| Literature DB >> 23919553 |
Abstract
Recent initiatives to develop more effective and affordable drugs, controlling mosquitoes and development of a preventative vaccine have been launched with the goal of completely eradicating <span class="Disease">malaria. To this end, Novartis (Surrey, UK) and GlaxoSmithKline (Middlesex, UK) screened their chemical libraries of approximately two million small molecules for anti<span class="Disease">malarial properties, which resulted in a set of over 20,000 'highly druggable' initial hits. Efforts in academia are centered on specific pathway targets. One such high-throughput screening effort has been focused on hemozoin formation, a unique heme detoxification pathway found in the malaria parasite. This review discusses the current approaches and limitations of high-throughput screening discovery of hemozoin inhibitors. In the future, new methods must be developed to validate the mechanism of action of these hit compounds within the parasite.Entities:
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Year: 2013 PMID: 23919553 PMCID: PMC4928194 DOI: 10.4155/fmc.13.113
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808