Chemical Structure : ML901
货号: PC-23600Not For Human Use, Lab Use Only.
ML901 is a potent, specific inhibitor of P. falciparum tyrosine tRNA synthetase (PfYRS, PfTyrRS), shows potent activity against P. falciparum with IC50 of 2.0 nM.
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ML901 is a potent, specific inhibitor of P. falciparum tyrosine tRNA synthetase (PfYRS, PfTyrRS), shows potent activity against P. falciparum with IC50 of 2.0 nM.
ML901 targets PfYRS and inhibits protein translation, by a reaction-hijacking mechanism.
ML901 retained activity against all strains of P. falciparum tested, regardless of their resistance profile and geographical origin.
ML901 triggers eIF2α phosphorylation in wildtype P. falciparum (Cam3.II_rev).
ML901 exerts activity against human Atg7 (IC50 = 33 nM), but has much weaker activity against other E1 enzymes.
ML901 single dose (50 mg/kg i.p.) exhibits in vivo antimalarial efficacy oin severe combined immune deficient (SCID) mice, engrafted with P. falciparum infected human RBCs.
分子量 | 412.32 | |
分子式 | C11H14F2N6O7S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Xie SC, et al. Science. 2022 Jun 3;376(6597):1074-1079.
2. Xie SC, et al. PLoS Pathog. 2024 Dec 9;20(12):e1012429.
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