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ALK

ALK

Gli inibitori di ALK sono composti che mirano specificamente e inibiscono la chinasi del linfoma anaplastico (ALK), una tirosina chinasi recettoriale coinvolta nello sviluppo e nella progressione di alcuni tipi di cancro, inclusi il carcinoma polmonare non a piccole cellule e il neuroblastoma. Inibendo ALK, questi composti bloccano le vie di segnalazione che promuovono la crescita e la sopravvivenza delle cellule tumorali. Presso CymitQuimica, offriamo inibitori di ALK per supportare la tua ricerca in oncologia, terapie mirate contro il cancro e trasduzione del segnale.

Trovati 124 prodotti di "ALK"

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  • A 83-01

    CAS:
    A 83-01 (ALK5 Inhibitor IV) is a selective inhibitor of TGF-β type I receptor ALK5 kinase, type I activin/nodal receptor ALK4 and type I nodal receptor ALK7.
    Formula:C25H19N5S
    Purezza:97% - 98.2%
    Colore e forma:Solid
    Peso molecolare:421.52
  • Crizotinib

    CAS:
    Crizotinib (PF-02341066) is an ATP-competitive small-molecule tyrosine kinases inhibitor of c-MET (IC50: 8 nM) and ALK (IC50: 20 nM) receptor.
    Formula:C21H22Cl2FN5O
    Purezza:99% - 99.87%
    Colore e forma:Solid
    Peso molecolare:450.34
  • BIBF0775

    CAS:
    <p>BIBF0775 is a selective TGFβ type I receptor (Alk5) inhibitor (IC50: 34 nM).</p>
    Formula:C31H34N4O2
    Purezza:99.45% - 99.79%
    Colore e forma:Solid
    Peso molecolare:494.63
  • R-268712

    CAS:
    R-268712 is a potent ALK5 inhibitor with a 2.5 nM IC50, also targeting TGF-β type I receptor orally.
    Formula:C20H18FN5O
    Purezza:99.61%
    Colore e forma:Solid
    Peso molecolare:363.39
  • CH5424802 analog

    CAS:
    CH5424802 analog is a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant.
    Formula:C28H30N4O2
    Purezza:98.96%
    Colore e forma:Solid
    Peso molecolare:454.56
  • Lorlatinib

    CAS:
    Lorlatinib (PF-6463922) is an orally available, ATP-competitive inhibitor of the receptor tyrosine kinases, anaplastic lymphoma kinase (ALK) and C-ros oncogene
    Formula:C21H19FN6O2
    Purezza:99.77% - 99.95%
    Colore e forma:Solid
    Peso molecolare:406.41
  • Ensartinib

    CAS:
    Ensartinib (X-396) is a potent and orally active dual ALK/MET inhibitor for the treatment of ALK-positive non-small cell lung cancer (NSCLC).
    Formula:C26H27Cl2FN6O3
    Purezza:99.92%
    Colore e forma:Solid
    Peso molecolare:561.44
  • DMH-1

    CAS:
    <p>DMH-1 is a BMP inhibitor that inhibits ALK1, ALK2, ALK3 and ALK6. DMH-1 promotes pluripotent stem cell differentiation. Cost-effective and quality-assured.</p>
    Formula:C24H20N4O
    Purezza:98% - 99.92%
    Colore e forma:Solid
    Peso molecolare:380.44
  • Blu-782

    CAS:
    <p>Blu-782 (ALK2-IN-1) is a activin receptor-like kinase-2 (ALK2) inhibitor ( IC50 of &lt;10 nM)</p>
    Formula:C31H42N6O4
    Purezza:99.51%
    Colore e forma:Solid
    Peso molecolare:562.7
  • LDN-212854

    CAS:
    LDN-212854 (BMP Inhibitor III), a novel BMP inhibitor, exhibits greater selectivity for BMP versus the TGF-β type I receptors.
    Formula:C25H22N6
    Purezza:98% - 98.71%
    Colore e forma:Solid
    Peso molecolare:406.48
  • Alectinib hydrochloride

    CAS:
    <p>Alectinib hydrochloride (RO5424802 Hydrochloride) is a selective, and orally available inhibitor of ALK( IC50 : 1.9 nM)</p>
    Formula:C30H35ClN4O2
    Purezza:99.61% - 99.96%
    Colore e forma:Solid
    Peso molecolare:519.08
  • N-((4-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-5-(6-methylpyridin-2-yl)-1H-imidazol-2-yl)methyl)-2-bromoaniline

    CAS:
    Compound 12d is a potent ALK5 inhibitor with an IC50 of 7nM.
    Formula:C22H18BrN7
    Purezza:99.935%
    Colore e forma:Solid
    Peso molecolare:460.33
  • ALK kinase inhibitor-1

    CAS:
    SAR348830 is an ALK inhibitor, targeting anaplastic lymphoma kinase.
    Formula:C28H32FN5O3S
    Purezza:99.84%
    Colore e forma:Solid
    Peso molecolare:537.65
  • A 83-01 sodium salt

    CAS:
    A 83-01 sodium salt inhibits ALK5, ALK4, and ALK7 kinases with IC50s: 12, 45, 7.5 nM.
    Formula:C25H19N5NaS
    Colore e forma:Solid
    Peso molecolare:444.51
  • SB-505124 hydrochloride

    CAS:
    SB-505124 hydrochloride (SB505124 hydrochloride) is a TGF-β type I receptor (ALK4, ALK5, ALK7) inhibitor for the study of colorectal cancer.
    Formula:C20H22ClN3O2
    Purezza:98.71%
    Colore e forma:Solid
    Peso molecolare:371.86
  • AZ 12799734

    CAS:
    AZ 12799734 is an orally active, selective and potent dual inhibitor of TGFBR1 and ALK5 with inhibitory effects on BMP and TGFβ for the study of tumours.
    Formula:C18H18N4O3S
    Purezza:98.23%
    Colore e forma:Solid
    Peso molecolare:370.43
  • ALK5-IN-79

    CAS:
    ALK5-IN-79 (compound 57), an ALK inhibitor, exhibits anticancer activity by inhibiting the TGF-β1/SMAD signaling pathway. It effectively reduces the production of extracellular matrix (ECM) and collagen deposition. Moreover, ALK5-IN-79 demonstrates satisfactory pharmacokinetic (PK) properties and favorable in vivo tolerance.
    Formula:C23H27N7O
    Colore e forma:Solid
    Peso molecolare:417.51
  • ALK5-IN-26

    CAS:
    ALK5-IN-26 (EX-22) is an ALK (Activin receptor-like kinase) inhibitor. ALK5-IN-26 inhibits ALK5 (IC50 ≤ 1 nM).
    Formula:C24H25FN8
    Colore e forma:Solid
    Peso molecolare:444.51
  • TGFBR1-IN-1

    CAS:
    TGFBR1-IN-1 is an inhibitor of ALK5 (IC50 of 10-100 nM).
    Formula:C23H17N5O2S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:427.48
  • ALK-IN-21

    CAS:
    ALK-IN-21 (B10) inhibits ALK WT (IC50: 4.59nM), L1196M (2.07nM), G1202R (5.95nM); curbs Karpas299, H2228 cell growth; for ALCL research.
    Formula:C35H45ClN6O6S4
    Colore e forma:Solid
    Peso molecolare:809.48