Home   >  
Angiogenesis/Protein Tyrosine Kinase
  >  
VEGFR

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

VEGFR

Chemical Structure Cat. No. Product Name CAS No.
Bevacizumab Chemical Structure
BCP07998 Bevacizumab 216974-75-3
Bevacizumab is a recombinant humanized monoclonal antibody that blocks angiogenesis by inhibiting vascular endothelial growth factor A (VEGF-A).
AAL-993 Chemical Structure
BCP18097 AAL-993 269390-77-4
AAL-993 is a highly potent inhibitor of VEGFR-1 (IC50 =130nM), VEGFR-2 (IC50=23nM) and VEGFR-3 (IC50=18nM).
ODM-203 Chemical Structure
BCP30030 ODM-203 1430723-35-5
ODM-203 is an orally available inhibitor of the human vascular endothelial growth factor receptors (VEGFRs) and fibroblast growth factor receptors (FGFRs), with potential antiangiogenic and antineoplastic activities.
AST-487 Chemical Structure
BCP21589 AST-487 630124-46-8
AST 487 is a RET kinase inhibitor with IC50 of 880 nM, inhibits RET autophosphorylation and activation of downstream effectors, also inhibits Flt-3 with IC50 of 520 nM.
SU-5408 Chemical Structure
BCP29247 SU-5408 15966-93-5
SU5408 is a potent and cell-permeable inhibitor of VEGFR2 kinase with an IC50 of 70 nM.
Oglufanide Chemical Structure
BCP13098 Oglufanide 38101-59-6
Oglufanide inhibits vascular endothelial growth factor (VEGF), which may inhibit angiogenesis.
2-D08 Chemical Structure
BCP18314 2-D08 144707-18-6
2-D08 is a cell permeable, mechanistically unique inhibitor of protein sumoylation.
Ectoine Chemical Structure
BCP14520 Ectoine 96702-03-3
Ectoine is an inhibitor of protein misfolding. It acts by significantly down-regulating Syp, Mapk3 and Tnfα and up-regulating Vegf in rat's hippocampus, prohibiting insulin amyloid formation in vitro.
N-Desethyl Sunitinib Chemical Structure
BCP20914 N-Desethyl Sunitinib 356068-97-8
N-Desethyl Sunitinib is a metabolite of sunitinib.
BMS817378 Chemical Structure
BCP15910 BMS817378 1174161-69-3
BMS-817378 is a potent ATP competitive inhibitor of Met/VEGFR2 with IC50: 1.7 nM/15 nM for Met/VEGFR2.
123下一页末页共 104 条记录 1 / 11 页 
0086-13720134139