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Raf

Raf

Las quinasas Raf son componentes clave de la vía de señalización MAPK/ERK, desempeñando un papel crítico en la transmisión de señales desde la membrana celular hasta el núcleo. La activación de Raf conduce a la fosforilación de MEK, que posteriormente activa ERK, influyendo en la división, diferenciación y supervivencia celular. Las mutaciones en Raf, particularmente en B-Raf, están asociadas con varios tipos de cáncer, lo que convierte a Raf en un objetivo crucial en la terapia contra el cáncer. En CymitQuimica, ofrecemos una variedad de inhibidores y moduladores de Raf para apoyar su investigación en oncología, transducción de señales y desarrollo terapéutico.

Se han encontrado 86 productos para "Raf".

productos por página.
  • Anti-Phospho-RAF1 (Ser43) Antibody (8R108)


    Anti-Phospho-RAF1 (Ser43) Antibody (8R108) is an antibody targeting Phospho-RAF1 (Ser43). Anti-Phospho-RAF1 (Ser43) Antibody (8R108) can be used in ELISA, IF.
    Forma y color:Odour Liquid
  • Anti-Phospho-RAF1 (Ser259) Antibody (5X237)


    Anti-Phospho-RAF1 (Ser259) Antibody (5X237) is an antibody targeting Phospho-RAF1 (Ser259). Anti-Phospho-RAF1 (Ser259) Antibody (5X237) can be used in ELISA, WB, IHC, IF.
    Forma y color:Odour Liquid
  • RAS GTPase inhibitor 1 TFA

    CAS:
    RAS GTPase inhibitor 1 TFA is a RAS GTPase inhibitor with potential antitumor activity.
    Fórmula:C27H28ClF4N5O2
    Pureza:98.43%
    Forma y color:Solid
    Peso molecular:565.99
  • K-Ras(G12C) inhibitor 6

    CAS:
    Irreversible K-Ras(G12C) inhibitor 6 fully modifies the protein at 10 μM after 24h in vitro.
    Fórmula:C17H22Cl2N2O3S
    Pureza:89.07% - 97.09%
    Forma y color:Solid
    Peso molecular:405.33
  • Kobe2602

    CAS:
    Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
    Fórmula:C14H9F4N5O4S
    Pureza:98.36% - 99.39%
    Forma y color:Solid
    Peso molecular:419.311
  • GW 5074

    CAS:
    GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor.
    Fórmula:C15H8Br2INO2
    Pureza:99.32%
    Forma y color:Yellow Solid
    Peso molecular:520.94
  • Takeda-6d

    CAS:
    Takeda-6d is a novel, potent DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with IC50 of 7.0 nM and 2.2 nM, respectively.
    Fórmula:C27H19ClFN5O3S
    Pureza:98.27%
    Forma y color:Yellow Solid
    Peso molecular:547.988
  • Ro 5126766

    CAS:
    RO5126766 (CH5126766) is a dual RAF/MEK inhibitor with IC50 of 8.2 nM, 19 nM, 56 nM, and 160 nM for BRAF V600E, BRAF, CRAF, and MEK1, respectively. Phase 1.
    Fórmula:C21H18FN5O5S
    Pureza:98.3% - 98.81%
    Forma y color:White Solid
    Peso molecular:471.462
  • PLX-4720

    CAS:
    PLX-4720 is a potent and selective B-Raf (V600E) inhibitor designed to block the ATP-binding site of oncogenic B-Raf.Cost-effective and quality-assured.
    Fórmula:C17H14ClF2N3O3S
    Pureza:97.78% - 99.96%
    Forma y color:White Solid
    Peso molecular:413.826
  • AZ304

    CAS:
    AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits BRAF (WT), BRAF (V600E), and wild type CRAF (IC50s: 79/38/68 nM).
    Fórmula:C27H25N5O2
    Pureza:99.82%
    Forma y color:Solid
    Peso molecular:451.5197
  • Raf inhibitor 2

    CAS:
    Raf inhibitor 2 (CID 25014542) is novel inhibitor of Raf kinases.
    Fórmula:C15H8Br2ClNO2
    Pureza:98.53%
    Forma y color:White Solid
    Peso molecular:429.491
  • Regorafenib monohydrate

    CAS:
    Regorafenib Monohydrate is a novel oral multikinase inhibitor with IC50 values of 13, 4.2, 46, 22, 7, 1.5, 2.5, 28, 19 nM for VEGFR1, murine VEGFR2, murine
    Fórmula:C21H17ClF4N4O4
    Pureza:99.69%
    Forma y color:Solid
    Peso molecular:500.83
  • PLX8394

    CAS:
    Plixorafenib (PLX8394) is an orally active inhibitor of the serine/threonine protein kinase B-Raf (BRAF) protein.Cost-effective and quality-assured.
    Fórmula:C25H21F3N6O3S
    Pureza:98.75% - >99.99%
    Forma y color:Solid
    Peso molecular:542.533
  • Regorafenib

    CAS:
    Regorafenib (BAY 73-4506) is a multi-targeted receptor tyrosine kinase inhibitor that inhibits RET, C-RAF, VEGFR2, c-Kit, VEGFR1, and PDGFRβ and is orally
    Fórmula:C21H15ClF4N4O3
    Pureza:98% - 99.95%
    Forma y color:Solid
    Peso molecular:482.815
  • ZM 336372

    CAS:
    ZM 336372 is a potent and selective c-Raf inhibitor.
    Fórmula:C23H23N3O3
    Pureza:97.24% - 97.51%
    Forma y color:Solid
    Peso molecular:389.45
  • SB-590885

    CAS:
    SB590885 is an effective B-Raf inhibitor (Ki: 0.16 nM, in a cell-free assay).
    Fórmula:C27H27N5O2
    Pureza:95.42% - 99.06%
    Forma y color:Solid
    Peso molecular:453.5356
  • K-Ras(G12C) inhibitor 9

    CAS:
    K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
    Fórmula:C16H21ClIN3O4S
    Pureza:97.33% - 97.45%
    Forma y color:Solid
    Peso molecular:513.778
  • AD80

    CAS:
    AD80, a multikinase inhibitor, inhibits RET, RAF, SRCand S6K, with greatly reduced mTOR activity.
    Fórmula:C22H19F4N7O
    Pureza:99.49% - 99.75%
    Forma y color:Solid
    Peso molecular:473.4262
  • BI-882370

    CAS:
    BI-882370 is a specific RAF kinase inhibitor.
    Fórmula:C28H33F2N7O2S
    Pureza:97.33% - 99.07%
    Forma y color:Solid
    Peso molecular:569.669
  • RAF709

    CAS:
    RAF709 is a novel Raf kinase inhibitor with IC50s of 0.5 and 1.8 nM for c-Raf and b-Raf, respectively.
    Fórmula:C28H29F3N4O4
    Pureza:99.28% - 99.8%
    Forma y color:White Solid
    Peso molecular:542.5495