To investigate the antileishmanial activity of novel azole compounds against , which causes deadly visceral leishmaniasis disease. A focused azole-based library was screened against both promastigotes and amastigotes forms of strains in flat-bottomed 96-well tissue culture plates and J774A.1 macrophage cell-line infected with . The comprehensive screening of azole-based library against strains provided novel hits, which can serve as a good starting point to initiate hit to lead optimization campaign. Hits identified from azole-based library exhibited potent activity against promastigotes and amastigotes of . These potent novel azole hits could be a good starting point to carry out for further medicinal chemistry exploration for antileishmania program.
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http://dx.doi.org/10.2217/fmb-2020-0320 | DOI Listing |
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