BASIC ESTERS OF meta-/para-ALKOXYPHENYLCARBAMIC ACID CONTAINING 4-(2-METHYL-/2-FLUOROPHENYL)PIPERAZIN-1-YL MOIETY AND THEIR ANTIMICROBIAL ACTIVITY

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F13%3A43872345" target="_blank" >RIV/62157124:16370/13:43872345 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

BASIC ESTERS OF meta-/para-ALKOXYPHENYLCARBAMIC ACID CONTAINING 4-(2-METHYL-/2-FLUOROPHENYL)PIPERAZIN-1-YL MOIETY AND THEIR ANTIMICROBIAL ACTIVITY

Popis výsledku v původním jazyce

The original esters of meta-/para-alkoxyphenylcarbamic acid containing 4-(2-methyl-/2-fluorophenyl)piperazin-1-yl, labelled as 5d-7d, were screened for their in vitro antimicrobial activity against Staphylococcus aureus, Escherichia coli and Candida albicans, respectively. Following the minimum inhibitory concentration (MIC) assay, electronic and hydrophobic interactions, induced by suitable substitution at the N-phenylpiperazine, ring have appeared to be more noticabe factors which positively influenced the efficiency of these compounds against S. aureus as well as against E. coli than relatively high lipophilicity of 5d-7d. In general, the compounds comprising methyl substituent attached to basic fragment (7a-7d) were observed to be more active against both given bacterial strains in the comparison to those with fluoro group (5d and 5e). From the entire analyzed set, the most active molecule 7b showed MIC=0.10 mg.mL(-1) against given Gram-positive and Gram-negative bacteria as well.

Název v anglickém jazyce

BASIC ESTERS OF meta-/para-ALKOXYPHENYLCARBAMIC ACID CONTAINING 4-(2-METHYL-/2-FLUOROPHENYL)PIPERAZIN-1-YL MOIETY AND THEIR ANTIMICROBIAL ACTIVITY

Popis výsledku anglicky

The original esters of meta-/para-alkoxyphenylcarbamic acid containing 4-(2-methyl-/2-fluorophenyl)piperazin-1-yl, labelled as 5d-7d, were screened for their in vitro antimicrobial activity against Staphylococcus aureus, Escherichia coli and Candida albicans, respectively. Following the minimum inhibitory concentration (MIC) assay, electronic and hydrophobic interactions, induced by suitable substitution at the N-phenylpiperazine, ring have appeared to be more noticabe factors which positively influenced the efficiency of these compounds against S. aureus as well as against E. coli than relatively high lipophilicity of 5d-7d. In general, the compounds comprising methyl substituent attached to basic fragment (7a-7d) were observed to be more active against both given bacterial strains in the comparison to those with fluoro group (5d and 5e). From the entire analyzed set, the most active molecule 7b showed MIC=0.10 mg.mL(-1) against given Gram-positive and Gram-negative bacteria as well.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FR - Farmakologie a lékárnická chemie

OECD FORD obor

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Projekt

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Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2013

Kód důvěrnosti údajů

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

Název periodika

Fresenius Environmental Bulletin

ISSN

1018-4619

e-ISSN

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Svazek periodika

22

Číslo periodika v rámci svazku

9A

Stát vydavatele periodika

DE - Spolková republika Německo

Počet stran výsledku

6

Strana od-do

2689-2694

Kód UT WoS článku

000326911800008

EID výsledku v databázi Scopus

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