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EGFR

EGFR

Los inhibidores del receptor del factor de crecimiento epidérmico (EGFR) son compuestos que bloquean la señalización del EGFR, un receptor que a menudo está sobreexpresado en varios tipos de cáncer y que juega un papel crucial en la angiogénesis. Los inhibidores del EGFR se utilizan para prevenir el crecimiento tumoral y las metástasis al interrumpir las vías que promueven la formación de vasos sanguíneos en los tumores. Estos inhibidores son ampliamente utilizados en la investigación y terapia contra el cáncer. En CymitQuimica, ofrecemos una amplia selección de inhibidores de EGFR de alta calidad para apoyar su investigación en oncología y angiogénesis.

Se han encontrado 594 productos de "EGFR"

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  • Desmethyl Erlotinib hydrochloride

    CAS:
    <p>Desmethyl Erlotinib hydrochloride (OSI 420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor.</p>
    Fórmula:C21H21N3O4·HCl
    Pureza:99.49%
    Forma y color:Solid
    Peso molecular:415.87
  • RG14620

    CAS:
    <p>RG14620 (Tyrphostin RG14620) is an epidermal growth factor receptor (EGFR) inhibitor.</p>
    Fórmula:C14H8Cl2N2
    Pureza:99.82% - 99.87%
    Forma y color:Solid
    Peso molecular:275.13
  • AG490

    CAS:
    AG490 inhibits EGFR (0.1 μM IC50), 135x > selective than ErbB2, blocks JAK2, spares Lyn, Lck, Syk, Btk, Src.
    Fórmula:C17H14N2O3
    Pureza:98.6% - 99.85%
    Forma y color:Yellow Solid
    Peso molecular:294.3
  • RG13022

    CAS:
    RG13022 (Tyrphostin RG13022) is a tyrosine kinase inhibitor; inhibits the autophosphorylation reaction of the EGF receptor (IC50: 4 μM).
    Fórmula:C16H14N2O2
    Pureza:98.38%
    Forma y color:Solid
    Peso molecular:266.29
  • TAS6417

    CAS:
    Zipalertinib (TAS6417, CLN-081) is a novel, highly potent, orally active covalent EGFR tyrosine kinase inhibitor.Cost-effective and quality-assured.
    Fórmula:C23H20N6O
    Pureza:99.71%
    Forma y color:Solid
    Peso molecular:396.44
  • Epitinib

    CAS:
    <p>Epitinib is an orally active, selective, blood-brain barrier crossing epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI).</p>
    Fórmula:C24H26N6O2
    Forma y color:Solid
    Peso molecular:430.5
  • Chrysophanol

    CAS:
    Chrysophanol (Turkey Rhubarb) is an EGFR/mTOR pathway inhibitor, which can be found in rhubarb, and sorrel.
    Fórmula:C15H10O4
    Pureza:99.44% - 99.91%
    Forma y color:Physical Description Golden Yellow Plates Or Brown Powder Melting Point 196°C
    Peso molecular:254.24
  • Theliatinib tartrate

    CAS:
    Theliatinib: oral EGFR blocker, Ki 0.05 nM, IC50 3 nM (wild-type), 22 nM (T790M/L858R), >50x kinase selectivity.
    Fórmula:C29H32N6O8
    Forma y color:Solid
    Peso molecular:592.6
  • Tuxobertinib

    CAS:
    Tuxobertinib (BDTX-189) is a potent and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations. BDTX-189 exhibits anticancer activity.
    Fórmula:C29H29ClN6O4
    Pureza:99.22%
    Forma y color:Solid
    Peso molecular:561.03
  • PD153035 hydrochloride

    CAS:
    <p>PD153035 hydrochloride (ZM 252868) is a effective and selective inhibitor of EGFR; few influence against FGFR, PGDFR, InsR, CSF-1, and Src.</p>
    Fórmula:C16H15BrClN3O2
    Pureza:99.39% - ≥95%
    Forma y color:Solid
    Peso molecular:396.67
  • Neratinib

    CAS:
    Neratinib (HKI-272) (HKI-272) is an orally available, irreversible tyrosine kinase inhibitor for HER2 and EGFR (IC50: 59/92 nM), respectively.
    Fórmula:C30H29ClN6O3
    Pureza:96.17% - 99.85%
    Forma y color:Solid
    Peso molecular:557.04
  • Mutant EGFR inhibitor

    CAS:
    Selective, potent inhibitor for mutated EGFR: L858R, Exon19 deletion, T790M resistance mutants.
    Fórmula:C27H30ClN7O2
    Pureza:98% - 99.75%
    Forma y color:Solid
    Peso molecular:520.03
  • Osimertinib mesylate

    CAS:
    <p>Osimertinib mesylate (AZD-9291 mesylate) is an EGFR third-generation inhibitor. Osimertinib mesylate has antitumor activity. Cost-effective and quality-assured.</p>
    Fórmula:C29H37N7O5S
    Pureza:99.46% - >99.99%
    Forma y color:Solid
    Peso molecular:595.71
  • Mubritinib

    CAS:
    Mubritinib (TAK-165) (TAK-165) is a potent inhibitor of HER2/ErbB2 with IC50 of 6 nM.
    Fórmula:C25H23F3N4O2
    Pureza:98.61% - 99.85%
    Forma y color:Solid
    Peso molecular:468.47
  • Oritinib mesylate

    CAS:
    Oritinib mesylate (SH-1028), an oral pyrimidine EGFR blocker with 18 nM IC50, targets both sensitive and T790M resistant mutations.
    Fórmula:C32H41N7O5S
    Forma y color:Solid
    Peso molecular:635.78
  • WS6

    CAS:
    WS6, a β cell proliferation inducer, regulates Erb3 binding protein-1 (EBP1) and the IκB kinase pathway.
    Fórmula:C29H31F3N6O3
    Pureza:97.65% - 99.95%
    Forma y color:Solid
    Peso molecular:568.59
  • BI-4020

    CAS:
    <p>BI-4020 is a fourth-generation, orally active, and non-covalent inhibitor of EGFR tyrosine kinase.</p>
    Fórmula:C30H38N8O2
    Pureza:97.21% - >99.99%
    Forma y color:Solid
    Peso molecular:542.68
  • PD158780

    CAS:
    PD 158780 blocks all ErbB receptors: EGFR, ErbB2-4, with IC50s: 8μM, 49-52 nM.
    Fórmula:C14H12BrN5
    Pureza:98.81%
    Forma y color:Solid
    Peso molecular:330.18
  • (E)-AG 556

    CAS:
    <p>AG 556 is a selective inhibitor of EGFR and blocks LPS-induced TNF-α production.</p>
    Fórmula:C20H20N2O3
    Pureza:99.93%
    Forma y color:Light Yellow Powder
    Peso molecular:336.38
  • SU5214

    CAS:
    SU5214 is a modulator of tyrosine kinase signal transduction.
    Fórmula:C16H13NO2
    Pureza:99.45% - 99.55%
    Forma y color:Solid
    Peso molecular:251.28