η-Class Carbonic Anhydrases as Antiplasmodial Drug Targets: Current State of the Art and Hurdles to Develop New Antimalarials

Author:

Capasso Clemente,Supuran Claudiu T.

Publisher

Springer International Publishing

Reference102 articles.

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2. Syrjanen L, Vermelho AB, Rodrigues Ide A, Corte-Real S, Salonen T, Pan P et al (2013) Cloning, characterization, and inhibition studies of a beta-carbonic anhydrase from Leishmania donovani chagasi, the protozoan parasite responsible for leishmaniasis. J Med Chem 56(18):7372–7381. https://doi.org/10.1021/jm400939k

3. Alafeefy AM, Ceruso M, Al-Jaber NA, Parkkila S, Vermelho AB, Supuran CT (2015) A new class of quinazoline-sulfonamides acting as efficient inhibitors against the alpha-carbonic anhydrase from Trypanosoma cruzi. J Enzyme Inhib Med Chem 30(4):581–585. https://doi.org/10.3109/14756366.2014.956309

4. de Menezes DD, Calvet CM, Rodrigues GC, de Souza Pereira MC, Almeida IR, de Aguiar AP et al (2015) Hydroxamic acid derivatives: a promising scaffold for rational compound optimization in Chagas disease. J Enzyme Inhib Med Chem:1–10. https://doi.org/10.3109/14756366.2015.1077330

5. Guzel-Akdemir O, Akdemir A, Pan P, Vermelho AB, Parkkila S, Scozzafava A et al (2013) A class of sulfonamides with strong inhibitory action against the alpha-carbonic anhydrase from Trypanosoma cruzi. J Med Chem 56(14):5773–5781. https://doi.org/10.1021/jm400418p

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