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Cell Cycle/Checkpoint

Cell Cycle/Checkpoint

Cell cycle/checkpoint inhibitors are compounds that disrupt the normal progression of the cell cycle, particularly at key regulatory checkpoints. These inhibitors are crucial for studying cell division, understanding cancer cell proliferation, and developing anti-cancer therapies. By targeting specific phases of the cell cycle, these inhibitors can induce cell cycle arrest, leading to apoptosis or senescence in rapidly dividing cells. At CymitQuimica, we offer a diverse range of high-quality cell cycle/checkpoint inhibitors to support your research in cancer biology, cell biology, and drug development.

Subcategories of "Cell Cycle/Checkpoint"

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Found 3934 products of "Cell Cycle/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).
    Formula:C24H25FN4O3
    Purity:99.64%
    Color and Shape:Solid
    Molecular weight:436.48

    Ref: TM-T40168

    10mg
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    25mg
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    50mg
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    1mg
    72.00€
    5mg
    160.00€
    1mL*10mM (DMSO)
    170.00€
  • Cy5-dATP


    Cy5-dATP is a Cy5 -labeled dATP . Cy5-dATP can be incorporated into a DNA primer [1] [2] .

    Formula:C47H58N7O19P3S2
    Color and Shape:Solid
    Molecular weight:1182.05

    Ref: TM-T75384

    5mg
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    50mg
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  • 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.
    Formula:C16H27N5O4Si
    Color and Shape:Solid
    Molecular weight:381.50

    Ref: TM-T37144

    50mg
    47.00€
    1mL*10mM (DMSO)
    52.00€
  • PROTAC CDK9 degrader-2

    CAS:
    PROTAC CDK9 degrader-2, potent, selective, IC50 17 μM in MCF-7, wogonin-derived, targets CRBN.
    Formula:C39H36N6O10
    Purity:98%
    Color and Shape:Solid
    Molecular weight:748.74

    Ref: TM-T17728

    100mg
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    500mg
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  • 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.
    Formula:C40H43BrFN9O11S
    Color and Shape:Solid
    Molecular weight:956.791

    Ref: TM-T204343

    10mg
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    50mg
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  • AR-13324 analog mesylate


    AR-13324 analog mesylate is an inhibitor of Rho-kinase and a norepinephrine transporter and reduces intraocular pressure in normotensive monkey eyes.
    Formula:C29H33N3O9S2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:631.72

    Ref: TM-T10357

    25mg
    2,673.00€
    50mg
    3,312.00€
    100mg
    4,230.00€
  • 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).
    Formula:C34H45N9O2
    Color and Shape:Solid
    Molecular weight:611.795

    Ref: TM-T39247

    5mg
    873.00€
  • DG1


    DG1 (Compound 8Nc), a Thymidylate Synthase (TS) inhibitor, impedes angiogenesis and alters metabolic reprogramming in NSCLC cells, while effectively suppressing
    Formula:C19H17N5O5S
    Color and Shape:Solid
    Molecular weight:427.43

    Ref: TM-T78751

    5mg
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    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.
    Formula:C22H31N5xHCl
    Purity:98%
    Color and Shape:Solid
    Molecular weight:365.52

    Ref: TM-T10102

    25mg
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    50mg
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    100mg
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  • Methylcarbamyl PAF C-8


    Methylcarbamyl PAF C-8 is resistant to degradation by PAF-AH and has a half-life of over 100 minutes in platelet-poor plasma, exhibiting platelet aggregation activity. In NRK-49 cells overexpressing PAF receptor, it induces the expression of c-myc, c-fos, and activates mitogen-activated protein kinase (MAPK). Furthermore, Methylcarbamyl PAF C-8 can induce G1 phase cell cycle arrest. This compound shows potential for research in cardiovascular and anti-cancer applications.
    Color and Shape:Odour Solid

    Ref: TM-T206879

    10mg
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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.
    Formula:C26H23N7O3
    Color and Shape:Solid
    Molecular weight:481.51

    Ref: TM-T79282

    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.
    Purity:97.3% (SDS-PAGE); 97.5% (SEC-HPLC) - 97.3% (SDS-PAGE); 97.5% (SEC-HPLC)
    Color and Shape:Odour Liquid
    Molecular weight: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€
  • Tirandamycin A


    Tirandamycin A is a useful organic compound for research related to life sciences and the catalog number is T124996.
    Formula:C22H27NO7
    Color and Shape:Solid
    Molecular weight:417.458

    Ref: TM-T124996

    1mg
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    5mg
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  • Cdk2/Cyclin Inhibitory Peptide I


    CDK2, a Ser/Thr kinase, is akin to yeast cdc28 and human Cdk1, crucial for cell division.
    Formula:C111H196N48O23
    Purity:98%
    Color and Shape:Solid
    Molecular weight:2571.05

    Ref: TM-TP2192

    5mg
    107.00€
    10mg
    170.00€
    25mg
    236.00€
  • CD532 hydrochloride


    CD532 hydrochloride, potent Aurora A inhibitor (IC50=45 nM), hampers MYCN protein, changes AURKA's shape, aids cancer research.
    Color and Shape: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.
    Formula:C36H39ClN4O9S
    Color and Shape:Solid
    Molecular weight:738.21263

    Ref: TM-T207280

    10mg
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    50mg
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  • Chrexanthomycin C


    Chrexanthomycin C, orally active, binds DNA (G4C2)4 G4, Kd 2.8 mM, potential in ALS research.
    Formula:C31H24O15
    Color and Shape:Solid
    Molecular weight:636.51

    Ref: TM-T75527

    5mg
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    50mg
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  • 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].

    Formula:C21H35N12O17P3
    Color and Shape:Solid
    Molecular weight:820.49

    Ref: TM-T74135

    5mg
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    50mg
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  • 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.
    Formula:C20H33N5O5Si
    Color and Shape:Solid
    Molecular weight:451.59

    Ref: TM-T40949

    100mg
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    500mg
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  • 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 (
    Formula:C111H156N22O43S2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:2550.7

    Ref: TM-T13672

    25mg
    To inquire