates

ArticleYear
Salicylanilide carbamates: antitubercular agents active against multidrug-resistant Mycobacterium tuberculosis strains.
    Bioorganic & medicinal chemistry, 2010, Volume: 18, Issue:3

    Topics: Antitubercular Agents; Carbamates; Cell Line; Cell Proliferation; Humans; Mycobacterium tuberculosis; Salicylanilides; Tuberculosis

2010
Photosynthesis-Inhibiting efficiency of 4-chloro-2-(chlorophenylcarbamoyl)phenyl alkylcarbamates.
    Bioorganic & medicinal chemistry letters, 2011, Aug-01, Volume: 21, Issue:15

    Topics: Carbamates; Photosynthesis; Photosynthetic Reaction Center Complex Proteins; Salicylanilides; Spinacia oleracea; Structure-Activity Relationship

2011
Acetylcholinesterase-inhibiting activity of salicylanilide N-alkylcarbamates and their molecular docking.
    Molecules (Basel, Switzerland), 2012, Aug-24, Volume: 17, Issue:9

    Topics: Acetylcholinesterase; Animals; Binding Sites; Carbamates; Catalytic Domain; Cholinesterase Inhibitors; Electrophorus; Galantamine; Models, Molecular; Molecular Docking Simulation; Phenylcarbamates; Rivastigmine; Salicylanilides; Structure-Activity Relationship

2012
Synthesis and biological activity of new salicylanilide N,N-disubstituted carbamates and thiocarbamates.
    Bioorganic & medicinal chemistry, 2014, Aug-01, Volume: 22, Issue:15

    Topics: Anti-Infective Agents; Carbamates; Cell Survival; Fungi; Gram-Positive Bacteria; Hep G2 Cells; Humans; Isocitrate Lyase; Methicillin-Resistant Staphylococcus aureus; Microbial Sensitivity Tests; Mycobacterium avium; Mycobacterium kansasii; Salicylanilides; Structure-Activity Relationship; Thiocarbamates

2014
Combating highly resistant emerging pathogen Mycobacterium abscessus and Mycobacterium tuberculosis with novel salicylanilide esters and carbamates.
    European journal of medicinal chemistry, 2015, Aug-28, Volume: 101

    Topics: Anti-Bacterial Agents; Carbamates; Cell Line; Dose-Response Relationship, Drug; Esters; Humans; Microbial Sensitivity Tests; Molecular Structure; Mycobacterium; Salicylanilides; Structure-Activity Relationship; Tuberculosis, Multidrug-Resistant

2015
Phenolic N-monosubstituted carbamates: Antitubercular and toxicity evaluation of multi-targeting compounds.
    European journal of medicinal chemistry, 2019, Nov-01, Volume: 181

    Topics: Antitubercular Agents; Carbamates; Hep G2 Cells; Humans; Isocitrate Lyase; Mycobacterium tuberculosis; Phenols; Salicylanilides; Tuberculosis

2019