FGFRs-IN-1
FGFRs-IN-1 (Compound A16) is the orally active inhibitor for FGFR, that inhibits FGFR1/2/3/4 with IC50s of 2.3, 7, 11, and 163 nM, respectively. FGFRs-IN-1 also inhibits VEGFR1/2/3, Abl, and Flt3 with IC50s of 61, 176, 112, 26, and 353 nM, respectively. FGFRs-IN-1 exhibits weak inhibitory efficacy against CYP enzymes. FGFRs-IN-1 reduces the expression of α-SMA and collagen I, and inhibits epithelial-mesenchymal transition (EMT) in TGF-β1 stimulated A549 cell. FGFRs-IN-1 exhibits anti-inflammatory activity in Bleomycin (HY-17565)-induced mouse pulmonary fibrosis model and CCl4 (HY-Y0298)-induced mouse liver fibrosis model.
Para uso exclusivo en investigación. No vendemos a pacientes.
- Fòrmula: C28H26Cl2N4O3
- Peso molecular:537.44
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Actividad biológica
-
Chemical Information
- Pureza y Documentación
- Referencias
-
Help & FAQs
Ver todos los productos específicos de isoformas VEGFR
More
Actividad biológica
|
FGFR1 2.3 nM (IC50) |
FGFR2 7 nM (IC50) |
FGFR3 11 nM (IC50) |
Abl 26 nM (IC50) |
Flt-1 61 nM (IC50) |
Flt-4 112 nM (IC50) |
FGFR4 163 nM (IC50) |
KDR 176 nM (IC50) |
Flt3 353 nM (IC50) |
CYP2D6 9.27 μM (IC50) |
CYP2C19 11.46 μM (IC50) |
CYP1A2 26.33 μM (IC50) |
Chemical Information
-
Peso molecular 537.44
-
Fòrmula C28H26Cl2N4O3
-
SMILES
O=C(C1=CC=C(/C=C/C2=NNC3=C2C=CC(C4=C(Cl)C(OC)=CC(OC)=C4Cl)=C3)C=C1)N5CCNCC5
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
Referencias
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
FGFRs-IN-1 Related Classifications
HY-170846 Related Classifications
Powered by Bioz