Khadija Abdelrahmman , Mohammed F. El-Behairy , Muhammad A. Alsherbiny , Tarek E. Mazeed
{"title":"二氢吡唑衍生物对念珠菌的体外活性研究","authors":"Khadija Abdelrahmman , Mohammed F. El-Behairy , Muhammad A. Alsherbiny , Tarek E. Mazeed","doi":"10.1016/j.bfopcu.2017.11.002","DOIUrl":null,"url":null,"abstract":"<div><p>Profound insights for efficient antifungal agents are required for the increased hazardous fungal infections caused by yeast, such as <em>Candida</em> species. In this study, we investigate the efficacy of different benzodioxolpyrazoline derivatives against two <em>Candida</em> species. All compounds exhibited potent <em>in vitro</em> antifungal activity against both species. Compound <strong>5</strong> showed the best inhibition zone in comparison to positive controls for <em>Candida albicans</em>. For <em>Candida parapsilosis</em>, all the tested compounds were active while the positive controls were inactive. These compounds provide good starting models for the development of new antimicrobial agents which could be useful especially for the treatment of candidiasis.</p></div>","PeriodicalId":9369,"journal":{"name":"Bulletin of Faculty of Pharmacy, Cairo University","volume":"56 1","pages":"Pages 80-82"},"PeriodicalIF":0.0000,"publicationDate":"2018-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bfopcu.2017.11.002","citationCount":"6","resultStr":"{\"title\":\"In vitro activity of dihydropyrazole derivatives against Candida species\",\"authors\":\"Khadija Abdelrahmman , Mohammed F. El-Behairy , Muhammad A. Alsherbiny , Tarek E. Mazeed\",\"doi\":\"10.1016/j.bfopcu.2017.11.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Profound insights for efficient antifungal agents are required for the increased hazardous fungal infections caused by yeast, such as <em>Candida</em> species. In this study, we investigate the efficacy of different benzodioxolpyrazoline derivatives against two <em>Candida</em> species. All compounds exhibited potent <em>in vitro</em> antifungal activity against both species. Compound <strong>5</strong> showed the best inhibition zone in comparison to positive controls for <em>Candida albicans</em>. For <em>Candida parapsilosis</em>, all the tested compounds were active while the positive controls were inactive. These compounds provide good starting models for the development of new antimicrobial agents which could be useful especially for the treatment of candidiasis.</p></div>\",\"PeriodicalId\":9369,\"journal\":{\"name\":\"Bulletin of Faculty of Pharmacy, Cairo University\",\"volume\":\"56 1\",\"pages\":\"Pages 80-82\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.bfopcu.2017.11.002\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of Faculty of Pharmacy, Cairo University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1110093117300625\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Faculty of Pharmacy, Cairo University","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1110093117300625","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In vitro activity of dihydropyrazole derivatives against Candida species
Profound insights for efficient antifungal agents are required for the increased hazardous fungal infections caused by yeast, such as Candida species. In this study, we investigate the efficacy of different benzodioxolpyrazoline derivatives against two Candida species. All compounds exhibited potent in vitro antifungal activity against both species. Compound 5 showed the best inhibition zone in comparison to positive controls for Candida albicans. For Candida parapsilosis, all the tested compounds were active while the positive controls were inactive. These compounds provide good starting models for the development of new antimicrobial agents which could be useful especially for the treatment of candidiasis.