PP487
PP487 is a selective dual inhibitor of Tyrosine kinase/PI3-K, with IC50 values of 0.017 μM, 0.072 μM, 0.004 μM, 0.01 μM, 0.55 μM, 0.22 μM, and < 0.01 μM against DNA-PK, mTOR, Hck, Src, EGFR, EphB4, and PDGFR, respectively. PP487 can be used in cancer research.
Para uso exclusivo en investigación. No vendemos a pacientes.
- No. CAS: 1092787-12-6
- Fòrmula: C14H14BrN5O
- Peso molecular:348.20
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
Ver todos los productos específicos de isoformas VEGFR
MoreVer todos los productos específicos de isoformas EGFR
More
Actividad biológica
|
p110α 0.046 μM (IC50) |
p110β 0.24 μM (IC50) |
p110δ 0.027 μM (IC50) |
p110γ 0.1 μM (IC50) |
Abl 0.021 μM (IC50) |
VEGFR2 0.055 μM (IC50) |
PP487 (0.001-50 µM) potently inhibits nanomolar-concentration tyrosine kinases (including Src) as well as members of the PI3-K family (including mTOR), while maintaining high selectivity toward the serine-threonine kinase panel[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
No. CAS 1092787-12-6
-
Peso molecular 348.20
-
Fòrmula C14H14BrN5O
-
SMILES
BrC1=C(O)C=C(C2=NN(C(C)C)C3=C2C(N)=NC=N3)C=C1
-
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)