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Ciclo celular / Checkpoint

Ciclo celular / Checkpoint

Los inhibidores del ciclo celular/puntos de control son compuestos que interrumpen la progresión normal del ciclo celular, particularmente en puntos de control regulatorios clave. Estos inhibidores son cruciales para estudiar la división celular, comprender la proliferación de células cancerosas y desarrollar terapias anticancerígenas. Al dirigirse a fases específicas del ciclo celular, estos inhibidores pueden inducir la detención del ciclo celular, lo que lleva a apoptosis o senescencia en células de división rápida. En CymitQuimica, ofrecemos una amplia gama de inhibidores de alta calidad del ciclo celular/puntos de control para apoyar su investigación en biología del cáncer, biología celular y desarrollo de fármacos.

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Se han encontrado 3905 productos de "Ciclo celular / Checkpoint"

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  • DHODH-IN-16

    CAS:
    DHODH-IN-16 is an effective inhibitor of dihydroorotate dehydrogenase (DHODH, IC50 = 0.396 nM for human).
    Fórmula:C24H25FN4O3
    Pureza:99.64%
    Forma y color:Solid
    Peso molecular:436.48

    Ref: TM-T40168

    1mg
    72,00€
    5mg
    160,00€
    10mg
    A consultar
    25mg
    A consultar
    50mg
    A consultar
    1mL*10mM (DMSO)
    170,00€
  • PROTAC CDK9 degrader-2

    CAS:
    PROTAC CDK9 degrader-2, potent, selective, IC50 17 μM in MCF-7, wogonin-derived, targets CRBN.
    Fórmula:C39H36N6O10
    Pureza:98%
    Forma y color:Solid
    Peso molecular:748.74

    Ref: TM-T17728

    100mg
    A consultar
    500mg
    A consultar
  • CDK8-IN-12

    CAS:
    CDK8-IN-12: selective CDK8 inhibitor (Ki 14 nM), oral anticancer, blocks GSK-3α/β, PCK-θ, halts MV4-11 cell growth.
    Fórmula:C21H20ClN3O2
    Pureza:98.55% - 99.22%
    Forma y color:Soild
    Peso molecular:381.86

    Ref: TM-T72048

    1mg
    52,00€
    5mg
    101,00€
    10mg
    150,00€
    25mg
    250,00€
    50mg
    363,00€
    100mg
    509,00€
    200mg
    695,00€
    1mL*10mM (DMSO)
    116,00€
  • 5'-O-TBDMS-N2-ibu-dG

    CAS:
    5'-O-TBDMS-N2-ibu-dG: a nucleoside derivative with strong anti-BVDV activity, useful in lead compound synthesis.
    Fórmula:C20H33N5O5Si
    Forma y color:Solid
    Peso molecular:451.59

    Ref: TM-T40949

    100mg
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    500mg
    A consultar
  • CDK7-IN-5

    CAS:
    CDK7-IN-5, a CDK7 inhibitor with an IC 50 value of less than 100 nM, exhibits potent anticancer properties (WO2015154022A1, Compound 104).
    Fórmula:C34H45N9O2
    Forma y color:Solid
    Peso molecular:611.795

    Ref: TM-T39247

    5mg
    873,00€
  • EC0489

    CAS:
    EC0489, Small molecule-drug conjugate (SMDC) ,a conjugate of folic acid and desacetyl vinblastine hydrazide, is a high-affinity ligand for the folate receptor (
    Fórmula:C111H156N22O43S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2550.7

    Ref: TM-T13672

    25mg
    A consultar
  • 5'-O-DMT-N2-DMF-dG

    CAS:
    5'-O-DMT-2'-O-TBDMS-rI, a modified nucleoside, finds application in deoxyribonucleic acid (DNA) or nucleic acid synthesis.
    Fórmula:C34H36N6O6
    Forma y color:Solid
    Peso molecular:624.698

    Ref: TM-T40500

    100mg
    A consultar
    500mg
    A consultar
  • DG1


    DG1 (Compound 8Nc), a Thymidylate Synthase (TS) inhibitor, impedes angiogenesis and alters metabolic reprogramming in NSCLC cells, while effectively suppressing
    Fórmula:C19H17N5O5S
    Forma y color:Solid
    Peso molecular:427.43

    Ref: TM-T78751

    5mg
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    50mg
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  • Antibacterial agent 144


    Antibacterial Agent 144 (compound 8e) exhibits superior efficacy against multi-resistant Staphylococcus aureus compared to Chloromycin and Amoxicillin.
    Fórmula:C26H23N7O3
    Forma y color:Solid
    Peso molecular:481.51

    Ref: TM-T79282

    5mg
    A consultar
    50mg
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  • 3,6-DMAD hydrochloride


    3,6-DMAD hydrochloride functions as an inhibitor for the IRE1α-XBP1 pathway within the unfolded protein response mechanism.
    Fórmula:C22H31N5xHCl
    Pureza:98%
    Forma y color:Solid
    Peso molecular:365.52

    Ref: TM-T10102

    25mg
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    50mg
    A consultar
    100mg
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  • TTK/PLK1-IN-1

    CAS:
    TTK/PLK1-IN-1 (Formula I) is a dual inhibitor of TTK (threonine tyrosine kinase) and PLK1 (polo-like kinase 1), with IC₅₀ values of 7 nM and 72 nM respectively.
    Fórmula:C30H33N7O2
    Pureza:97.39%
    Forma y color:Solid
    Peso molecular:523.63

    Ref: TM-T203064

    1mg
    379,00€
    5mg
    872,00€
    10mg
    1.153,00€
    25mg
    1.738,00€
    50mg
    2.332,00€
  • STX-100


    PY314 is a CHO-expressed humanized monoclonal antibody targeting TREM2 with antitumor activity for the study of metastatic renal cell carcinoma.
    Pureza:97.3% (SDS-PAGE); 97.5% (SEC-HPLC) - 97.3% (SDS-PAGE); 97.5% (SEC-HPLC)
    Forma y color:Odour Liquid
    Peso molecular:145.12 kDa

    Ref: TM-T9901A-062

    1mg
    233,00€
    5mg
    754,00€
    10mg
    1.228,00€
    25mg
    2.257,00€
    50mg
    3.046,00€
  • 5'-O-TBDMS-dG

    CAS:
    5’-O-TBDMS-dG is a modified nucleoside. 5’-O-DMT-2’-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid.
    Fórmula:C16H27N5O4Si
    Forma y color:Solid
    Peso molecular:381.50

    Ref: TM-T37144

    50mg
    47,00€
    1mL*10mM (DMSO)
    52,00€
  • TMX-2138

    CAS:
    TMX-2138 is a CDKs PROTAC degrader, with IC50 values of 8.7 nM for CDK1/cyclinB, 10.9 nM for CDK2/cyclinA, 7.0 nM for CDK5/p25, and 25.7 nM for CDK9/cyclinT1. It enhances the ubiquitination and degradation of CDKs and is utilized for ovarian cancer research.
    Fórmula:C40H43BrFN9O11S
    Forma y color:Solid
    Peso molecular:956.791

    Ref: TM-T204343

    10mg
    A consultar
    50mg
    A consultar
  • CD532 hydrochloride


    CD532 hydrochloride, potent Aurora A inhibitor (IC50=45 nM), hampers MYCN protein, changes AURKA's shape, aids cancer research.
    Forma y color:Solid

    Ref: TM-T36932

    5mg
    90,00€
    10mg
    155,00€
    25mg
    291,00€
  • KIF2C-IN-1


    KIF2C-IN-1 (Compound 7S9) is a selective and potent small molecule inhibitor of KIF2C. It stabilizes the interaction between KIF2C and microtubule proteins, preventing the depolymerization of polyglutamylated microtubules. KIF2C-IN-1 enhances the cytotoxicity of Paclitaxel in Paclitaxel-resistant triple-negative breast cancer (TNBC) cells and, when combined with Paclitaxel, significantly reduces tumor growth in mouse models.
    Fórmula:C36H39ClN4O9S
    Forma y color:Solid
    Peso molecular:738.21263

    Ref: TM-T207280

    10mg
    A consultar
    50mg
    A consultar
  • Chrexanthomycin C


    Chrexanthomycin C, orally active, binds DNA (G4C2)4 G4, Kd 2.8 mM, potential in ALS research.
    Fórmula:C31H24O15
    Forma y color:Solid
    Peso molecular:636.51

    Ref: TM-T75527

    5mg
    A consultar
    50mg
    A consultar
  • N7-Methyl-guanosine-5'-triphosphate-5'-adenosine diammonium

    CAS:

    N7-Methylguanosine-5'-triphosphate-5'-adenosine (m7GpppA) diammonium, a dinucleotide cap analog, facilitates in vitro RNA transcription [1].

    Fórmula:C21H35N12O17P3
    Forma y color:Solid
    Peso molecular:820.49

    Ref: TM-T74135

    5mg
    A consultar
    50mg
    A consultar
  • [pSer2, pSer5, pSer7]-CTD TFA


    Substrate '[pSer2, pSer5, pSer7]-CTD (TFA)' for CDK7 phosphorylates RNA Pol II CTD at ser2, 5, 7.
    Fórmula:C98H138F3N21O39
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2291.25

    Ref: TM-TP1641

    100mg
    A consultar
    500mg
    A consultar
  • 11H-Benzo[a]carbazole

    CAS:
    11H-Benzo[a]carbazole is a kinesin-like protein KIF11 inhibitor that can inhibit the viability of HeLa cells.
    Fórmula:C16H11N
    Pureza:99.14%
    Forma y color:Solid
    Peso molecular:217.27

    Ref: TM-TN9686

    50mg
    39,00€
    100mg
    52,00€