Literature DB >> 10719621

Inhibition of cryptosporidium parvum in vitro by 9-(alkylthio)acridine derivatives.

L Khalifa1, M J Rosales, C Mascaro, J Karolak-Wojciechowska, N Bsiri, P Brouant, J Barbe.   

Abstract

The synthesis of several acridinic thioethers is described. Compounds prepared were tested in vitro as potential drugs against the opportunistic infection known as cryptosporidiosis. With a view to predict activity, the quantitative structure-activity relationships were investigated. Correlations between experimental data and either log P or pKa are discussed.

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Year:  2000        PMID: 10719621     DOI: 10.1055/s-0031-1300183

Source DB:  PubMed          Journal:  Arzneimittelforschung        ISSN: 0004-4172


  1 in total

1.  Dicyclic and tricyclic diaminopyrimidine derivatives as potent inhibitors of Cryptosporidium parvum dihydrofolate reductase: structure-activity and structure-selectivity correlations.

Authors:  R G Nelson; A Rosowsky
Journal:  Antimicrob Agents Chemother       Date:  2001-12       Impact factor: 5.191

  1 in total

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