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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/43406
Title: Thienopyrimidine sulphonamide hybrids: Design, synthesis, antiprotozoal activity and molecular docking studies
Authors: Saadia Leeza Zaidi
Subhash M. Agarwal
Porntip Chavalitshewinkoon-Petmitr
Thidarat Suksangpleng
Kamal Ahmad
Fernando Avecilla
Amir Azam
Jamia Millia Islamia
Institute of Cytology and Preventive Oncology Noida
Mahidol University
Centre for Interdisciplinary Research in Basic Science
Universidade da Coruña
Keywords: Chemical Engineering;Chemistry
Issue Date: 1-Jan-2016
Citation: RSC Advances. Vol.6, No.93 (2016), 90371-90383
Abstract: © 2016 The Royal Society of Chemistry. A series of hybrid compounds containing the thienopyrimidine scaffold as a DHFR inhibitor fused with a bioactive sulphonamide piperazine skeleton were synthesized and evaluated against the chloroquine and pyrimethamine resistant K1 strain of Plasmodium falciparum and the HM1:1MSS strain of Entamoeba histolytica, respectively. A few of the compounds showed better results than the standard drugs. The toxicity of the hybrids was measured on the Chinese hamster cell line. The majority of the compounds had low toxicity. The binding modes of the most potent antimalarial compounds (5, 6 and 8) were also investigated against PfDHFR using molecular docking and enzyme binding studies, whereby 5 and 6 were found to the most promising against PfDHFR. The present studies suggest that these hybrids might be possible antiprotozoal lead compounds worth further investigation.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84989222451&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/43406
ISSN: 20462069
Appears in Collections:Scopus 2016-2017

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