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Raf

Raf

Le chinasi Raf sono componenti chiave della via di segnalazione MAPK/ERK, svolgendo un ruolo critico nella trasmissione dei segnali dalla membrana cellulare al nucleo. L'attivazione di Raf porta alla fosforilazione di MEK, che successivamente attiva ERK, influenzando la divisione, la differenziazione e la sopravvivenza cellulare. Le mutazioni in Raf, in particolare in B-Raf, sono associate a vari tipi di cancro, rendendo Raf un bersaglio cruciale nella terapia del cancro. Presso CymitQuimica, offriamo una varietà di inibitori e modulatori di Raf per supportare la tua ricerca in oncologia, trasduzione del segnale e sviluppo terapeutico.

Trovati 82 prodotti di "Raf"

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  • Anti-Phospho-RAF1 (Ser259) Antibody (5X237)


    <p>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.</p>
    Colore e forma:Odour Liquid
  • RAS GTPase inhibitor 1

    CAS:
    RAS GTPase inhibitor 1 is a RAS GTPase inhibitor with potential antitumor activity.
    Formula:C27H28ClF4N5O2
    Purezza:98.43%
    Colore e forma:Solid
    Peso molecolare:565.99
  • 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
    Formula:C21H15ClF4N4O3
    Purezza:98% - 99.95%
    Colore e forma:Solid
    Peso molecolare:482.82
  • PLX8394

    CAS:
    <p>Plixorafenib (PLX8394) is an orally active inhibitor of the serine/threonine protein kinase B-Raf (BRAF) protein.Cost-effective and quality-assured.</p>
    Formula:C25H21F3N6O3S
    Purezza:98.75% - >99.99%
    Colore e forma:Solid
    Peso molecolare:542.53
  • L-779450

    CAS:
    L-779450, an effective, ATP-competitive Raf kinase inhibitor (IC50: 10 nM) , displays >7, >30 and >70-fold selectivity over p38α, GSK3β and Lck respectively.
    Formula:C20H14ClN3O
    Purezza:≥95%
    Colore e forma:Solid
    Peso molecolare:347.8
  • 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.
    Formula:C27H19ClFN5O3S
    Purezza:98.27%
    Colore e forma:Solid
    Peso molecolare:547.99
  • GW 5074

    CAS:
    GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor.
    Formula:C15H8Br2INO2
    Purezza:99.32%
    Colore e forma:Solid
    Peso molecolare:520.94
  • 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.
    Formula:C17H14ClF2N3O3S
    Purezza:97.78% - 99.83%
    Colore e forma:Solid
    Peso molecolare:413.83
  • AZ304

    CAS:
    <p>AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits BRAF (WT), BRAF (V600E), and wild type CRAF (IC50s: 79/38/68 nM).</p>
    Formula:C27H25N5O2
    Purezza:99.82%
    Colore e forma:Solid
    Peso molecolare:451.52
  • Encorafenib

    CAS:
    Encorafenib (LGX818) is an orally available mutated BRaf V600E inhibitor(IC50=0.3 nM) with potential antineoplastic activity.
    Formula:C22H27ClFN7O4S
    Purezza:99.51% - 99.83%
    Colore e forma:Solid
    Peso molecolare:540.01
  • Raf inhibitor 2

    CAS:
    Raf inhibitor 2 (CID 25014542) is novel inhibitor of Raf kinases.
    Formula:C15H8Br2ClNO2
    Purezza:98.53%
    Colore e forma:Solid
    Peso molecolare:429.49
  • Kobe2602

    CAS:
    Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
    Formula:C14H9F4N5O4S
    Purezza:98.36% - 99.39%
    Colore e forma:Solid
    Peso molecolare:419.31
  • Regorafenib monohydrate

    CAS:
    <p>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</p>
    Formula:C21H17ClF4N4O4
    Purezza:99.69%
    Colore e forma:Solid
    Peso molecolare:500.83
  • ZM 336372

    CAS:
    ZM 336372 is a potent and selective c-Raf inhibitor.
    Formula:C23H23N3O3
    Purezza:97.24% - 97.51%
    Colore e forma:Solid
    Peso molecolare:389.45
  • Plx-4032

    CAS:
    Plx-4032 (Vemurafenib) is a small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma.
    Formula:C23H18ClF2N3O3S
    Purezza:98.53% - 99.36%
    Colore e forma:Solid
    Peso molecolare:489.92
  • SB-590885

    CAS:
    SB590885 is an effective B-Raf inhibitor (Ki: 0.16 nM, in a cell-free assay).
    Formula:C27H27N5O2
    Purezza:95.42% - 99.06%
    Colore e forma:Solid
    Peso molecolare:453.54
  • AD80

    CAS:
    AD80, a multikinase inhibitor, inhibits RET, RAF, SRCand S6K, with greatly reduced mTOR activity.
    Formula:C22H19F4N7O
    Purezza:99.49% - 99.75%
    Colore e forma:Solid
    Peso molecolare:473.43
  • K-Ras(G12C) inhibitor 9

    CAS:
    K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
    Formula:C16H21ClIN3O4S
    Purezza:97.33% - 97.45%
    Colore e forma:Solid
    Peso molecolare:513.78
  • BI-882370

    CAS:
    BI-882370 is a specific RAF kinase inhibitor.
    Formula:C28H33F2N7O2S
    Purezza:97.33% - 99.07%
    Colore e forma:Solid
    Peso molecolare:569.67
  • RAF265

    CAS:
    RAF265 (CHIR-265) inhibits C-Raf/B-Raf/V600E (IC50: 3-60 nM), blocks VEGFR2 (EC50: 30 nM), in Phase 2 trials.
    Formula:C24H16F6N6O
    Purezza:99.56%
    Colore e forma:Solid
    Peso molecolare:518.41