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FAK

FAK

FAK (focal adhesion kinase) inhibitors target FAK, a kinase involved in cell adhesion, migration, and angiogenesis. FAK is frequently overexpressed in tumors and contributes to the formation of new blood vessels that supply nutrients to the tumor. Inhibiting FAK can disrupt these processes, making FAK inhibitors valuable tools in cancer therapy and angiogenesis research. At CymitQuimica, we provide a comprehensive range of high-quality FAK inhibitors to support your research in cell biology, cancer, and angiogenesis.

Found 72 products of "FAK"

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  • NVP-TAE 226

    CAS:
    <p>NVP-TAE 226: Potent FAK inhibitor, IC50=5.5nM, stronger vs Pyk2, IC50=3.5nM, weaker against IGF-1R, InsR, c-Met, ALK.</p>
    Formula:C23H25ClN6O3
    Purity:98.07% - 98.78%
    Color and Shape:Solid
    Molecular weight:468.94
  • PF-562271 besylate

    CAS:
    <p>PF-562271 besylate: potent, ATP-competitive FAK inhibitor, IC50 1.5 nM, 10x less effective on Pyk2, highly selective vs other kinases.</p>
    Formula:C21H20F3N7O3S·C6H6O3S
    Purity:97.65% - 99.01%
    Color and Shape:Solid
    Molecular weight:665.66
  • PND-1186

    CAS:
    <p>PND-1186 (VS-4718) is a reversible and specific FAK inhibitor (IC50: 1.5 nM).</p>
    Formula:C25H26F3N5O3
    Purity:99.14% - 99.75%
    Color and Shape:Solid
    Molecular weight:501.5
  • CEP-37440

    CAS:
    <p>CEP-37440 is an effective and specific Dual FAK/ALK inhibitor with IC50s of 120 nM(ALK cellular in 75% human plasma) and 2.3 nM (FAK).</p>
    Formula:C30H38ClN7O3
    Purity:98.86% - 99.98%
    Color and Shape:Solid
    Molecular weight:580.12
  • PF-562271

    CAS:
    <p>PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).</p>
    Formula:C21H20F3N7O3S
    Purity:97.17% - >99.99%
    Color and Shape:Solid
    Molecular weight:507.49
  • FAK activator 1

    CAS:
    <p>ZINC40099027 is a FAK activator that induces gastric mucosal repair in persistent aspirin-associated gastric injury.</p>
    Formula:C23H26F3N3O3
    Purity:99.19%
    Color and Shape:Soild
    Molecular weight:449.47
  • Y 11

    CAS:
    <p>focal adhesion kinase (FAK) inhibitor</p>
    Formula:C8H17BrN4O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:265.15
  • FAK-IN-8

    CAS:
    <p>FAK-IN-8 (compound 5h), a FAK inhibitor with an IC50 of 5.32 μM, exhibits potent anti-proliferative activity, making it suitable for use in cancer research [1].</p>
    Formula:C15H9Cl2N3O2S
    Color and Shape:Solid
    Molecular weight:366.22
  • TG53

    CAS:
    <p>TG53 is a tissue transglutaminase (TG2) and fibronectin (FN) protein-protein interaction inhibitor.</p>
    Formula:C21H22ClN5O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:411.88
  • FLT3-IN-17

    CAS:
    <p>FLT3-IN-17: FAK inhibitor, IC50 of 12 nM; blocks CYPs, FLT3 mutants; IC50 &lt;0.5 nM for D835Y in cancer studies.</p>
    Formula:C23H24N6O2S2
    Color and Shape:Solid
    Molecular weight:480.61
  • ProMMP-9 inhibitor-3c

    CAS:
    <p>ProMMP-9 inhibitor-3c hinders MMP-9 homodimers, blocks proMMP-9/α4β1 integrin/CD44 binding, and detaches EGFR.</p>
    Formula:C18H20FN3O2S
    Color and Shape:Solid
    Molecular weight:361.43
  • FAK inhibitor 5

    CAS:
    <p>FAK inhibitor 5 is a novel allosteric FAK inhibitor, with IC50 values in the low micromolar range.</p>
    Formula:C20H21N3O2S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:367.46
  • NAMI-A

    CAS:
    <p>NAMI-A is a ruthenium-based compound with selective activity against tumor metastasis.NAMI-A inhibits cancer cell adhesion and migration.</p>
    Formula:C8H15Cl4N4ORuS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:458.18
  • FAK inhibitor 2

    CAS:
    <p>FAK inhibitor 2, antitumor and anti-angiogenesis activitiesis ,is a potent focal adhesion kinase (FAK) inhibitor with an IC50 of 0.07 nM .</p>
    Formula:C29H33F3N8O2S2
    Color and Shape:Solid
    Molecular weight:646.75
  • Adhesamine

    CAS:
    <p>Adhesamine, a dumbbell molecule, enhances cell adhesion, growth, neuron differentiation, and survival via MAPK/FAK.</p>
    Formula:C24H32Cl4N8O2S2
    Color and Shape:Solid
    Molecular weight:670.51
  • Defactinib hydrochloride

    CAS:
    <p>Defactinib hydrochloride (PF 04554878 hydrochloride) is a novel inhibitor of FAK.</p>
    Formula:C20H22ClF3N8O3S
    Purity:98.06% - 98.78%
    Color and Shape:Solid
    Molecular weight:546.95
  • Conteltinib

    CAS:
    <p>Conteltinib (CT-707) is an enzyme inhibitor with antitumor activity targeting FAK, ALK and Pyk2. It can be used to study lymphoma.</p>
    Formula:C32H45N9O3S
    Purity:98.12% - 99.54%
    Color and Shape:Solid
    Molecular weight:635.82
  • Roslin 2 bromide

    CAS:
    <p>Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5.</p>
    Formula:C13H19BrN4
    Purity:99.34%
    Color and Shape:Solid
    Molecular weight:311.22
  • FC 11

    CAS:
    <p>FC 11 is a reversible FAK PROTAC Degrader with DC50 of 40-370 pM and degrades pFAKtyr397 in TM3 cells within 3 hours at 100 nM.</p>
    Formula:C41H42F3N13O9S
    Color and Shape:Solid
    Molecular weight:949.91
  • Ifebemtinib

    CAS:
    <p>Ifebemtinib (BI-853520) is an adhesion plaque kinase inhibitor with anti-tumour activity for the study of breast cancer.</p>
    Formula:C28H28F4N6O4
    Purity:98.84% - 99.85%
    Color and Shape:Solid
    Molecular weight:588.55