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We report that the tuberculosis drug SQ109 (N-adamantan-2-yl-N'-((E)-3,7-dimethyl-octa-2,6-dienyl)-ethane-1,2-diamine) has potent activity against the intracellular, amastigote form of Leishmania mexicana (IC50 ~11 nM) with a good selectivity index (>500). It is also active against promastigotes (IC50 ~ 500 nM) and acts as a protonophore uncoupler, in addition to disrupting Ca2+ homeostasis by releasing organelle Ca2+ into the cytoplasm and as such it is an interesting new leishmaniasis drug hit candidate.
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This page is a summary of: Inhibition of Leishmania mexicana Growth by the Tuberculosis Drug SQ109, Antimicrobial Agents and Chemotherapy, July 2016, ASM Journals,
DOI: 10.1128/aac.00945-16.
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