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Bcr-Abl

Bcr-Abl

Los inhibidores de Bcr-Abl son terapias dirigidas que inhiben la proteína de fusión Bcr-Abl, formada debido a la translocación del cromosoma Filadelfia y que es un impulsor de la leucemia mieloide crónica (LMC). Esta proteína también influye en la angiogénesis, contribuyendo a la progresión tumoral. Los inhibidores de Bcr-Abl son cruciales en el tratamiento de la LMC y se están explorando por su potencial para inhibir la angiogénesis en varios tipos de cáncer. En CymitQuimica, ofrecemos inhibidores de Bcr-Abl de alta calidad para apoyar su investigación en biología del cáncer, angiogénesis y terapias dirigidas.

Se han encontrado 129 productos para "Bcr-Abl".

productos por página.
  • Tyrosine kinase-IN-8


    Tyrosine kinase-IN-8 (compound 4e) is a BCR‐ABL1 tyrosine kinase inhibitor (TKI) exhibiting antiproliferative activity against the chronic myeloid leukemia (CML) cell line K562, with a CC50 of 0.8 µM. Tyrosine kinase-IN-8 is applicable for research in chronic leukemia.
    Fórmula:C31H21F2N7O2
    Forma y color:Solid
    Peso molecular:561.17248
  • SIAIS178

    CAS:
    SIAIS178 is a potent and selective degrader of BCR-ABL based on PROTAC technology (IC50 of 24 nM).
    Fórmula:C50H62ClN11O6S2
    Pureza:98.07%
    Forma y color:Solid
    Peso molecular:1012.68
  • P19As

    CAS:
    P19As is a BCR-ABL PROTAC degrader based on Asciminib, with a DC50 of approximately 200 nM for the wild-type BCR-ABL protein. It is capable of degrading the T315I mutant and demonstrates strong antiproliferative activity in BaF3-BCR-ABL (T315I) cells. P19As is applicable for research in chronic myeloid leukemia and acute lymphoblastic leukemia.
    Fórmula:C47H51ClF2N12O10
    Peso molecular:1017.45
  • SNIPER(ABL)-049


    SNIPER(ABL)-049, a compound that conjugates Imatinib (ABL inhibitor) with Bestatin (IAP ligand) through a linker, effectively reduces BCR-ABL protein levels,
    Fórmula:C52H66N10O8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:959.14
  • PROTAC BCR-ABL1 ligand 1

    CAS:
    GMB-475 is a PROTAC ligand targeting BCR-ABL1 for degradation via E3 ligase recruitment.
    Fórmula:C17H12F3N3O2
    Forma y color:Solid
    Peso molecular:347.29
  • SNIPER(ABL)-047


    SNIPER(ABL)-047, a compound that links HG-7-85-01 (an ABL inhibitor) to MV-1 (an IAP ligand) via a linker, effectively decreases the BCR-ABL protein levels,
    Fórmula:C67H82F3N11O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1274.5
  • SNIPER(ABL)-058

    CAS:
    SNIPER(ABL)-058, a compound that links Imatinib (ABL inhibitor) with a derivative of LCL161 (IAP ligand) through a linker, effectively decreases BCR-ABL protein
    Fórmula:C62H75N11O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1150.39
  • SNIPER(ABL)-020


    SNIPER(ABL)-020, a Dasatinib-Bestatin conjugate via linker, inhibits ABL and targets IAP, reducing BCR-ABL protein.
    Fórmula:C44H59ClN10O8S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:923.52
  • SNIPER(ABL)-019


    SNIPER(ABL)-019, a compound that links Dasatinib (ABL inhibitor) to MV-1 (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels, exhibiting a
    Fórmula:C60H77ClN12O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1177.85
  • Kinase Inhibitor Library


    A unique collection of xnum kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;
    Forma y color:Odour Solid
  • SNIPER(ABL)-024

    CAS:
    SNIPER(ABL)-024, a compound that conjugates GNF5 (ABL inhibitor) to an LCL161 derivative (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels,
    Fórmula:C52H61F3N8O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1031.15
  • SNIPER(ABL)-015


    SNIPER(ABL)-015, a compound that conjugates GNF5 (ABL inhibitor) to MV-1 (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels with a DC50 of 5
    Fórmula:C58H70F3N9O9
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1094.23
  • SNIPER(ABL)-013


    SNIPER(ABL)-013, a compound that links GNF5 (ABL inhibitor) with Bestatin (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels with a DC50 of
    Fórmula:C42H52F3N7O8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:839.9
  • Abl Cytosolic Substrate

    CAS:
    Abl Cytosolic Substrate is a substrate for Abelson tyrosine kinase (Abl ).
    Fórmula:C64H101N15O16
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1336.58
  • SNIPER(ABL)-050


    SNIPER(ABL)-050 is a chemical compound that combines Imatinib, an ABL inhibitor, with MV-1, an IAP ligand, using a linker.
    Fórmula:C68H84N12O9
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1213.47
  • SNIPER(ABL)-039

    CAS:
    SNIPER(ABL)-039, conjugating Dasatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of
    Fórmula:C54H68ClN11O9S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1114.77
  • FGFRs-IN-1


    FGFRs-IN-1 (Compound A16) is an orally active inhibitor targeting FGFR1/2/3/4, with IC50 values of 2.3, 7, 11, and 163 nM respectively. It also inhibits VEGFR1/2/3, Abl, and Flt3, with IC50 values of 61, 176, 112, 26, and 353 nM. The compound shows weak inhibition of CYP enzymes. FGFRs-IN-1 reduces the expression of α-SMA and collagen I, and it inhibits epithelial-mesenchymal transition (EMT) in A549 cells stimulated by TGF-β1. Additionally, FGFRs-IN-1 demonstrates anti-inflammatory activity in mouse models of lung fibrosis induced by Bleomycin and liver fibrosis induced by CCl4.
    Fórmula:C28H26Cl2N4O3
    Forma y color:Solid
    Peso molecular:537.44
  • PROTAC BCR-ABL Degrader-1


    PROTAC BCR-ABL Degrader-1 (compound PROTAC 1), featuring a 2-oxoethyl linker, promotes Bcr-Abl degradation through the ubiquitin-proteasome pathway and
    Fórmula:C43H40N10O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:792.84
  • SNIPER(ABL)-033

    CAS:
    SNIPER(ABL)-033, a compound that conjugates HG-7-85-01 (ABL inhibitor) to a LCL161 derivative (IAP ligand) via a linker, effectively reduces BCR-ABL protein
    Fórmula:C61H73F3N10O9S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1211.42
  • Tyrosine Kinase Inhibitor Library


    A unique collection of xnum HIF-1 related small chemicals can be used for drug discovery in ischemic disease and cancer and related mechanism studies;
    Forma y color:Odour Solid