The in Vitro Evaluation of ortho-/meta-/para-Alkoxyphenylcarbamic Acid Esters Containing Substituted N-Phenylpiperazin-1-yl Fragment against Mycobacterium tuberculosis H37Ra Strain.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F14%3A43873237" target="_blank" >RIV/62157124:16370/14:43873237 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The in Vitro Evaluation of ortho-/meta-/para-Alkoxyphenylcarbamic Acid Esters Containing Substituted N-Phenylpiperazin-1-yl Fragment against Mycobacterium tuberculosis H37Ra Strain.
Popis výsledku v původním jazyce
The purpose of current paper was to in vitro screen the set of ortho-/meta-/para-alkoxyphenylcarbamic acid esters containing 4-(3--trifluoromethylphenyl)piperazin-1-yl moiety for their potency against avirulent Mycobacterium (M.) tuberculosis H37Ra by applying the micromethod for the determination of the minimum inhibitory concentration (MIC). Considered mycobacterial strain was grown in Middlebrook broth, supplemented with Oleic-Albumin-Dextrose-Catalase supplement and mycobactin J (2 mýg/mL) as well.The susceptibility of the strain was investigated in a 96-well plate format, the plates were incubated at 37°C for 7 days. According to estimated MIC readouts it was concluded that para-alkoxy substitution within lipophilic fragment would be favorable for the activity of currently investigated compounds against given mycobacterium. On the other hand, relatively high lipophilicity was not regarded as crucial factor which determined the activity profile of inspected derivatives. Moreover,
Název v anglickém jazyce
The in Vitro Evaluation of ortho-/meta-/para-Alkoxyphenylcarbamic Acid Esters Containing Substituted N-Phenylpiperazin-1-yl Fragment against Mycobacterium tuberculosis H37Ra Strain.
Popis výsledku anglicky
The purpose of current paper was to in vitro screen the set of ortho-/meta-/para-alkoxyphenylcarbamic acid esters containing 4-(3--trifluoromethylphenyl)piperazin-1-yl moiety for their potency against avirulent Mycobacterium (M.) tuberculosis H37Ra by applying the micromethod for the determination of the minimum inhibitory concentration (MIC). Considered mycobacterial strain was grown in Middlebrook broth, supplemented with Oleic-Albumin-Dextrose-Catalase supplement and mycobactin J (2 mýg/mL) as well.The susceptibility of the strain was investigated in a 96-well plate format, the plates were incubated at 37°C for 7 days. According to estimated MIC readouts it was concluded that para-alkoxy substitution within lipophilic fragment would be favorable for the activity of currently investigated compounds against given mycobacterium. On the other hand, relatively high lipophilicity was not regarded as crucial factor which determined the activity profile of inspected derivatives. Moreover,
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FR - Farmakologie a lékárnická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2014
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Microbiology, Biotechnology and Food Sciences
ISSN
1338-5178
e-ISSN
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Svazek periodika
3
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
SK - Slovenská republika
Počet stran výsledku
3
Strana od-do
395-397
Kód UT WoS článku
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EID výsledku v databázi Scopus
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