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PLK

PLK

Gli inibitori delle chinasi Polo-like (PLK) prendono di mira le PLK, una famiglia di chinasi serina/treonina essenziali per varie fasi della divisione cellulare, tra cui l'ingresso in mitosi, l'assemblaggio del fuso e la citocinesi. Le PLK sono fondamentali per la corretta esecuzione del ciclo cellulare e la loro disregolazione è spesso associata al cancro. L'inibizione delle PLK può indurre l'arresto del ciclo cellulare e l'apoptosi nelle cellule tumorali, rendendo questi inibitori strumenti importanti nella ricerca e nella terapia del cancro. Presso CymitQuimica, offriamo una gamma di inibitori delle PLK di alta qualità per supportare la tua ricerca sulla mitosi, il controllo del ciclo cellulare e l'oncologia.

Trovati 25 prodotti di "PLK"

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  • SP27


    <p>SP27, a selective PROTAC, degrades PLK4 with a DC50 of 19.5 nM and may be utilized in breast cancer research [1].</p>
    Formula:C40H40F2N12O5
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:806.82
  • RP-1664

    CAS:
    <p>RP-1664,PLK4 inhibitor (IC50=3 nM). Disrupts centriole biogenesis. Antitumor activity in breast cancer, neuroblastoma.</p>
    Formula:C23H24F2N8O2S
    Purezza:99.04%
    Colore e forma:Soild
    Peso molecolare:514.55
  • PLK1-IN-12


    PLK1-IN-12 is a highly selective, orally active PLK1 inhibitor with an IC50 of 20 nM. It demonstrates greater selectivity for PLK1 over PLK2 (IC50: >10000 nM) and PLK3 (IC50: 3953 nM). PLK1-IN-12 exhibits anticancer efficacy across a wide range of cell lines and is applicable to anti-leukemia research.
    Colore e forma:Odour Solid
  • PLK1-IN-14


    PLK1-IN-14 (Compound Hit-4) is a selective PLK1 inhibitor with an IC50 of 22.61 pM for PLK1, and an IC50 of 0.09 nM for inhibiting the proliferation of DU-145 prostate cancer cells. It is applicable in prostate cancer research.
    Colore e forma:Odour Solid
  • PLK1 Protein, Mouse, Recombinant (His)


    PLK1 Protein, Mouse, Recombinant (His) is expressed in Baculovirus insect cells with His tag.
    Colore e forma:Lyophilized Powder
    Peso molecolare:70.6 kDa (predicted); 65 kDa (reducing conditions)
  • Poloxime

    CAS:
    Poloxime is a hydrolysis product of poloxin and is a non-ATP-competitive Plk1 inhibitor. It also has moderate Plk1 inhibitory activity.
    Formula:C10H13NO2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:179.22
  • PLK1 Protein, Human, Recombinant (His)


    PLK1 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag.
    Purezza:96.8%
    Colore e forma:Lyophilized Powder
    Peso molecolare:70.5 kDa (predicted); 66 kDa (reducing conditions)
  • 5-ETHYL-4,5,6,7-TETRAHYDRO-THIAZOLO[5,4-C]PYRIDIN-2-YLAMINE

    CAS:
    5-ETHYL-4,5,6,7-TETRAHYDRO-THIAZOLO[5,4-C]PYRIDIN-2-YLAMINE targets PLK1.
    Formula:C8H13N3S
    Purezza:99.03%
    Colore e forma:Solid
    Peso molecolare:183.27
  • MLN0905

    CAS:
    MLN0905 (PLK1 Inhibitor) is an effective PLK1 inhibitor(IC50=2 nM).
    Formula:C24H25F3N6S
    Purezza:98% - 99.92%
    Colore e forma:Solid
    Peso molecolare:486.56
  • GSK461364

    CAS:
    GSK461364 (GSK461364A)(Ki=2.2 nM) inhibits purified Plk1 .The specificity of GSK461364 for Plk1 is more than 1000-fold over Plk2/3.
    Formula:C27H28F3N5O2S
    Purezza:99% - 99.73%
    Colore e forma:Solid
    Peso molecolare:543.6
  • HMN-176

    CAS:
    <p>HMN-176 is a stilbene derivative which inhibits mitosis, interfering with polo-like kinase-1 (plk1).</p>
    Formula:C20H18N2O4S
    Purezza:98.92% - 98.99%
    Colore e forma:Solid
    Peso molecolare:382.43
  • (1E)-CFI-400437 dihydrochloride

    CAS:
    (1E)-CFI-400437 dihydrochloride (CFI-400437 dihydrochloride) is a selective and potent polo-like kinase 4 (PLK4) inhibitor.
    Formula:C29H30Cl2N6O2
    Purezza:97.08%
    Colore e forma:Solid
    Peso molecolare:565.5
  • Poloxin

    CAS:
    <p>Poloxin is a non-ATP competitive Polo-like Kinase 1 inhibitor. It targets the polo-box domain (IC50: appr 4.8 μM).</p>
    Formula:C18H19NO3
    Purezza:99.19%
    Colore e forma:Solid
    Peso molecolare:297.35
  • HMN-214

    CAS:
    HMN-214 (IVX-214) is a potent PLK1 inhibitor with an average IC50 of 0.12 μM.
    Formula:C22H20N2O5S
    Purezza:98% - >99.99%
    Colore e forma:Solid
    Peso molecolare:424.47
  • TAK-960

    CAS:
    <p>TAK-960 is an orally bioavailable, selective inhibitor of Plks with IC50 values of 0.8, 16.9, and 50.2 nM for Plk1, Plk2, and Plk3, respectively.</p>
    Formula:C27H34F3N7O3
    Purezza:97.06%
    Colore e forma:Solid
    Peso molecolare:561.6
  • Ro3280

    CAS:
    Ro3280 (Ro5203280) is an effective, specific inhibitor of PLK1(IC50=3, Kd=0.09 nM).
    Formula:C27H35F2N7O3
    Purezza:97.1% - >99.99%
    Colore e forma:Solid
    Peso molecolare:543.61
  • Centrinone-B

    CAS:
    Centrinone-B (LCR-323) is a Plk4 inhibitor with potential anticancer activity for the study of triple-negative breast cancer.
    Formula:C27H27F2N7O5S2
    Purezza:98.71%
    Colore e forma:Solid
    Peso molecolare:631.67
  • Cyclapolin 9

    CAS:
    Cyclapolin 9: Selective PLK1 inhibitor, IC50 500 nM, ATP-competitive, inactive against other kinases.
    Formula:C9H4F3N3O4S
    Purezza:99.64%
    Colore e forma:Solid
    Peso molecolare:307.21
  • Poloxin-2

    CAS:
    <p>Poloxin-2 is a potent and selective Plk1 PBD inhibitor with anti-tumour activity that reduces the protein level of Plk1 in HeLa cells.</p>
    Formula:C16H15NO3
    Purezza:99.67%
    Colore e forma:Solid
    Peso molecolare:269.3
  • TC-S 7005

    CAS:
    TC-S 7005 is an effective inhibitor of Polo-like kinases (IC50s: 214 nM, 4 nM and 24 nM for Plk1, Plk2, and Plk3).
    Formula:C21H17N3O3
    Purezza:99.516%
    Colore e forma:Solid
    Peso molecolare:359.38