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EGFR

EGFR

Gli inibitori del recettore del fattore di crescita epidermico (EGFR) sono composti che bloccano la segnalazione dell'EGFR, un recettore spesso sovraespresso in vari tipi di cancro e che svolge un ruolo cruciale nell'angiogenesi. Gli inibitori dell'EGFR sono utilizzati per prevenire la crescita tumorale e le metastasi interrompendo le vie che promuovono la formazione di vasi sanguigni nei tumori. Questi inibitori sono ampiamente utilizzati nella ricerca e nella terapia del cancro. Presso CymitQuimica, offriamo una vasta selezione di inibitori dell'EGFR di alta qualità per supportare la tua ricerca in oncologia e angiogenesi.

Trovati 594 prodotti di "EGFR"

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  • EGFR-IN-68

    CAS:
    EGFR-IN-68, an EGFR inhibitor, has an IC50 of 0.33 μM and shows significant anticancer effects.
    Formula:C24H22N2O
    Colore e forma:Solid
    Peso molecolare:354.44
  • DBPR112

    CAS:
    DBPR112: oral furanopyrimidine EGFR inhibitor; IC50: 15 nM (EGFRWT), 48 nM (L858R/T790M); blocks ATP site, strong antitumor effects.
    Formula:C32H31N5O3
    Purezza:99.25%
    Colore e forma:Solid
    Peso molecolare:533.62
  • BKI-1369

    CAS:
    BKI-1369 is a bumped kinase inhibitor. BKI-1369 increases hERG-inhibitory activity (IC50:1.52 μM).
    Formula:C23H27N7O
    Colore e forma:Solid
    Peso molecolare:417.51
  • JBJ-09-063 hydrochloride


    JBJ-09-063 hydrochloride: targeted EGFR inhibitor, effective for various mutations and TKI-resistant lung cancer models.
    Formula:C31H30ClFN4O3S
    Colore e forma:Solid
    Peso molecolare:593.11
  • Tyrphostin AG 112

    CAS:
    Tyrphostin AG 112 is an inhibitor of EGFR phosphorylation.
    Formula:C13H8N4O
    Purezza:99.14%
    Colore e forma:Solid
    Peso molecolare:236.23
  • Gefitinib N-oxide

    CAS:
    Gefitinib is an EGFR tyrosine kinase inhibitor, with IC50 of 2-37 nM in NR6wtEGFR cells. Gefitinib N-oxide is the N-oxide derivative of Gefitinib.
    Formula:C22H24ClFN4O4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:462.9
  • Epertinib

    CAS:
    <p>Epertinib is a reversible and selective tyrosine kinase inhibitor of EGFR, HER2, and HER4 (IC50s: 1.48 nM, 7.15 nM, and 2.49 nM).</p>
    Formula:C30H27ClFN5O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:560.02
  • EGFR-IN-50

    CAS:
    EGFR-IN-50, a potent EGFR blocker, hinders L858R mutation; GI50: 8 nM for TEL-EGFR-L858R, 6.03 μM for T790M-L858R; curbs cancer cell growth.
    Formula:C24H26BrN3O4S2
    Colore e forma:Solid
    Peso molecolare:564.51
  • EGFR-IN-75


    EGFR-IN-75 inhibits EGFR WT/T790M; IC50s: 0.28/5.02 μM. It has anticancer and antioxidant effects.
    Formula:C10H6N6S2
    Colore e forma:Solid
    Peso molecolare:274.32
  • BPIQ-II (hydrochloride)

    CAS:
    BPIQ-II, a selective EGFR inhibitor with an IC50 of 8 pM, targets ATP sites and halts EGF signals inside cells.
    Formula:C15H11BrClN5
    Colore e forma:Solid
    Peso molecolare:376.64
  • PF-6422899

    CAS:
    PF-6422899 irreversibly inhibits EGFR kinase activity by binding covalently to active-site cysteine residues in the ATP binding pocket of EGFR.
    Formula:C20H14ClFN4O2
    Colore e forma:Solid
    Peso molecolare:396.8
  • NSC114126

    CAS:
    NSC114126 is a potent, oral EGFR-TK inhibitor with strong antiproliferative effects, promising for cancer research.
    Formula:C22H20O4
    Colore e forma:Solid
    Peso molecolare:348.39
  • MJ04

    CAS:
    MJ04 is a selective inhibitor of Janus Kinase 3 (JAK3) with an IC50 of 2.03 nM. It hinders T cell differentiation and suppresses pro-inflammatory cytokines in macrophages induced by Lipopolysaccharides. In mice, MJ04 exhibits favorable pharmacokinetic properties and promotes hair growth in a DHT-induced alopecia model in athymic mice, without notable toxicity (LD50>2 g/kg).
    Formula:C20H16FN5
    Colore e forma:Solid
    Peso molecolare:345.37
  • EGFR-IN-53

    CAS:
    EGFR-IN-53 (Compound 7) is a potent inhibitor of EGFR (IC50 = 8.264 μM) that exhibits cytotoxic activity against cancer cell lines [1].
    Formula:C14H13N3O2S
    Colore e forma:Solid
    Peso molecolare:287.34
  • Selatinib

    CAS:
    <p>Selatinib is an orally active and potent dual inhibitor of EGFR and ErbB2 with anticancer activity that inhibits the growth of NCI-N87 tumor cells.</p>
    Formula:C29H26ClFN4O3S
    Purezza:98.00%
    Colore e forma:Solid
    Peso molecolare:565.06
  • Mutated EGFR-IN-3

    CAS:
    Mutated EGFR-IN-3: ATP-competitive, selective dibenzodiazepinone inhibitor for EGFR mutations, IC50 12-13 nM.
    Formula:C31H29FN4O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:508.59
  • EGFR-IN-28

    CAS:
    EGFR-IN-28 is a potent EGFR inhibitor. EGFR-IN-28 has antitumor activity .
    Formula:C31H39BrN10O3S
    Colore e forma:Solid
    Peso molecolare:711.68
  • BAY 2476568

    CAS:
    BAY 2476568 is a selective and potent EGFR inhibitor that acts on both wild-type EGFR (IC50 <0.2 nM) and mutant EGFR (IC50 <0.2 nM).
    Formula:C24H27FN4O4
    Colore e forma:Solid
    Peso molecolare:454.49
  • JNJ28871063 hydrochloride

    CAS:
    ErbB receptor family inhibitor
    Formula:C24H28Cl2N6O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:519.42
  • EGFR-IN-64

    CAS:
    EGFR-IN-64 inhibits EGFR with 0.33 μM IC50, showing promising anticancer properties.
    Formula:C20H21N3O3
    Colore e forma:Solid
    Peso molecolare:351.4