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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 1375 products of "Tyrosine Kinase/Adaptors"

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  • 4-[(4-Methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamide

    CAS:
    Formula:C29H31N7O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:493.6027

    Ref: IN-DA00350H

    1g
    25.00€
    5g
    33.00€
    10g
    56.00€
    1kg
    506.00€
    25g
    61.00€
    5kg
    To inquire
    100g
    164.00€
    10kg
    To inquire
    500g
    687.00€
  • Lanraplenib

    CAS:
    <p>Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases.</p>
    Formula:C23H25N9O
    Purity:98.35%
    Color and Shape:Solid
    Molecular weight:443.5
  • Duligotuzumab

    CAS:
    <p>Duligotuzumab is a dual-targeting anti-EGFR/HER3 mAb that blocks signaling and induces ADCC for tumors with poor prognosis.</p>
    Purity:95% - 95%
    Color and Shape:Liquid
  • BLU-945

    CAS:
    <p>BLU-945 is a reversible, potent, highly selective, and orally available epidermal growth factor receptor tyrosine kinase inhibitor (TKIs).Cost-effective and quality-assured.</p>
    Formula:C28H37FN6O3S
    Purity:99.11% - 99.16%
    Color and Shape:Solid
    Molecular weight:556.7
  • MS9427

    CAS:
    <p>MS9427: PROTAC EGFR degrader, 7.1 nM (WT), 4.3 nM (L858R); targets mutant via UPS and autophagy; inhibits NSCLC cell growth; anticancer research.</p>
    Formula:C48H58ClFN8O12
    Color and Shape:Solid
    Molecular weight:993.47
  • DSPE-PEG2000-GE11


    <p>DSPE-PEG2000-GE11 is a PEG compound composed of DSPE and an EGFR-targeting peptide (GE11). GE11 is applicable for cancer cells that overexpress EGFR. DSPE-PEG2000-GE11 is utilized in drug delivery.</p>
    Color and Shape:Odour Solid
  • Compound TPX-0046

    CAS:
    <p>Compound TPX-0046 is an inhibitor of RET. Compound TPX-0046 can inhibit the RET autophosphorylation. Compound TPX-0046 can be used for the research of cancer.</p>
    Formula:C21H21FN6O3
    Purity:99.94%
    Color and Shape:Soild
    Molecular weight:424.43
  • CREBtide

    CAS:
    <p>CREBtide is a synthetic substrate for PKA (Km=3.9 µM), which is based on the phosphorylation sequence in d-CREB (cAMP response element binding protein).</p>
    Formula:C73H129N29O19
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1716.99
  • Cixutumumab

    CAS:
    <p>Cixutumumab (IMC-A12), a humanized monoclonal antibody targeting IGF-1R, exhibits high affinity and inhibits ligand-dependent receptor activation, impeding</p>
    Purity:98.5% (SDS-PAGE); 97.5% (SEC-HPLC) - 98.5% (SDS-PAGE); 97.5% (SEC-HPLC)
    Color and Shape:Liquid
  • HER2/neu (654-662) GP2

    CAS:
    <p>Phage display selected Affibody ligands for HER2/neu from a protein library based on a 58-residue Staphylococcal protein A Z domain.</p>
    Formula:C42H77N9O11
    Purity:98%
    Color and Shape:Solid
    Molecular weight:884.11
  • JBJ-09-063 TFA


    <p>JBJ-09-063 TFA, an EGFR inhibitor selective for EGFR mutations, IC50s: 0.147-0.396 nM, blocks EGFR/Akt/ERK signaling, for EGFR-mutant lung cancer research.</p>
    Formula:C33H30F4N4O5S
    Color and Shape:Solid
    Molecular weight:670.67
  • KYL peptide

    CAS:
    <p>EphA4 inhibitor, Kd 0.8 μM, blocks EphA4-EphrinA5; avoids AβO damage, preserves spines &amp; LTP; long half-life (8-12h), neuroprotective.</p>
    Formula:C74H108N14O17
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1465.75
  • EGFR-IN-76

    CAS:
    <p>EGFR-IN-76 is a potent EGFR inhibitor.</p>
    Formula:C30H30ClFN6O2
    Purity:97.02% - 97.72%
    Color and Shape:Solid
    Molecular weight:561.05
  • HER2-IN-14

    CAS:
    <p>HER2-IN-14 (Compound 34) is a potent inhibitor of HER2, achieving an inhibitory concentration (IC50) of 18 nM.</p>
    Formula:C26H23ClF2N8O3
    Color and Shape:Solid
    Molecular weight:568.96
  • PROTAC EGFR degrader 2


    <p>Potent PROTAC EGFR degrader 2; IC50: 4.0 nM, DC50: 36.51 nM; inhibits cell growth; for NTR-responsive synthesis.</p>
    Formula:C58H72ClFN12O8S
    Color and Shape:Solid
    Molecular weight:1151.78
  • Nuzefatide

    CAS:
    <p>Nuzefatide is a peptide that binds to liver protein receptors.</p>
    Formula:C105H162N32O27S3
    Color and Shape:Solid
    Molecular weight:2400.80
  • Valanafusp alfa

    CAS:
    <p>Valanafusp alfa (AGT-181) is a fusion protein targeting HIR and IDUA for MPS I research.</p>
    Color and Shape:Liquid
  • BMS-599626 2HCL(714971-09-2 Free base)

    CAS:
    <p>BMS-599626 2HCL (AC480 2HCl) is a BMS-599626 derivative.</p>
    Formula:C27H29Cl2FN8O3
    Purity:99.11%
    Color and Shape:Odour Solid
    Molecular weight:603.47
  • CRB-0089


    <p>CRB-0089 is a human monoclonal antibody targeting NGF/bNGF. It is used in the study of analgesia.</p>
    Color and Shape:Odour Liquid
  • Necitumumab

    CAS:
    <p>Necitumumab (IMC-11F8) is a human monoclonal antibody against EGFR, an anti-angiogenic agent used in the treatment of advanced non-small cell lung cancer.</p>
    Purity:97.9% (SDS-PAGE); 99.1% (SEC-HPLC) - 97.9% (SDS-PAGE); 99.1% (SEC-HPLC)
    Color and Shape:Liquid
    Molecular weight:145.5 kDa