The in vitro antimycobacterial investigation of some basic meta-/para-alkoxyphenylcarbamic esters bearing 4-(4-Fluoro/2-methoxyphenyl)piperazin-1-yl fragment

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F13%3A43872458" target="_blank" >RIV/62157124:16370/13:43872458 - isvavai.cz</a>
Alternative codes found
RIV/62157124:16370/13:43872463
Result on the web
<a href="http://dx.doi.org/10.3329/dujps.v12i2.17621" target="_blank" >http://dx.doi.org/10.3329/dujps.v12i2.17621</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3329/dujps.v12i2.17621" target="_blank" >10.3329/dujps.v12i2.17621</a>

Result language
angličtina
Original language name
The in vitro antimycobacterial investigation of some basic meta-/para-alkoxyphenylcarbamic esters bearing 4-(4-Fluoro/2-methoxyphenyl)piperazin-1-yl fragment
Original language description
Following previous systematical research of ortho-/meta-/para-alkoxyphenylcarbamic acid esters as antimycobacterially active compounds, the set of the derivatives containing meta-/para-alkoxyphenylcarbamoyloxy and 4-(4-fluorophenyl/2-methoxyphenyl)piperazin-1-yl moieties were tested for their in vitro activity against tuberculous strain of Mycobacterium (M.) tuberculosis CNCTC My 331/88 as well as against potential pathogenic strains of M. kansasii CNCTC My 235/80, M. avium CNCTC My 330/88 and M. kansasii 6 509/96, respectively, by applying the micromethod for the determination of the minimum inhibitory concentration (MIC). It is concludut that the molucules posscssed selatively promising activity against M. Tuberculasis and M. Kansas!!.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FR - Pharmacology and apothecary chemistry
OECD FORD branch
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Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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