| Literature DB >> 30104093 |
Michael G Thomas1, Manu De Rycker1, Ignacio Cotillo Torrejon2, John Thomas1, Jennifer Riley1, Daniel Spinks1, Kevin D Read1, Tim J Miles2, Ian H Gilbert1, Paul G Wyatt3.
Abstract
Chagas' disease, caused by the protozoan parasite Trypanosoma cruzi, affects 8-10 million people across the Latin American population and is responsible for around 12,500 deaths per annum. The current frontline treatments, benznidazole and nifurtimox, are associated with side effects and lack efficacy in the chronic stage of the disease, leading to an urgent need for new treatments. A high throughput screening campaign against the physiologically relevant intracellular form of the parasite identified a series of 2,4-diamino-6-methylpyrimidines. Demonstrating the series did not work through the anti-target TcCYP51, and was generally cytocidal, confirmed its suitability for further development. This study reports the optimisation of selectivity and metabolic stability of the series and identification of a suitable lead for further optimisation.Entities:
Keywords: Chagas’ disease; SAR studies; Trypanosoma cruzi
Mesh:
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Year: 2018 PMID: 30104093 PMCID: PMC6970618 DOI: 10.1016/j.bmcl.2018.08.005
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.940