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Ciclo cellulare/Checkpoint

Ciclo cellulare/Checkpoint

Gli inibitori del ciclo cellulare/dei checkpoint sono composti che interrompono la normale progressione del ciclo cellulare, in particolare nei principali punti di controllo regolatori. Questi inibitori sono fondamentali per studiare la divisione cellulare, comprendere la proliferazione delle cellule cancerose e sviluppare terapie antitumorali. Mirando a fasi specifiche del ciclo cellulare, questi inibitori possono indurre l'arresto del ciclo cellulare, portando all'apoptosi o alla senescenza nelle cellule che si dividono rapidamente. Presso CymitQuimica, offriamo una vasta gamma di inibitori di alta qualità del ciclo cellulare/dei checkpoint per supportare le tue ricerche in biologia del cancro, biologia cellulare e sviluppo di farmaci.

Sottocategorie di "Ciclo cellulare/Checkpoint"

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Trovati 3749 prodotti di "Ciclo cellulare/Checkpoint"

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  • CDK12-IN-6

    CAS:
    CDK12-IN-6, a pyrazolotriazine, strongly inhibits CDK12 (IC50 1.19 μM at 2 mM ATP), but not CDK2/Cyclin E or CDK9/Cyclin T1 (both IC50 >20 μM).
    Formula:C20H21F2N9
    Colore e forma:Solid
    Peso molecolare:425.448
  • LY2812223

    CAS:
    LY2812223: selective mGlu2 agonist; binds mGlu2/mGlu3 (Ki=144/156 nM).
    Formula:C10H12N4O4S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:284.29
  • CCT241533 dihydrochloride

    CAS:
    Potent Chk2 inhibitor with 3 nM IC50, 63-fold more selective over Chk1, affects 84 kinases, reduces DNA damage response and apoptosis in cells.
    Formula:C23H29Cl2FN4O4
    Colore e forma:Solid
    Peso molecolare:515.41
  • Isocytosine

    CAS:
    Compound PDK0016, with CAS No. 108-53-2, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0016 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.
    Formula:C4H5N3O
    Colore e forma:White To Off-White Solid
    Peso molecolare:111.1
  • Antibacterial agent 144


    Antibacterial Agent 144 (compound 8e) exhibits superior efficacy against multi-resistant Staphylococcus aureus compared to Chloromycin and Amoxicillin.
    Formula:C26H23N7O3
    Colore e forma:Solid
    Peso molecolare:481.51
  • Flurocitabine HCl

    CAS:
    Fluorocitabine HCl, a cytarabine analog, hydrolyzes into ara-FC and ara-FU, showing antitumor effects in leukemia and solid cancers.
    Formula:C9H11ClFN3O4
    Purezza:99.23% - 99.76%
    Colore e forma:Soild
    Peso molecolare:279.65
  • 5'-ODMT cEt G Phosphoramidite (Amidite)

    CAS:
    5'-ODMT cEt G Amidite is a safe, effective nucleic acid analog with strong antisense activity.
    Formula:C46H56N7O9P
    Colore e forma:Solid
    Peso molecolare:881.95
  • 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
    Colore e forma:Solid
    Peso molecolare:611.795
  • PROTAC CDK9 degrader-2

    CAS:
    PROTAC CDK9 degrader-2, potent, selective, IC50 17 μM in MCF-7, wogonin-derived, targets CRBN.
    Formula:C39H36N6O10
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:748.74
  • DSPE-PEG2000-cRGD


    DSPE-PEG2000-cRGD is a PEG compound composed of DSPE and an αvβ3-targeting peptide (cRGD). The cRGD peptide specifically binds to αvβ3 on the surface of various cancer cells and neovascular cells. This compound can be utilized for drug delivery.
    Colore e forma:Odour Solid
  • NUAK1-IN-1


    NUAK1-IN-1 (Compound 9) is an inhibitor of NUAK1 with an IC50 of 5.012 nM, as well as a CDK4 inhibitor. It is suitable for research related to cancer, neurodevelopmental disorders, and Alzheimer's disease.
    Formula:C25H30N6O
    Colore e forma:Solid
    Peso molecolare:430.545
  • CDK12/13-IN-2


    CDK12/13-IN-2 (Compound 24) is a covalent inhibitor of CDK12 and CDK13, exhibiting IC50 values of 15.5 nM and 12.2 nM, respectively. It effectively inhibits the proliferation of breast cancer cells and can be utilized in the research of triple-negative breast cancer.
    Formula:C24H22FN7O2
    Colore e forma:Solid
    Peso molecolare:459.48
  • CD532 hydrochloride


    CD532 hydrochloride, potent Aurora A inhibitor (IC50=45 nM), hampers MYCN protein, changes AURKA's shape, aids cancer research.
    Colore e forma:Solid
  • LDV FITC

    CAS:
    fluorescent ligand that binds to the α4β1 integrin (VLA-4)
    Formula:C69H81N11O17S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:1368.53
  • Anti-MRSA agent 7


    Compound 12: a potent anti-MRSA, inhibits S. aureus/E. coli DNA gyrases/topo IV; IC50: 0.185-0.365/0.341-0.059 μM.
    Formula:C22H20BrF2N3O4
    Colore e forma:Solid
    Peso molecolare:508.31
  • N3,5-Dimethyl-2'-O-(2-methoxyethyl) uridine


    <p>N3,5-Dimethyl-2’-O-(2-methoxyethyl) uridine, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid malignancies.</p>
    Formula:C14H22N2O7
    Colore e forma:Solid
    Peso molecolare:330.33
  • Anti-EMMPRIN/CD147 Antibody


    Anti-EMMPRIN/CD147 Antibody is a human-derived antibody expressed in CHO cells, targeting Basigin. For an isotype control, refer to HumanIgG1kappa, Isotype Control.
    Colore e forma:Odour Liquid
  • dAURK-4

    CAS:
    dAURK-4, a derivative of Alisertib, functions as a potent and selective degrader of AURKA (Aurora A), exhibiting anticancer properties [1].
    Formula:C52H52ClFN8O12
    Colore e forma:Solid
    Peso molecolare:1035.47
  • 11H-Benzo[a]carbazole

    CAS:
    11H-Benzo[a]carbazole is a kinesin-like protein KIF11 inhibitor that can inhibit the viability of HeLa cells.
    Formula:C16H11N
    Purezza:99.14%
    Colore e forma:Solid
    Peso molecolare:217.27
  • Guanosine triphosphate

    CAS:
    Guanosine triphosphate (GTP), a native nucleotide, and its derivatives may serve as specific inhibitors against COVID-19 [1].
    Formula:C10H16N5O14P3
    Colore e forma:Solid
    Peso molecolare:523.18