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Tyrosine Kinase/Adaptors

Tyrosine Kinase/Adaptors

Tyrosine kinase and adaptor inhibitors are compounds that target tyrosine kinases and their associated adaptor proteins, which play pivotal roles in cell signaling, growth, and differentiation. These inhibitors are essential tools in cancer research, as many tyrosine kinases are involved in the signaling pathways that drive tumor growth and metastasis. By inhibiting tyrosine kinases, these compounds can block critical signaling cascades, offering potential therapeutic strategies for various cancers and other diseases involving abnormal cell signaling. At CymitQuimica, we provide a comprehensive range of high-quality tyrosine kinase and adaptor inhibitors to support your research in oncology, molecular biology, and targeted therapy development.

Subcategories of "Tyrosine Kinase/Adaptors"

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Found 1259 products of "Tyrosine Kinase/Adaptors"

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  • LDN-193189 HCl

    CAS:
    LDN-193189 HCl (LDN193189 Hydrochloride) is a selective BMP type I receptor kinases inhibitor.
    Formula:C25H22N6·HCl
    Purity:99.49% - 99.53%
    Color and Shape:Solid
    Molecular weight:442.94
  • (Rac)-JBJ-04-125-02

    CAS:
    (Rac)-JBJ-04-125-02 (JBJ-04-125-02) is effective as a single agent in both in vitro and in vivo models of EGFR-mutant lung cancer.
    Formula:C29H26FN5O3S
    Purity:97.57%
    Color and Shape:Solid
    Molecular weight:543.61
  • Nintedanib

    CAS:
    <p>Nintedanib (Intedanib) is a triple vascular kinase inhibitor that inhibits VEGFR1, VEGFR2, and VEGFR3 (IC50=34/13/13 nM), FGFR1, FGFR2, and FGFR3 (IC50=69/37/</p>
    Formula:C31H33N5O4
    Purity:98% - 99.92%
    Color and Shape:Solid
    Molecular weight:539.62
  • Cyasterone

    CAS:
    Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promising
    Formula:C29H44O8
    Purity:99.32% - 99.70%
    Color and Shape:Solid
    Molecular weight:520.65
  • Leptomycin B

    CAS:
    Leptomycin B: potent CRM1 inhibitor, blocks protein nuclear export and cell cycle, antifungal, modifies cysteine.
    Formula:C33H48O6
    Purity:97.10% - 99.04%
    Color and Shape:White Crystalline Solid
    Molecular weight:540.73
  • Genistein

    CAS:
    <p>Genistein (NPI 031L) is a natural soy isoflavone, a multi-targeted tyrosine kinase inhibitor. Genistein has antitumor effects. Cost effective and quality assured.</p>
    Formula:C15H10O5
    Purity:98.22% - 99.64%
    Color and Shape:Rectangular Or Six-Sided Rods From 60% Alcohol Dendritic Needles From Ether Solid
    Molecular weight:270.24
  • Rostafuroxin

    CAS:
    <p>Rostafuroxin (PST 2238) has been used in trials studying the treatment of Essential Hypertension.</p>
    Formula:C23H34O4
    Purity:99.08% - >99.99%
    Color and Shape:Solid
    Molecular weight:374.51
  • Fenebrutinib

    CAS:
    <p>Fenebrutinib (GDC-0853) is a selective and noncovalent Btk inhibitor (Ki: 0.91 nM).</p>
    Formula:C37H44N8O4
    Purity:98.26% - 98.94%
    Color and Shape:Solid
    Molecular weight:664.8
  • RET V804M-IN-1

    CAS:
    RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).
    Formula:C19H16N6O
    Purity:97.94% - 99.62%
    Color and Shape:Solid
    Molecular weight:344.37
  • Mobocertinib

    CAS:
    Mobocertinib (tak788) is a potent inhibitor of epidermal growth factor receptor (EGFR) and an antineoplastic agent
    Formula:C32H39N7O4
    Purity:99.47% - 99.97%
    Color and Shape:Solid
    Molecular weight:585.7
  • Oclacitinib maleate

    CAS:
    Oclacitinib maleate is a selective JAK inhibitor (IC50: 10-99 nM; JAK1 cytokines: 36-249 nM), with no effect on 38 non-JAK kinases.
    Formula:C15H23N5O2S·C4H4O4
    Purity:99.17% - 99.92%
    Color and Shape:Solid
    Molecular weight:453.51
  • CUDC-101

    CAS:
    CUDC-101 is a potent inhibitor of HDAC, EGFR and HER2 with IC50s of 4.4, 2.4 and 15.7 nM, respectively.
    Formula:C24H26N4O4
    Purity:95.76% - 99.17%
    Color and Shape:Solid
    Molecular weight:434.49
  • BBT594

    CAS:
    <p>BBT594 (NVP-BBT594)(NVP-BBT594) is a potent inhibitor of receptor tyrosine kinase RET,Treatment of cancer.</p>
    Formula:C28H30F3N7O3
    Purity:99.57%
    Color and Shape:Solid
    Molecular weight:569.58
  • DDR1-IN-2

    CAS:
    DDR1-IN-2 (DDR1 inhibitor 7rh) (DDR1 inhibitor 7rh) is a potent, selective, ATP-competitive Discoidin domain receptor 1 (DDR1) inhibitor (IC50: 6.8 nM in cell-
    Formula:C30H29F3N6O
    Purity:97.51%
    Color and Shape:Solid
    Molecular weight:546.59
  • Afatinib

    CAS:
    <p>Afatinib (BIBW 2992) is an irreversible and orally EGFR family inhibitor that inhibits EGFR and HER2. Afatinib has antitumor activity. Cost effective and quality assured.</p>
    Formula:C24H25ClFN5O3
    Purity:98.56% - 99.9%
    Color and Shape:Off-White Solid
    Molecular weight:485.94
  • 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>
    Formula:C33H29F2N5O4S
    Purity:98.9% - 99.85%
    Color and Shape:Solid
    Molecular weight:629.68
  • PD153035

    CAS:
    PD153035 (NSC-669364) hydrochloride is an effective and selective inhibitor of EGFR (Ki/IC50: 5.2/29 pM, in cell-free assays); little inhibitory against FGFR,
    Formula:C16H14BrN3O2
    Purity:98.47% - 99.29%
    Color and Shape:Solid
    Molecular weight:360.21
  • KHS101 hydrochloride

    CAS:
    KHS101 is a TACC3 inhibitor and can selectively induce a neuronal differentiation phenotype.
    Formula:C18H22ClN5S
    Purity:99.6%
    Color and Shape:Solid
    Molecular weight:375.92
  • 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>
    Formula:C21H25N7
    Purity:97.63% - ≥95%
    Color and Shape:Solid
    Molecular weight:375.47
  • Nazartinib

    CAS:
    Nazartinib (EGF816) (EGF816, NVS-816) is a covalent, irreversible, mutant-selective EGFR inhibitor that has nanomolar inhibitory potency against activating mt (
    Formula:C26H31ClN6O2
    Purity:98.63% - ≥95%
    Color and Shape:Solid Powder
    Molecular weight:495.02