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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 3827 productos de "Ciclo celular / Checkpoint"

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  • Antitumor agent-75


    Antitumor agent-75 is a novel and potent antitumor agent.
    Fórmula:C26H23FN6
    Forma y color:Solid
    Peso molecular:438.5

    Ref: TM-T62510

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Zorubicin

    CAS:
    Zorubicin, a Daunorubicin derivative, targets topoisomerase II, inhibits DNA polymerase, and researches acute leukemia, sarcomas.
    Fórmula:C34H35N3O10
    Forma y color:Solid
    Peso molecular:645.66

    Ref: TM-T69130

    25mg
    4.069,00€
    50mg
    5.383,00€
    100mg
    7.650,00€
  • RAD51-IN-5

    CAS:
    RAD51-IN-5 blocks RAD51; may aid mitochondrial disorder research. (WO2021164746A1, cmpd 3)
    Fórmula:C26H38N4O5S2
    Forma y color:Solid
    Peso molecular:550.73

    Ref: TM-T63892

    25mg
    1.791,00€
    50mg
    2.872,00€
  • Dyrk1A-IN-8

    CAS:
    Dyrk1A-IN-8 is an active molecule that can be used in life science related research. The CAS number of Dyrk1A-IN-8 is 101578-13-6.
    Fórmula:C17H21N3O
    Forma y color:Solid
    Peso molecular:283.37

    Ref: TM-T87614

    10mg
    A consultar
    50mg
    A consultar
  • WEE1/PKMYT1-IN-1

    CAS:

    WEE1/PKMYT1-IN-1 (compound 75) is an effective and orally bioavailable inhibitor of WEE1 and PKMYT1. It demonstrates antiproliferative activity.

    Fórmula:C16H16N4O3
    Forma y color:Solid
    Peso molecular:312.323

    Ref: TM-T204368

    10mg
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    50mg
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  • MKLP2-IN-1

    CAS:
    MKLP2-IN-1 (compound 12a) is an inhibitor of MKLP2 that demonstrates excellent oral bioactivity. In vitro, MKLP2-IN-1 inhibits the ATPase activity stimulated by recombinant MKLP2 microtubules and, in a mouse Calu-6 lung cancer model, it effectively suppresses tumor growth.
    Fórmula:C23H19BrFN3O2
    Forma y color:Solid
    Peso molecular:468.318

    Ref: TM-T205538

    10mg
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    50mg
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  • PCNA-IN-1

    CAS:
    PCNA-IN-1 (Compound 11) is an inhibitor of the PCNA/PIP-box interaction, with an IC50 greater than 50 μM. It is applicable in cancer research.
    Fórmula:C19H18I3NO3
    Forma y color:Solid
    Peso molecular:689.065

    Ref: TM-T204170

    10mg
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    50mg
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  • CDK2-IN-39

    CAS:
    CDK2-IN-39 (compound 4) is a CDK2 inhibitor.
    Fórmula:C14H15N3O4S
    Forma y color:Solid
    Peso molecular:321.352

    Ref: TM-T204890

    10mg
    A consultar
    50mg
    A consultar
  • CDK2-IN-40

    CAS:
    CDK9-IN-40 is an inhibitor of CDK2 (Cyclin-dependent kinase 2). It effectively inhibits CDK2/Cyclin E1, with an IC50 of ≤ 10 nM.
    Fórmula:C16H21N7O2
    Forma y color:Solid
    Peso molecular:343.384

    Ref: TM-T205452

    10mg
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    50mg
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  • MU147

    CAS:
    MU147 is an MRE11 nuclease inhibitor and chemical probe with anticancer properties, exhibiting lethal effects on Ehrlich ascites tumor cells both in vivo and in vitro. It disrupts the MRE11 nuclease-dependent double-strand break repair mechanism without impairing ATM activation. Additionally, MU147 damages the degradation of nascent strands at stalled replication forks and selectively affects BRCA2-deficient cells.
    Fórmula:C19H13N3O3S
    Forma y color:Solid
    Peso molecular:363.39

    Ref: TM-T205293

    10mg
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    50mg
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  • 2-CEES

    CAS:
    2-CEES is a mustard gas analogue that only forms DNA monoadducts. It induces centromere amplification in both human and mouse cells and can lead to chromosome instability.
    Fórmula:C4H9ClS
    Forma y color:Solid
    Peso molecular:124.632

    Ref: TM-T204286

    10mg
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    50mg
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  • TREX1-IN-3

    CAS:
    TREX1-IN-3 (Compound 95) is an inhibitor of TREX1 and TREX2, with an IC50 of less than 0.1 μM for TREX1 and less than 1 μM for TREX2, as well as an EC50 of less than 1 μM for HCT116 cells. It is applicable for research in the field of cancer.
    Fórmula:C24H19ClN6O4
    Forma y color:Solid
    Peso molecular:490.898

    Ref: TM-T205254

    10mg
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    50mg
    A consultar
  • DDO-6079

    CAS:
    DDO-6079 is an efficient CDC37 inhibitor. It suppresses the HSP90-CDC37 and CDC37-CDK4/6 chaperone complexes by binding to an allosteric site on CDC37. Additionally, DDO-6079 reduces the thermal stability of CDK6.
    Fórmula:C18H13ClN2O3
    Forma y color:Solid
    Peso molecular:340.76

    Ref: TM-T204112

    10mg
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    50mg
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  • GSK3335103

    CAS:
    GSK3335103 is a non-peptide, orally active inhibitor of αvβ6 integrin (pIC50=8), employed in the study of pulmonary fibrosis.
    Fórmula:C27H36FN3O4
    Forma y color:Solid
    Peso molecular:485.59

    Ref: TM-T200463

    25mg
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    50mg
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    100mg
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  • PLK1-IN-5

    CAS:
    PLK1-IN-5, a potent PLK1 inhibitor, has an IC50 of less than 500 nM and demonstrates anticancer effects (WO2008113711A1; compound I-4) [1].
    Fórmula:C28H39N7O3
    Forma y color:Solid
    Peso molecular:521.65

    Ref: TM-T87222

    10mg
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    50mg
    A consultar
  • MtTMPK-IN-5


    MtTMPK-IN-5 inhibits Mtb TMPK with IC50 of 34 μM and fights tuberculosis with MIC of 12.5 μM, aiding TB research.
    Fórmula:C21H23N5O2
    Forma y color:Solid
    Peso molecular:377.44

    Ref: TM-T61573

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • Z4P

    CAS:
    Z4P, an IRE1 inhibitor with blood-brain barrier permeability (BBB), inhibited glioblastoma growth and recurrence in combination with Temozolomide.
    Fórmula:C19H24N2O2
    Pureza:98.99%
    Forma y color:Solid
    Peso molecular:312.41

    Ref: TM-T87658

    1mg
    77,00€
    5mg
    167,00€
    10mg
    268,00€
    25mg
    537,00€
    50mg
    858,00€
    100mg
    1.333,00€
    200mg
    1.783,00€
    1mL*10mM (DMSO)
    178,00€
  • WEE1-IN-10

    CAS:
    WEE1-IN-10 is a Wee1 kinase inhibitor that inhibits the growth of LOVO cells, such as pancreatic cancer, malignant melanoma, and malignant glioma.
    Fórmula:C28H30Cl2N8O
    Pureza:98.18%
    Forma y color:Solid
    Peso molecular:565.5

    Ref: TM-T89365

    1mg
    82,00€
    5mg
    215,00€
    10mg
    303,00€
    25mg
    518,00€
    50mg
    778,00€
  • NSC 641396

    CAS:
    NSC 641396 is a ribonucleotide reductase (RNR) inhibitor with an IC50 value of 1.2 μM. Additionally, it acts as an inhibitor of protein arginine N-methyltransferase 9 (PRMT9) and exhibits antitumor properties.
    Fórmula:C18H13NO3
    Forma y color:Solid
    Peso molecular:291.301

    Ref: TM-T204449

    10mg
    A consultar
    50mg
    A consultar
  • Elacytarabine

    CAS:
    Elacytarabine (M7594 0037), a lipid-conjugated derivative of the nucleoside analog cytarabine, is an antineoplastic drug. It has cytotoxicity in solid tumors.
    Fórmula:C27H45N3O6
    Pureza:97.69%
    Forma y color:Solid
    Peso molecular:507.66

    Ref: TM-T15009

    5mg
    35,00€
    10mg
    47,00€
    25mg
    66,00€
    50mg
    A consultar
    1mL*10mM (DMSO)
    35,00€