Chemical Structure : DMU759
Catalog No.: PC-24979Not For Human Use, Lab Use Only.
DMU759 is a specific inhibitor of T. cruzi lysyl-tRNA synthetase 1 (TcKRS1) with IC50 of 15 nM, demonstrates potent activity against T. cruzi (Sylvio X10/7A1strain) with EC50 of 14 nM.
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DMU759 is a specific inhibitor of T. cruzi lysyl-tRNA synthetase 1 (TcKRS1) with IC50 of 15 nM, demonstrates potent activity against T. cruzi (Sylvio X10/7A1strain) with EC50 of 14 nM.
DMU759 is pan-active against all kinetoplastid parasites.
DMU759 binds to the ATP-binding pocket of KRS1.
DMU759 is not a potent inhibitor of the human ortholog of KRS1 with IC50 of >7000 nM.
DMU759 (50 mg/kg, twice a day) is capable of reducing parasitemia by up to 81% in mouse model of acute T. cruzi infection.
M.Wt | 327.37 | |
Formula | C15H16F3N3S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Tulloch LB, et al. Sci Transl Med. 2025 Jul 9;17(806):eadu4564.
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