JK-P3 T4425
Specifications
| 1mg/5mg/10mg/25mg/50mg/100mg |
Bioactivity:
JK-P3 is a pyrazole-based inhibitor of VEGFR-2 (IC50: 7.8 _M). JK-P3 inhibits FGFR 1/3 kinase activity in vitro, but has no effect on FGFR signaling in cell-based assays. The compound blocks wound healing and tube formation in HUVEC without effecting endo
CAS nr:
942655-44-9
Purity:
98%
Molecular Weight:
323,35
SMILES:
COc1c(cc(cc1)C(=O)Nc1n[nH]c(c1)c1ccccc1)OC
Formula:
C18H17N3O3
Pathway:
Tyrosine Kinase/Adaptors,Angiogenesis
Target:
VEGFR,VEGFR
