Chemical Structure : FLC-8
Catalog No.: PC-26471Not For Human Use, Lab Use Only.
FLC-8 is a potent, selective and covalent FLT3 inhibitor with IC50 of 10.2 nM, 11.6 nM and 24.1 nM for FLT3-WT, FLT3 G697R and FLT3 N676D respectively.
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FLC-8 is a potent, selective and covalent FLT3 inhibitor with IC50 of 10.2 nM, 11.6 nM and 24.1 nM for FLT3-WT, FLT3 G697R and FLT3 N676D respectively.
FLC-8 covalently target Cys807, a nucleophilic residue within the FLT3 kinase domain.
FLC-8 suppressed FLT3-mediated STAT5, AKT, and ERK signaling and induced apoptosis in AML cells while maintaining low-nanomolar potency over 72 h.
FLC-8 inhibited MV4-11 xenograft growth (TGI: 136–178% at 10–50 mg/kg) without overt toxicity.
| M.Wt | 496.45 | |
| Formula | C24H19F3N6O3 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Wang ZX, et al. J Med Chem. 2026 Apr 3. doi: 10.1021/acs.jmedchem.6c00511.

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