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Antibacterial Activity of Salicylanilide 4-(Trifluoromethyl)benzoates

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F13%3A10145614" target="_blank" >RIV/00216208:11160/13:10145614 - isvavai.cz</a>

  • Alternative codes found

    RIV/71009396:_____/13:N0000003

  • Result on the web

    <a href="http://www.mdpi.com/1420-3049/18/4/3674/pdf" target="_blank" >http://www.mdpi.com/1420-3049/18/4/3674/pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/molecules18043674" target="_blank" >10.3390/molecules18043674</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antibacterial Activity of Salicylanilide 4-(Trifluoromethyl)benzoates

  • Original language description

    The development of novel antimicrobial agents represents a timely research topic. Eighteen salicylanilide 4-(trifluoromethyl)benzoates were evaluated against Mycobacterium tuberculosis, M. avium and M. kansasii, eight bacterial strains including methicillin-resistant Staphylococcus aureus (MRSA) and for the inhibition of mycobacterial isocitrate lyase. Some compounds were further screened against drug-resistant M. tuberculosis and for their cytotoxicity. Minimum inhibitory concentrations (MICs) for allmycobacterial strains were within 0.5-32 mu mol/L, with 4-chloro-2-[4-(trifluoromethyl)phenylcarbamoyl] phenyl 4-(trifluoromethyl) benzoate superiority. Grampositive bacteria including MRSA were inhibited with MICs }= 0.49 mu mol/L, while Gram-negative ones were much less susceptible. Salicylanilide 4-(trifluoromethyl) benzoates showed significant antibacterial properties, for many strains being comparable to standard drugs (isoniazid, benzylpenicillin) with no cross-resistance. All este

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Molecules

  • ISSN

    1420-3049

  • e-ISSN

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    15

  • Pages from-to

    3674-3688

  • UT code for WoS article

    000318020100002

  • EID of the result in the Scopus database