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Biochem/physiol Actions
Cell penetrant, selective and potent multi-targeting bioenergetic inhibitor of succinate dehydrogenase and the F1Fo-ATP synthase in Mycobacterium tuberculosis; bactericidal antibiotic in MTB.
BB2-50F, an amiloride derivative, is a cell penetrant, selective and potent multi-targeting bioenergetic inhibitor of succinate dehydrogenase and the F1Fo-ATP synthase in Mycobacterium tuberculosis. BB2-50F act as fast acting bactericidal antibiotic in both replicating and nonreplicating cultures of M. tuberculosis (MIC = 2.6 µM in M. tuberculosis mc2 6230). BB2-50F is a potent inhibitor of bacterial motility.
| Quality Level | 100 |
| assay | ≥98% (HPLC) |
| form | powder |
| color | white to beige |
| solubility | DMSO: 2 mg/mL, clear |
| storage temp. | 2-8°C |
| SMILES string | NC(NC(C1=NC(C2=CC(C=CC=C3)=C3O2)=C(N4CCCCCC4)N=C1N)=O)=N |
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