CymitQuimica logo
Chk

Chk

Chk (Checkpoint Kinase) inhibitors target the Chk1 and Chk2 kinases, which are key regulators of the DNA damage response and cell cycle checkpoints. These kinases halt cell cycle progression in response to DNA damage, allowing time for repair. Inhibiting Chk kinases can prevent cell cycle arrest, forcing damaged cells to proceed through the cycle and ultimately undergo apoptosis. Chk inhibitors are particularly valuable in cancer research, where they can sensitize tumor cells to DNA-damaging agents. At CymitQuimica, we provide a variety of high-quality Chk inhibitors to support your research in DNA damage response, cell cycle regulation, and oncology.

Found 42 products of "Chk"

Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
  • CHK1-IN-4 hydrochloride


    <p>CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1).</p>
    Formula:C18H19BrClN7O2
    Purity:99.29%
    Color and Shape:Soild
    Molecular weight:480.75
  • Monalizumab

    CAS:
    <p>Monalizumab, a humanized antibody, enhances NK cell function by inhibiting NKG2A; used in HNSCC studies.</p>
    Purity:95% - > 95%
    Color and Shape:Liquid
    Molecular weight:147 kDa (average)
  • WAY-230563

    CAS:
    <p>WAY-230563 is a serine/threonine kinase inhibitor that blocks CHK1/CHK2-mediated cell cycle checkpoints, leading to G2/M phase arrest in tumour cells</p>
    Formula:C17H12N2O2S
    Purity:98.40%
    Color and Shape:Solid
    Molecular weight:308.35
  • CBP501 Affinity Peptide

    CAS:
    <p>CBP501 Affinity Peptide, a Chk kinase inhibitor, disrupts G2 arrest triggered by DNA-damaging agents and is utilized in cancer research [1].</p>
    Formula:C68H119N21O25S
    Color and Shape:Solid
    Molecular weight:1662.86
  • Zimistobart

    CAS:
    <p>Zimistobart (BMS-986315) is a fully human IgG1 antibody that targets and binds to NKG2A. It is applicable in research for non-small cell lung cancer (NSCLC). For an isotype control, refer to HumanIgG1kappa, Isotype Control.</p>
    Color and Shape:Liquid
  • CCT241533 dihydrochloride

    CAS:
    <p>Potent Chk2 inhibitor with 3 nM IC50, 63-fold more selective over Chk1, affects 84 kinases, reduces DNA damage response and apoptosis in cells.</p>
    Formula:C23H29Cl2FN4O4
    Color and Shape:Solid
    Molecular weight:515.41
  • Chk1-IN-6

    CAS:
    <p>Chk1-IN-6 is a potent, selective, and orally bioavailable CHK1 inhibitor candidate.</p>
    Formula:C16H18F3N7
    Color and Shape:Solid
    Molecular weight:365.364
  • CHK1-IN-12


    <p>CHK1-IN-12 (Compound example 1-5) is a highly selective and orally active checkpoint kinase 1 (CHK1) inhibitor, demonstrating an in vitro enzyme IC50 of ≤10 nM and a cellular IC50 of ≤50 nM. This compound suppresses the phosphorylation activity of CHK1 kinase, disrupts DNA damage response pathways, and induces tumor cell cycle arrest and apoptosis. CHK1-IN-12 shows promise for cancer research applications.</p>
    Formula:C19H19N7O2
    Color and Shape:Solid
    Molecular weight:377.16002
  • CHK1-IN-9


    <p>CHK1-IN-9 (compound 11) is an orally active CHK1 inhibitor with an IC50 of 0.55 nM. It enhances the effects of DNA-damaging agents on tumor cells and exhibits synergistic anticancer activity with Gemcitabine.</p>
  • CCT244747

    CAS:
    <p>CCT244747 is a potent and selective CHK1 inhibitor oral, ATP-competitive, and cytotoxic, abrogating drug-induced S and G2 blockade and inducing apoptosis .</p>
    Formula:C20H24N8O2
    Purity:99.17%
    Color and Shape:Solid
    Molecular weight:408.46
  • GDC-0425

    CAS:
    <p>GDC-0425 (RG-7602), an oral selective ChK1 inhibitor, targets multiple cancers.</p>
    Formula:C18H19N5O
    Color and Shape:Solid
    Molecular weight:321.38
  • GDC-0575 dihydrochloride

    CAS:
    <p>GDC-0575 dihydrochloride (ARRY-575 dihydrochloride) is a selective, orally active CHK1 inhibitor (IC50: 1.2 nM) that exhibits antitumour effects.</p>
    Formula:C16H22BrCl2N5O
    Color and Shape:Solid
    Molecular weight:451.19
  • LY2880070

    CAS:
    <p>LY2880070 is a new checkpoint kinase 1 (CHK1) inhibitor for cancer therapy.</p>
    Formula:C19H23N7O2
    Purity:99.77%
    Color and Shape:Solid
    Molecular weight:381.43
  • GDC-0575

    CAS:
    <p>GDC-0575 (ARRY-575) is a highly-selective oral small-molecule Chk1 inhibitor(IC50 of 1.2 nM).</p>
    Formula:C16H20BrN5O
    Purity:≥95%
    Color and Shape:Solid
    Molecular weight:378.27
  • SCH900776

    CAS:
    <p>SCH900776 (MK-8776) is an agent targeting cell cycle checkpoint kinase 1 (Chk1) with potential radiosensitization and chemosensitization activities.</p>
    Formula:C15H18BrN7
    Purity:96.69% - 99.6%
    Color and Shape:Solid
    Molecular weight:376.25
  • GDC0575 monohydrochloride

    CAS:
    <p>GDC0575 (ARRY575), a potent Chk1 inhibitor, IC50 1.2nM, disrupts cell cycle arrest, allowing DNA repair before mitosis.</p>
    Formula:C16H21BrClN5O
    Purity:97.85%
    Color and Shape:Solid
    Molecular weight:414.73
  • SAR-020106

    CAS:
    <p>SAR-020106 is a potent, ATP-competitive, and selective CHK1 inhibitor with an IC50 of 13.3 nmol/L on the isolated human enzyme.</p>
    Formula:C19H19ClN6O
    Purity:97.78%
    Color and Shape:Solid
    Molecular weight:382.85
  • Rabusertib

    CAS:
    <p>Rabusertib (IC-83) is a chk1 inhibitor in trials for various cancers, including pancreatic and non-small cell lung cancer.</p>
    Formula:C18H22BrN5O3
    Purity:98.86% - 99.87%
    Color and Shape:Solid
    Molecular weight:436.3
  • CCT245737

    CAS:
    <p>CCT245737 is an orally active, selective Chk1 inhibitor, and is &gt;1,000-fold selective over CHK2 and CDK1.Cost-effective and quality-assured.</p>
    Formula:C16H16F3N7O
    Purity:98.06% - 99.69%
    Color and Shape:Solid
    Molecular weight:379.34
  • AZD-7762

    CAS:
    <p>AZD-7762, an effective and specific inhibitor of Chk1(IC50=5 nM), is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.</p>
    Formula:C17H19FN4O2S
    Purity:98.96% - 99.19%
    Color and Shape:Solid
    Molecular weight:362.42
  • AZD7762 HCl

    CAS:
    <p>AZD7762 HCl is a checkpoint kinase inhibitor, driving checkpoint abrogation and enhancing DNA-targeted treatment.</p>
    Formula:C17H20ClFN4O2S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:398.88
  • PV-1115

    CAS:
    <p>PV-1115 is an effective and highly selective inhibitor of the Chk2.</p>
    Formula:C20H19N7O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:405.41
  • NSC 109555 ditosylate

    CAS:
    <p>Chk2 inhibitor,ATP-competitive</p>
    Formula:C26H32N10O4S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:580.66
  • PV-1019

    CAS:
    <p>PV-1019 (NSC 744039), a potent Chk2 inhibitor, has an IC50 of 24 nM and blocks Chk2 autophosphorylation and IR-induced apoptosis.</p>
    Formula:C18H17N7O3
    Color and Shape:Solid
    Molecular weight:379.37
  • VRX-0466617

    CAS:
    <p>VRX-0466617 is a novel selective Chk2 inhibitor.</p>
    Formula:C19H20BrN5O2S
    Color and Shape:Solid
    Molecular weight:462.36
  • TCS 2312

    CAS:
    <p>checkpoint kinase 1 (chk1) inhibitor</p>
    Formula:C25H24N4O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:412.48
  • SC-203885

    CAS:
    <p>SC-203885 is a checkpoint kinase 2 inhibitor.</p>
    Formula:C15H13N5O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:295.3
  • M443

    CAS:
    <p>M443 is a potent small molecule inhibitor of MRK that inhibits radiation-induced activation of p38 and Chk2 and can be used in cancer research.</p>
    Formula:C31H30F3N7O2
    Purity:98.95%
    Color and Shape:Solid
    Molecular weight:589.61
  • NR2F6 modulator-1

    CAS:
    <p>NR2F6 modulator-1, a potent agent for NR2F6, affects immune response and tumor stem cell activity.</p>
    Formula:C23H17NO5S
    Purity:98.31%
    Color and Shape:Solid
    Molecular weight:419.45
  • CHK1-IN-3

    CAS:
    <p>CHK1-IN-3 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 0.4 nM).</p>
    Formula:C20H23N9O
    Purity:98.78%
    Color and Shape:Solid
    Molecular weight:405.46
  • CCT241533 hydrochloride

    CAS:
    <p>CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).</p>
    Formula:C23H28ClFN4O4
    Purity:97.13%
    Color and Shape:Solid
    Molecular weight:478.95
  • MU-380

    CAS:
    <p>MU-380 is an effective and selective inhibitor of CHK1.</p>
    Formula:C15H15BrF3N7
    Color and Shape:Solid
    Molecular weight:430.23
  • CCT241533

    CAS:
    <p>CCT241533 is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).</p>
    Formula:C23H27FN4O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:442.48
  • VER-00158411

    CAS:
    <p>VER-00158411 is a checkpoint kinase 1 and CHK2 inhibitor (IC50: 4.4 nM and 4.5 nM, respectively).</p>
    Formula:C31H34N6O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:538.64
  • CHK1-IN-2

    CAS:
    <p>CHK1-IN-2 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 6 nM).</p>
    Formula:C20H22N4OS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:366.48
  • CHK1-IN-4

    CAS:
    <p>CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.</p>
    Formula:C18H18BrN7O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:444.29
  • CHK-IN-1

    CAS:
    <p>CHK-IN-1 is a dual inhibitor of CHK1 and CHK2 with antiproliferative activity.</p>
    Formula:C18H19ClFN5OS
    Purity:>99.99%
    Color and Shape:Solid
    Molecular weight:407.89
  • BBI-355

    CAS:
    <p>BBI-355 is an oral, potent, and selective small molecule CHK1 inhibitor with an IC50 of 0.3 nM. It exhibits significant antitumor activity, both as a monotherapy and in combination with targeted therapies, across various ecDNA+ oncogene-amplified tumor models.</p>
    Formula:C19H19N7O2
    Color and Shape:Solid
    Molecular weight:377.40
  • CHK1-IN-11

    CAS:
    <p>CHK1-IN-11 (Compound 1) is an orally active inhibitor of checkpoint kinase 1 (CHK1). It is utilized in research focused on cancers with oncogene amplification.</p>
    Formula:C20H22N8O2
    Color and Shape:Solid
    Molecular weight:406.44
  • CHK1 inhibitor

    CAS:
    <p>CHK1 inhibitor (GDC-0575 analog) is a CHK1 inhibitor.</p>
    Formula:C17H21BrN4O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:377.28
  • Chk1-IN-5

    CAS:
    <p>Chk1-IN-5 inhibits Chk1, blocking phosphorylation and suppressing colon cancer growth.</p>
    Formula:C18H18FN7O2
    Color and Shape:Solid
    Molecular weight:383.38
  • PHI-101

    CAS:
    <p>PHI-101 is a checkpoint kinase 2 (Chk2) inhibitor that can be used for the study of refractory acute myeloid leukemia (AML) and ovarian cancer.</p>
    Formula:C19H19FN4O2S
    Purity:99.4%
    Color and Shape:Solid
    Molecular weight:386.44

    Ref: TM-T81490

    1mg
    Discontinued
    5mg
    Discontinued
    10mg
    Discontinued
    25mg
    Discontinued
    50mg
    Discontinued
    100mg
    Discontinued
    200mg
    Discontinued
    1mL*10mM (DMSO)_old
    Discontinued
    Discontinued product