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Results for "

VEGFR2 (Flk-1)

" in MedChemExpress (MCE) Product Catalog:

7

Inhibitors & Agonists

18

Recombinant Proteins

2

Antibodies

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-21289

    SU5205 is an inhibitor of VEGFR2 (FLK-1), with an IC50 of 9.6 μM [1].
    SU5205
  • HY-19326
    SU1498
    5 Publications Verification

    AG 1498; Tyrphostin SU 1498

    VEGFR Inflammation/Immunology Cancer
    SU1498 (AG 1498) is a selective inhibitor of the VEGFR2; inhibits Flk-1 with an IC50 of value of 700 nM [1].
    SU1498
  • HY-126319

    VEGFR EGFR Cancer
    SU5204, a tyrosine kinase inhibitor, has IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2, respectively [1].
    SU5204
  • HY-21292

    SU4949

    SU5214 is a potent VEGFR2 inhibitor extracted from patent US5834504A, SU5214, has IC50s of 14.8 µM (FLK-1) and 36.7 µM (EGFR), respectively [1].
    SU5214
  • HY-112337

    VEGFR PDGFR Cancer
    VEGFR-2-IN-44 (compound 4b) is a selective VEGF-R2 (Flk-1) inhibitor with an IC50 value of 70 nM. VEGFR-2-IN-44 also inhibits PDGF-Rβ with an IC50 of 920 nM [1].
    VEGFR-2-IN-44
  • HY-120640

    VEGFR PDGFR Cancer
    BMS-605541 is a selective and orally active inhibitor of VEGFR-2 kinase with an IC50 value of 23 nM and Ki value of 49 nM. BMS-605541 inhibits the activity of Flk-1, VEGFR-1 and PDGFR-β with IC50 values of 40 nM, 400 nM and 200 nM, respectively. BMS-605541 can be used for cancer research [1].
    BMS-605541
  • HY-119757

    SU1433; AG1433

    PDGFR VEGFR Cancer
    Tyrphostin AG1433 (SU1433) is a tyrosine kinases inhibitor. AG1433 is also a selective PDGFRβ and VEGFR-2 (Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively. Tyrphostin AG1433 prevents blood vessel formation [1] [2] .
    Tyrphostin AG1433

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