GLPBio

PDGFR

PDGFR (platelet-derived growth factor receptor) is a group of cell surface tyrosine kinase receptors for members of the PDGF (platelet-derived growth factor) family.

Products Related to PDGFR(111)

  • GC66385 structure
    GC66385Tovetumab
    CAS: 1243266-04-7
    Purity: >99.00%

    Tovetumab (MEDI-575) es un anti-PDGFRα anticuerpo monoclonal que bloquea selectivamente el PDGFRα transducciÓn de seÑales. Tovetumab se puede utilizar en la investigaciÓn del glioblastoma y el cÁncer de pulmÓn de células no pequeÑas (NSCLC).

  • GC67774 structure
    GC67774CT52923
    CAS: 205256-55-9
    Purity: >98.00%
  • GC69619 structure
    GC69619Olaratumab
    CAS: 1024603-93-7
    Purity: >95.00%

    Olaratumab (IMC-3G3; LY3012207) es un anticuerpo monoclonal humano IgG1 que se dirige al receptor del factor de crecimiento derivado de las plaquetas α (PDGFRα), y tiene actividad antitumoral.

  • GC70992 structure
    GC70992Ansornitinib
    CAS: 1448874-96-1
    Purity: >98.00%

    Ansornitinib es un inhibidor de la quinasa dual activo por vía oral que inhiel receptor del factor de crecimiento derivado de plaquetas (PDGFR) y el receptor del factor de crecimiento endotelial vascular (VEGFR2).

  • GC72911 structure
    GC72911Pazopanib-13C,d3 hydrochloride
    CAS: 1261398-44-0
    Purity: >97.00%

    Pazopanib-13C,d3 hydrochloride es el deuterio y 13C etiquetado Pazopanib droclor.

  • GC73370 structure
    GC73370AXL-IN-13
    CAS: 2376928-82-2
    Purity: >98.00%

    AXL-IN-13 es un potente inhibidor de AXL activo por vía oral (IC50: 1.6 nM, Kd: 0.26 nM).

  • GC81304 structure
    GC81304GW296115
    CAS: 118458-58-5
    Purity: >98.50%

    GW296115 is a multi-target inhibitor with the following IC 50 values against its targets: 8.4 nM for BRSK2, 21 nM for BRSK1, 1.8 μM for PDGFRβ, 5.5 nM for STK17B/DRAK2, 28 nM for DRAK1, 20 nM for PHKG1, and 89 nM for DCAMKL3.

  • GC81305 structure
    GC81305Tyrosine kinase-IN-11
    CAS: 3031972-21-8
    Purity: >98.50%

    Tyrosine kinase-IN-11 (Compound 4b) is a tyrosine kinase inhibitor.

  • GC81321 structure
    GC81321Pegpleranib sodium
    Purity: >98.00%

    Pegpleranib (Fovista) sodium is a pegylated DNA aptamer that selectively binds to PDGF-BB and PDGF-AB homodimers and heterodimers, interrupting the interaction with their associated tyrosine kinase receptors.

  • GC81323 structure
    GC81323PDGFRA/CAIX/XII-IN-1
    Purity: >98.00%

    PDGFRA/CAIX/XII-IN-1 is an inhibitor of PDGFRA, CA IX and CA XII, with an IC 50 of 20 nM against PDGFRA, a K i of 93.3 nM against CA IX, and a K i of 80.0 nM against CA XII.

  • GC81325 structure
    GC81325VEGFR2-IN-84
    CAS: 861877-12-5
    Purity: >98%

    VEGFR2-IN-84 is an orally active, multi-targeted tyrosine kinase inhibitor based on a naphthalene ring scaffold.

  • GC81443 structure
    GC81443E8431
    CAS: 2419580-01-9
    Purity: >97.00%

    E8431 is a DCSTAMP antagonist with an IC 50 value of 775.8 nM for osteoclastogenesis.

  • GC91419 structure
    GC91419CYY292
    CAS: 2644673-04-9
    Purity: >98.00%

    CYY292 es un inhibidor de PDGFRα, PDGFRβ, FGFR1, -2 y -3 (IC50s = 5.35, 4.6, 28, 28 y 78 nM respectivamente).

  • GN10603 structure
    GN10603Sennoside B
    CAS: 128-57-4
    Purity: >99.00%
  • GC17651 structure
    GC17651Sunitinib
    CAS: 557795-19-4
    Purity: >98.00%

    Sunitinib (SU 11248) es un inhibidor de la tirosina quinasa de múltiples objetivos que se toma por vía oral, con valores de IC50 de 80 nM y 2 nM para el receptor del factor de crecimiento endotelial vascular (VEGFR2) y el receptor del factor de crecimiento derivado de plaquetas (PDGFRβ), respectivamente.