Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/223196
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Title

Medicinal Chemistry Optimization of a Diaminopurine Chemotype: Toward a Lead for Trypanosoma brucei Inhibitors

AuthorsSingh, Baljinder; Díaz-González, Rosario; Ceballos-Pérez, Gloria; Rojas-Barros, Domingo I.; Gunaganti, Naresh; Gillingwater, Kirsten; Santos Martinez-Martinez, María; Manzano, Pilar; Navarro, M.; Pollastri, M.P.
Issue Date2020
PublisherAmerican Chemical Society
CitationJournal of Medicinal Chemistry 63: 9912- 9927 (2020)
AbstractHuman African trypanosomiasis (HAT), or sleeping sickness, is caused by the protozoan parasite Trypanosoma brucei and transmitted through the bite of infected tsetse flies. The disease is considered fatal if left untreated. To identify new chemotypes against Trypanosoma brucei, previously we identified 797 potent kinase-targeting inhibitors grouped into 59 clusters plus 53 singleton compounds with at least 100-fold selectivity over HepG2 cells. From this set of hits, a cluster of diaminopurine-derived compounds was identified. Herein, we report our medicinal chemistry investigation involving the exploration of structure¿activity and structure¿property relationships around one of the high-throughput screening (HTS) hits, N2-(thiophen-3-yl)-N6-(2,2,2-trifluoroethyl)-9H-purine-2,6-diamine (1, NEU-1106). This work led to the identification of a potent lead compound (4aa, NEU-4854) with improved in vitro absorption, distribution, metabolism, and excretion (ADME) properties, which was progressed into proof-of-concept translation of in vitro antiparasitic activity to in vivo efficacy.
Publisher version (URL)http://dx.doi.org/10.1021/acs.jmedchem.0c01017
URIhttp://hdl.handle.net/10261/223196
DOI10.1021/acs.jmedchem.0c01017
Identifiersdoi: 10.1021/acs.jmedchem.0c01017
issn: 0022-2623
e-issn: 1520-4804
Appears in Collections:(IPBLN) Artículos

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