
CHMFL-BMX-078
CAS No. 1808288-51-8
CHMFL-BMX-078( CHMFL-BMX-078 | CHMFL-BMX 078 | CHMFL BMX 078 | CHMFLBMX078 )
Catalog No. M12769 CAS No. 1808288-51-8
CHMFL-BMX-078 is a highly selective, potent, type II irreversible BMX kinase inhibitor with IC50 of 11 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 177 | In Stock |
![]() ![]() |
10MG | 282 | In Stock |
![]() ![]() |
25MG | 531 | In Stock |
![]() ![]() |
50MG | 767 | In Stock |
![]() ![]() |
100MG | 1053 | In Stock |
![]() ![]() |
200MG | Get Quote | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameCHMFL-BMX-078
-
NoteResearch use only, not for human use.
-
Brief DescriptionCHMFL-BMX-078 is a highly selective, potent, type II irreversible BMX kinase inhibitor with IC50 of 11 nM.
-
DescriptionCHMFL-BMX-078 is a highly selective, potent, type II irreversible BMX kinase inhibitor with IC50 of 11 nM; displays a high selectivity profile (S score(1) = 0.01) against the 468 kinases/mutants in the KINOMEscan evaluation and achieved at least 40-fold selectivity over BTK kinase; CHMFL-BMX-078 is a useful pharmacological tool to elucidate the detailed mechanism of BMX mediated signaling pathways.
-
In VitroBone marrow kinase in the X chromosome (BMX, also called ETK) is a nonreceptor tyrosine kinase involved in tumorigenicity, cell motility, adhesion, angiogenesis, proliferation, and differentiation. CHMFL-BMX-078 exhibits an IC50 of 11 nM by formation of a covalent bond with cysteine 496 residue in the DFG-out inactive conformation of BMX. It displays a high selectivity profile against the 468 kinases/mutants in the KINOMEscan evaluation and achieves at least 40-fold selectivity over BTK kinase (IC50=437 nM). For inactive state of BMX kinase, CHMFL-BMX-078 displays a binding Kd of 81 nM, while for the active state of BMX kinase, it exhibits a binding Kd of 10200 nM. CHMFL-BMX-078 exhibits antiproliferative effects against BaF3-TEL-BMX cells (GI50=0.016 μM) and selectivity over parental BaF3 cells. CHMFL-BMX-078 is about 80-fold more potent against BMX wt (EC50=5.8 nM) than C496S mutant (EC50=459 nM) for the inhibition of BMX total tyrosine phosphorylation. CHMFL-BMX-078 would serve as a useful pharmacological tool to elucidate the detailed mechanism of BMX mediated signaling pathways.
-
In VivoCHMFL-BMX-078 exhibits a short half-life (T1/2=0.80 h) in iv injection. CHMFL-BMX-078 also displays an acceptable Cmax (13565.23 ng/mL) and AUC0-t (1386.41 ng/mL h) in iv injection. However, it is not absorbed by oral administration, indicating that this compound could be administrated through iv or ip injection when used as a research tool.
-
SynonymsCHMFL-BMX-078 | CHMFL-BMX 078 | CHMFL BMX 078 | CHMFLBMX078
-
PathwayTyrosine Kinase
-
TargetBMX Kinase
-
RecptorBmx
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1808288-51-8
-
Formula Weight625.686
-
Molecular FormulaC33H35N7O6
-
Purity>98% (HPLC)
-
SolubilityDMSO: Soluble ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESO=C(C1=CN=C(NC2=CC=C(C)C(NC(C=C)=O)=C2)N=C1NC)NC3=CC(NC(C4=CC(OC)=C(OC)C(OC)=C4)=O)=CC=C3C
-
Chemical Name2-((3-Acrylamido-4-methylphenyl)amino)-N-(2-methyl-5-(3,4,5-trimethoxybenzamido)phenyl)-4-(methylamino)pyrimidine-5-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Liang X, et al. J Med Chem. 2017 Mar 9;60(5):1793-1816.
molnova catalog



related products
-
CTN06
CTN06 is a potent Etk (BMX) and Btk dual inhibitor with IC50 of 200 and 50 nM, respectively.
-
CTA095
CTA095 (CTA-095) is a potent Etk (BMX) and Src dual inhibitor with IC50 of 60 and 120 nM, respectively.
-
CHMFL-BMX-078
CHMFL-BMX-078 is a highly selective, potent, type II irreversible BMX kinase inhibitor with IC50 of 11 nM.