Literature DB >> 32668631

4-Arylthieno[2,3-b]pyridine-2-carboxamides Are a New Class of Antiplasmodial Agents.

Sandra I Schweda1,2, Arne Alder3,4,5, Tim Gilberger3,4,5, Conrad Kunick1,2.   

Abstract

Malaria causes hundreds of thousands of deaths every year, making it one of the most dangerous infectious diseases worldwide. Because the pathogens have developed resistance against most of the established anti-malarial drugs, new antiplasmodial agents are urgently needed. In analogy to similar antiplasmodial ketones, 4-arylthieno[2,3-b]pyridine-2-carboxamides were synthesized by Thorpe-Ziegler reactions. In contrast to the related ketones, these carboxamides are only weak inhibitors of the plasmodial enzyme PfGSK-3 but the compounds nevertheless show strong antiparasitic activity. The most potent representatives inhibit the pathogens with IC50 values in the two-digit nanomolar range and exhibit high selectivity indices (>100).

Entities:  

Keywords:  PfGSK-3; Plasmodium falciparum; Thorpe-Ziegler reaction; anti-malarial drugs; antiplasmodial; malaria; thieno[2,3-b]pyridine

Mesh:

Substances:

Year:  2020        PMID: 32668631      PMCID: PMC7397174          DOI: 10.3390/molecules25143187

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  22 in total

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Journal:  J Org Chem       Date:  2003-10-03       Impact factor: 4.354

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Review 7.  Plasmodium falciparum glycogen synthase kinase-3: molecular model, expression, intracellular localisation and selective inhibitors.

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9.  Malaria: Global progress 2000 - 2015 and future challenges.

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10.  The prevalence of Plasmodium falciparum in sub-Saharan Africa since 1900.

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