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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 3888 productos de "Ciclo celular / Checkpoint"

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  • EFdA-TP tetraammonium


    EFdA-TP tetraammonium is a potent HIV-1 RT inhibitor and DNA synthesis blocker, acting as an ICT or DCT.
    Fórmula:C12H27N9O12P3
    Forma y color:Solid
    Peso molecular:601.31

    Ref: TM-T35649

    1mg
    432,00€
    5mg
    1.071,00€
  • Evybactin


    Evybactin: a selective DNA gyrase inhibitor for Mycobacterium tuberculosis (MIC 0.25 µg/mL), first of its kind.
    Fórmula:C64H89N21O21
    Forma y color:Solid
    Peso molecular:1488.52

    Ref: TM-T76266

    5mg
    A consultar
    50mg
    A consultar
  • DSPE-PEG2000-iRGD


    DSPE-PEG2000-iRGD is a PEG compound composed of DSPE and the αv-integrin targeting peptide (iRGD). The iRGD peptide binds to αv-integrins and subsequently undergoes proteolytic cleavage within tumors, producing CRGDK/R, which interacts with neuropilin-1. This compound is characterized by its tumor-targeting and tumor-penetrating properties, making DSPE-PEG2000-iRGD suitable for drug delivery applications.
    Forma y color:Odour Solid

    Ref: TM-TCL-01137

    10mg
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    50mg
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  • FF-10502

    CAS:
    FF-10502, a pyrimidine analog of Gemcitabine, inhibits DNA polymerases α/β, targeting dormant cancer cells.
    Fórmula:C9H12FN3O3S
    Forma y color:Solid
    Peso molecular:261.27

    Ref: TM-T39290

    25mg
    1.369,00€
  • 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
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    50mg
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  • 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€
  • RNA splicing modulator 1

    CAS:

    RNA Splicing Modulator 1 (Compound 233) is a modulator of RNA splicing, exhibiting an AC50 value of less than 100 nM [1].

    Fórmula:C19H20N6OS
    Forma y color:Solid
    Peso molecular:380.47

    Ref: TM-T74884

    5mg
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    50mg
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  • R-1479

    CAS:
    R-1479 (4'-Azidocytidine) is an RdRp inhibitor with an IC50 value of 1.28 μM for HCV RNA replication in the HCV subgenomic replicon system.
    Fórmula:C9H12N6O5
    Pureza:98.11% - 99.95%
    Forma y color:Solid
    Peso molecular:284.23

    Ref: TM-TQ0162

    1mg
    104,00€
    5mg
    258,00€
    10mg
    358,00€
    25mg
    595,00€
    50mg
    842,00€
    100mg
    1.134,00€
    200mg
    1.521,00€
    1mL*10mM (DMSO)
    318,00€
  • AD16

    CAS:
    AD16 (Acetamide) acts as an inhibitor of LINE-1 retrotransposon endonuclease, exhibiting an IC50 value of 4.7 μM. It decreases LINE-1 retrotransposition in senescent cells and mitigates the resulting DNA damage and inflammation.
    Fórmula:C24H20N14O3S2
    Forma y color:Solid
    Peso molecular:616.64

    Ref: TM-T88160

    25mg
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    50mg
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    100mg
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  • CBP501 Affinity Peptide

    CAS:
    CBP501 Affinity Peptide, a Chk kinase inhibitor, disrupts G2 arrest triggered by DNA-damaging agents and is utilized in cancer research [1].
    Fórmula:C68H119N21O25S
    Forma y color:Solid
    Peso molecular:1662.86

    Ref: TM-T80132

    5mg
    A consultar
    50mg
    A consultar
  • 5'-O-TBDMS-Bz-dA

    CAS:
    5’-O-TBDMS-Bz-dA is a nucleoside with protective and modification effects.
    Fórmula:C23H31N5O4Si
    Forma y color:Solid
    Peso molecular:469.617

    Ref: TM-T37142

    50mg
    47,00€
    1mL*10mM (DMSO)
    52,00€
  • Bimosiamose disodium

    CAS:
    Bimosiamose disodium (TBC-1269Z), a pan-selectin inhibitor, has IC50s: E-selectin 88 μM, P-selectin 20 μM, L-selectin 86 μM; anti-inflammatory.
    Fórmula:C46H52Na2O16
    Pureza:98%
    Forma y color:Solid
    Peso molecular:906.88

    Ref: TM-T14573

    25mg
    1.369,00€
  • RP-1664

    CAS:
    RP-1664,PLK4 inhibitor (IC50=3 nM). Disrupts centriole biogenesis. Antitumor activity in breast cancer, neuroblastoma.
    Fórmula:C23H24F2N8O2S
    Pureza:99.04%
    Forma y color:Soild
    Peso molecular:514.55

    Ref: TM-T206047

    1mg
    219,00€
    5mg
    530,00€
    10mg
    772,00€
    25mg
    1.153,00€
    50mg
    1.549,00€
  • dCeMM3 

    CAS:

    dCeMM3 is a glue degrader that induces ubiquitination and degradation of cyclin K by promoting CDK12-cyclin K interaction with CRL4B ligase.

    Fórmula:C14H11ClN4OS
    Pureza:98.48% - 99.41%
    Forma y color:Solid
    Peso molecular:318.78

    Ref: TM-T9758

    5mg
    51,00€
    10mg
    88,00€
    25mg
    160,00€
    50mg
    250,00€
    100mg
    406,00€
  • ROCK-IN-32

    CAS:
    ROCK-IN-32 is an effective Rho-kinase inhibitor.
    Fórmula:C20H17Cl2N3O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:402.27

    Ref: TM-T24722

    25mg
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    50mg
    A consultar
    100mg
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  • (S)-DI-87

    CAS:
    (S)-DI-87 is an isomer of DI-87, a oral dCK inhibitor,reduce dNTP production and cell cycle arrest. significantly inhibits tumor growth with thymidine.
    Fórmula:C23H30N6O3S2
    Pureza:99.42%
    Forma y color:Soild
    Peso molecular:502.65

    Ref: TM-T39550L

    1mg
    185,00€
    5mg
    459,00€
    10mg
    657,00€
    25mg
    1.026,00€
    50mg
    1.415,00€
    100mg
    1.872,00€
    200mg
    2.555,00€
  • 5'(R)-C-Methyl-5-fluorouridine


    5’(R)-C-Methyl-5-fluorouridine, a uridine analogue, possesses potential antiepileptic properties.
    Fórmula:C10H13FN2O6
    Forma y color:Solid
    Peso molecular:276.22

    Ref: TM-T75079

    5mg
    A consultar
    50mg
    A consultar
  • Aclacinomycin A

    CAS:
    Aclacinomycin A has a wide range of applications in life science related research.
    Fórmula:C42H53NO15
    Pureza:99.43%
    Forma y color:Solid
    Peso molecular:811.87

    Ref: TM-T21502

    1mg
    269,00€
  • CPS2

    CAS:
    CPS2: potent, selective PROTAC CDK2 degrader. IC50=24nM, targets acute myeloid leukemia research.
    Fórmula:C38H42N12O10S2
    Forma y color:Solid
    Peso molecular:890.94

    Ref: TM-T74181

    5mg
    623,00€
    10mg
    1.161,00€
  • BLINK15


    BLINK15 is a blood-brain barrier-permeable Cdk5 inhibitor. It reduces CDK5 activity in CDK5/p35 (IC50= 29.34 nM) and CDK5/p25 (IC50= 12.08 nM) complexes. Additionally, BLINK15 exhibits antidiabetic and neuroprotective effects. It lowers blood glucose levels in type 2 diabetes (T2D) mice, enhances cognitive abilities, and diminishes neurodegenerative lesions.
    Forma y color:Odour Solid

    Ref: TM-T206737

    10mg
    A consultar
    50mg
    A consultar