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Cat. No. Product Name Information
PC-45746

Fruquintinib

VEGFR inhibitor

Fruquintinib (HMPL-013) is a potent and highly selective small molecule inhibitor of VEGFR1/2/3 with IC50 of 33/3/5/0.5 nM, respectively.
PC-42762

Lenvatinib

VEGFR inhibitor

Lenvatinib (E7080) is a multitargeted kinase inhibitor with IC50s of 4/5.2/22/46 nM for VEGFR2/VEGFR3/VEGFR1/FGFR1 in cell free assays.
PC-42450

Cediranib

VEGFR inhibitor

Cediranib (AZD2171) is a highly potent, orally bioavailable, pan-VEGFR inibitor with IC50 of 1, 5, 3 nM for VEGFR1, 2, 3, respectively.
PC-42759

Tivozanib

VEGFR inhibitor

Tivozanib (AV951) is a highly potent inhibitor of pan-VEGFR with IC50s of 60/6.5/15 nM for VEGFR1/2/3.
PC-42534

Brivanib (BMS540215)

VEGFR2/FGFR1 inhibitor

Brivanib (BMS540215) is a potent, dual inhibitor of VEGFR2 and FGFR1 with IC50 of 25 nM and 148 nM respectively.
PC-42623

SU14813 maleate

Multikinase inhibitor

SU14813 maleate is a broad-spectrum RTKs inhibitor with IC50 ranging from 2 to 50 nM for VEGFR-1, VEGFR-2, PDGFRs, KIT, FLT3, and CSF1R/FMS.
PC-42622

SU14813

Multikinase inhibitor

SU14813 is a potent, broad-spectrum RTKs inhibitor with IC50 ranging from 2 to 50 nM for VEGFR-1, VEGFR-2, PDGFRs, KIT, FLT3, and CSF1R/FMS.
PC-23466

ZM-306416

VEGFR inhibitor

ZM-306416 (CB 676475) is a potent inhibitor of VEGFR with IC50 of 0.1 μM and 2 μM for KDR and Flt, respectively, also inhibits EGFR with IC50 of <10 nM.
PC-23424

MAZ51

VEGFR-3 inhibitor

MAZ51 is a specific inhibitor of VEGFR-3, blocks the ligand-induced autophosphorylation of VEGFR-3 and inhibits the proliferation of VEGFR-3-expressing cancer cells.
PC-22874

TU2218

ALK5/VEGFR2 inhibitor

TU2218 is a small-molecule inhibitor that inhibits dual ALK5/VEGFR2 with IC50 of 1.2 nM and 4.5 nM respectively.
PC-21859

Axitinib

VEGFR inhibitor

Axitinib (AG-013736) is a potent, multi-targeted tyrosine kinase inhibitor with IC50 of 0.1, 0.2, 0.1-0.3, 1.6 nM for VEGFR1, VEGFR2, VEGFR3 and PDGFRβ, respectively.
PC-21447

NRPa-308

NRP1 inhibitor

NRPa-308 is a neuropilin-1 (NRP-1) antagonist, inhibits the VEGF-A165/NRP-1 binding with IC50 of 42 uM, exerts in vitro anti-angiogenic activity.

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