NVP-BHG712 is an oral active EphB4 kinase autophosphorylation inhibitor, with IC50 values of 3.3 nM and 3.0 nM for EphA2 and EphB4, respectively.
性状
Solid
IC50 & Target[1][2]
IC50: 3.3 nM (EphA2), 3 nM (EphB4).
体外研究(In Vitro)
NVP-BHG712 inhibits VEGF driven vessel formation, while it has only little effects on VEGF receptor (VEGFR) activity. The data suggests a close cross talk between the VEGFR and EphR signaling during vessel formation.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
NVP-BHG712 (3, 10 and 30 mg/kg, p.o., daily) inhibits VEGF driven tissue growth and angiogenesis.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Mice arrying chambers.
Dosage:
3, 10 and 30 mg/kg.
Administration:
P.O. daily for 4 days.
Result:
Significantly inhibited VEGF stimulated tissue formation and vascularization at doses of daily 3 mg/kg. Administration of 10 mg/kg/kg p.o. was sufficient to reverse VEGF enhanced tissue formation and vessel growth.