Atovaquone (Atavaquone) is a potent, selective and orally active inhibitor of the parasites mitochondrial cytochrome bc1 complex. Atovaquone is against human and P. falciparum cytochrome bc1 activity with IC50 values of 460 nM and 2.0 nM, respectively. Atovaquone is an antimalarial agent and has the potential for the investigation of neumocystis pneumonia, toxoplasmosis, malaria, and babesia[1][2].
Molecular Weight:
366.84
Purity:
99.75
CAS Number:
[95233-18-4]
Formula:
C22H19ClO3
Target:
Antibiotic,Bacterial,Cytochrome P450,Parasite
Application Notes:
MCE Product type: Reference compound
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