CymitQuimica logo
VEGFR

VEGFR

Los inhibidores del receptor del factor de crecimiento endotelial vascular (VEGFR) son compuestos que bloquean la señalización del VEGFR, un receptor clave en la vía del VEGF, crucial para la angiogénesis. Los inhibidores del VEGFR impiden la formación de nuevos vasos sanguíneos que suministran nutrientes y oxígeno a los tumores, inhibiendo así el crecimiento tumoral. Estos inhibidores se utilizan ampliamente en la terapia contra el cáncer y en la investigación para estudiar los mecanismos de la angiogénesis y desarrollar tratamientos anticancerígenos. En CymitQuimica, ofrecemos una gama completa de inhibidores de VEGFR de alta calidad para apoyar su investigación en oncología, biología vascular y angiogénesis.

Se han encontrado 262 productos de "VEGFR"

Ordenar por

Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
productos por página.
  • Dovitinib lactate

    CAS:
    <p>Dovitinib lactate (TKI-258 lactate)(TKI258) lactate is a potent inhibitor of fibroblast growth factor receptor 3 (FGFR3) (IC50 :5 nM).</p>
    Fórmula:C24H27FN6O4
    Pureza:99.54% - 99.77%
    Forma y color:Solid
    Peso molecular:482.51
  • AAL-993

    CAS:
    <p>AAL-993: VEGFR inhibitor; IC50: 130 nM (1), 23 nM (2), 18 nM (3); weak on other tyrosine kinases; antiangiogenic &amp; antitumor.</p>
    Fórmula:C20H16F3N3O
    Pureza:99.65%
    Forma y color:Solid
    Peso molecular:371.36
  • RAF265

    CAS:
    <p>RAF265 (CHIR-265) inhibits C-Raf/B-Raf/V600E (IC50: 3-60 nM), blocks VEGFR2 (EC50: 30 nM), in Phase 2 trials.</p>
    Fórmula:C24H16F6N6O
    Pureza:99.56%
    Forma y color:Solid
    Peso molecular:518.41
  • NVP-BAW2881

    CAS:
    NVP-BAW2881 (BAW2881) is a potent and selective VEGFR inhibitor with activity to inhibit chronic and acute skin inflammation.
    Fórmula:C22H15F3N4O2
    Pureza:98.19% - 99.97%
    Forma y color:Solid
    Peso molecular:424.38
  • SU5205

    CAS:
    <p>SU5205 is a VEGFR2 inhibitor.</p>
    Fórmula:C15H10FNO
    Pureza:99.62% - 99.67%
    Forma y color:Solid
    Peso molecular:239.24
  • Foretinib

    CAS:
    <p>Foretinib (GSK1363089) is a broad-spectrum tyrosine kinase inhibitor with IC50s of 0.4 nM and 0.9 nM for Met and KDR.</p>
    Fórmula:C34H34F2N4O6
    Pureza:98.07% - 99.68%
    Forma y color:Solid
    Peso molecular:632.65
  • Vorolanib

    CAS:
    <p>Vorolanib (X-82) is an orally active VEGFR/PDGFR dual inhibitor.</p>
    Fórmula:C23H26FN5O3
    Pureza:97.35%
    Forma y color:Solid
    Peso molecular:439.48
  • Fruquintinib

    CAS:
    <p>Fruquintinib (HMPL-013) is an orally available, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFRs), with potential anti-</p>
    Fórmula:C21H19N3O5
    Pureza:98.84% - 99.89%
    Forma y color:Solid
    Peso molecular:393.39
  • Orantinib

    CAS:
    <p>Orantinib (NSC 702827) , a excellent effective against PDGFR autophosphorylation with Ki of 8 nM, also highly inhibits Flk-1 and FGFR1 trans-phosphorylation.</p>
    Fórmula:C18H18N2O3
    Pureza:98.92% - 99.52%
    Forma y color:Solid
    Peso molecular:310.35
  • AG-13958

    CAS:
    <p>AG-13958 (AG-013958) (AG-013958), a potent VEGFR tyrosine kinase inhibitor, for the treatment of age-related macular degeneration.</p>
    Fórmula:C26H22FN7O
    Pureza:99.4%
    Forma y color:Solid
    Peso molecular:467.5
  • Motesanib

    CAS:
    <p>Motesanib (AMG 706) orally blocks VEGFR, PDGFR, Kit, Ret; curbing angiogenesis and cancer cell growth.</p>
    Fórmula:C22H23N5O
    Pureza:98% - 99.09%
    Forma y color:Solid
    Peso molecular:373.45
  • SKLB1002

    CAS:
    <p>SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM.</p>
    Fórmula:C13H12N4O2S2
    Pureza:98.51% - >99.99%
    Forma y color:Solid
    Peso molecular:320.39
  • Midostaurin

    CAS:
    <p>PKC412(Midostaurin (PKC412); CGP41231; CGP41251) is a broad spectrum protein kinase inhibitor.</p>
    Fórmula:C35H30N4O4
    Pureza:97.61% - >99.99%
    Forma y color:Solid
    Peso molecular:570.64
  • Dovitinib

    CAS:
    <p>Dovitinib is an orally active, multi-targeted tyrosine kinase (RTK) inhibitor with anti-tumor effects.Cost-effective and quality-assured.</p>
    Fórmula:C21H21FN6O
    Pureza:99.35% - 99.92%
    Forma y color:Solid
    Peso molecular:392.43
  • ODM-203

    CAS:
    <p>ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor Immunity</p>
    Fórmula:C26H21F2N5O2S
    Pureza:99.85%
    Forma y color:Solid
    Peso molecular:505.54
  • Sitravatinib

    CAS:
    <p>Sitravatinib (MGCD516) (MGCD516) is an inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Met, c-Kit, PDGFRα/β, PDGFR, and</p>
    Fórmula:C33H29F2N5O4S
    Pureza:98.9% - 99.85%
    Forma y color:Solid
    Peso molecular:629.68
  • 4SC-203

    CAS:
    <p>4SC-203 is a multi-kinase inhibitor with potential anti-tumor activity.Cost-effective and quality-assured.</p>
    Fórmula:C33H38N8O4S
    Pureza:96.4% - 99.67%
    Forma y color:Solid
    Peso molecular:642.77
  • hVEGF-IN-1

    CAS:
    <p>hVEGF-IN-1 inhibits human VEGF-A translation and has antitumor activity.</p>
    Fórmula:C34H43N7O2
    Pureza:99.76% - >99.99%
    Forma y color:Solid
    Peso molecular:581.75
  • ENMD-2076

    CAS:
    <p>ENMD-2076, a multi-targeted kinase inhibitor, has specific activity against Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα.</p>
    Fórmula:C21H25N7
    Pureza:97.63% - ≥95%
    Forma y color:Solid
    Peso molecular:375.47
  • SPHINX31

    CAS:
    <p>SPHINX31 is a potent inhibitor of serine/arginine-rich protein kinase 1 (SRPK1; IC50: 5.9 nM).</p>
    Fórmula:C27H24F3N5O2
    Pureza:98.81% - 99.3%
    Forma y color:Solid
    Peso molecular:507.51