Literature DB >> 16168643

Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents.

Sanjay Babu Katiyar1, Kumkum Srivastava, S K Puri, Prem M S Chauhan.   

Abstract

A series of 22 compounds were synthesized and screened against Plasmodium falciparum NF-54 strain. Of the screened compounds, 6 compounds showed MIC in the range between 1 and 2 microg/mL. These compounds are 32 times more potent than the cycloguanil which was used as the standard drug.

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Year:  2005        PMID: 16168643     DOI: 10.1016/j.bmcl.2005.08.023

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  N4-phenyl modifications of N2-(2-hydroxyl)ethyl-6-(pyrrolidin-1-yl)-1,3,5-triazine-2,4-diamines enhance glucocerebrosidase inhibition by small molecules with potential as chemical chaperones for Gaucher disease.

Authors:  Wenwei Huang; Wei Zheng; Daniel J Urban; James Inglese; Ellen Sidransky; Christopher P Austin; Craig J Thomas
Journal:  Bioorg Med Chem Lett       Date:  2007-08-28       Impact factor: 2.823

2.  Catalyst-free, one-pot, three-component synthesis of 5-amino-1,3-aryl-₁Η-pyrazole-4-carbonitriles in green media.

Authors:  Alireza Hasaninejad; Somayeh Firoozi
Journal:  Mol Divers       Date:  2013-04-27       Impact factor: 2.943

3.  Importance of secondary screening with clinical isolates for anti-leishmania drug discovery.

Authors:  Aya Hefnawy; Juan Cantizani; Imanol Peña; Pilar Manzano; Suman Rijal; Jean-Claude Dujardin; Geraldine De Muylder; Julio Martin
Journal:  Sci Rep       Date:  2018-08-06       Impact factor: 4.379

  3 in total

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