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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>17</Volume><Issue>4</Issue><PubDate PubStatus="epublish"><Year>2015</Year><Month>12</Month><Day>13</Day></PubDate></Journal><ArticleTitle>Correlation between lipophilicity and antimicrobial activity of some 2-(4-substituted phenyl)-3(2H)-isothiazolones</ArticleTitle><FirstPage>256</FirstPage><LastPage>263</LastPage><AuthorList><Author><FirstName>S</FirstName><LastName>Rezaee</LastName></Author><Author><FirstName>A</FirstName><LastName>Khalaj</LastName></Author><Author><FirstName>N</FirstName><LastName>Adibpour</LastName></Author><Author><FirstName>M</FirstName><LastName>Saffary</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>12</Month><Day>13</Day></PubDate></History><Abstract>&amp;nbsp;

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Background and purpose of the study

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. 3(2H)-Isothiazolones have shown antimicrobial activity and have been used as preservative in different products. However, reports on their structure-antimicrobial activity relationship are scanty. The aim of this study was to determine the relationship between lipophilicity and antimicrobial activity of several 2- (4-substituted phenyl) -3(2H)-isothiazolones of which some have shown antibacterial activities similar or higher than gentamycin, ceftazidime, ceftriaxone, ciprofloxacin , and antifungal activites similar or higher than itraconazole and ketoconazole as reference drugs.Methods. Partition coefficient (log Po/w) of the tested compounds was determined experimentally by a reversed- phase high performance liquid chromatography method using octadecyl-poly(vinyl alcohol) (ODP) column and methanol-water gradient as mobile phase and theoretically by Clog P and ALOGPS computer programs. Results. The HPLC and theoretical log Po/wvalues showed potential correlations which indicate that both experimental and theoretical methods are equally suitable to predict lipophilicity of 3(2H)-isothiazolones. There were also significant correlations between MICs (minimum inhibitory concentrations) of 5-chloro substituted 3(2H)- isothiazolnes against Salmonella typhimurium and Escherichia coli and experimentally determined log Po/wvalues, as well as MICs of 5-unsubstituted 3(2H)- isothiazolnes against E. coli and ALOGPS values. The antifungal activity of the tested compounds against Tricophyton. mentagrophytes and M.canis increased with increase in the experimental and theoretical log P values , but this increase was only significant for the activity against 

Microsporum. canis.




&amp;nbsp;</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/553</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/553/442</pdf_url></Article></Articles>
