PF-06250112

Modify Date: 2025-09-21 13:07:33

PF-06250112 Structure
PF-06250112 structure
Common Name PF-06250112
CAS Number 1609465-89-5 Molecular Weight 438.43
Density N/A Boiling Point N/A
Molecular Formula C22H20F2N6O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of PF-06250112


PF-06250112 is a potent, highly selective, orally bioavailable BTK inhibitor with an IC50 of 0.5 nM, shows inhibitory effect toward BMX nonreceptor tyrosine kinase and TEC with IC50s of 0.9 nM and 1.2 nM, respectively[1].

 Names

Name PF-06250112

 PF-06250112 Biological Activity

Description PF-06250112 is a potent, highly selective, orally bioavailable BTK inhibitor with an IC50 of 0.5 nM, shows inhibitory effect toward BMX nonreceptor tyrosine kinase and TEC with IC50s of 0.9 nM and 1.2 nM, respectively[1].
Related Catalog
Target

IC50: 0.5 nM (BTK), 0.9 nM (BMX), 1.2 nM (TEC)[1]

References

[1]. Rankin AL, et al. Selective inhibition of BTK prevents murine lupus and antibody-mediated glomerulonephritis. J Immunol. 2013 Nov 1;191(9):4540-50.

 Chemical & Physical Properties

Molecular Formula C22H20F2N6O2
Molecular Weight 438.43
InChIKey SQFDBQCBXUWICP-HNNXBMFYSA-N
SMILES N#CN1CCCC(n2nc(-c3ccc(Oc4ccc(F)cc4F)cc3)c(C(N)=O)c2N)C1
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