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"
- Aurora Kinase(121 products)
- CDK(565 products)
- Cell Cycle Arrest(8 products)
- Chk(49 products)
- DYRK(47 products)
- Dynamin(28 products)
- Ferroptosis(234 products)
- HSP(185 products)
- Integrin(293 products)
- Kinesin(89 products)
- LIM Kinase(22 products)
- Microtubule Associated(286 products)
- PKC(130 products)
- PLK(25 products)
- ROCK(61 products)
- Rho(7 products)
- Wee1(19 products)
- c-Myc(82 products)
Show 10 more subcategories
Found 2931 products for "Cell Cycle/Checkpoint".
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Gemifloxacin mesylate
CAS:Gemifloxacin mesylate (Gemifloxacin mesylate) inhibits activities of DNA gyrase and topoisomerase IV, thereby inhibiting DNA replication and eventuallyFormula:C19H24FN5O7SPurity:97.24% - ≥95%Color and Shape:Beige SolidMolecular weight:485.49TAK-901
CAS:TAK-901 has been used in trials studying the treatment of Lymphoma, Myelofibrosis, Multiple Myeloma, Myeloid Metaplasia, and Advanced Solid Tumors, among othersFormula:C28H32N4O3SPurity:99.02% - 99.59%Color and Shape:Yellow SolidMolecular weight:504.64Ref: TM-T2709
1mg34.00€5mg66.00€1mL*10mM (DMSO)74.00€10mg99.00€25mg192.00€50mg313.00€100mg497.00€200mg710.00€Metarrestin
CAS:Metarrestin (ML246) is a first-in-class perinucleolar compartment inhibitor with a favorable PK profile, which effectively suppresses metastasis.Formula:C31H30N4OPurity:99.45%Color and Shape:White SolidMolecular weight:474.6Ref: TM-T12006
1mg38.00€2mg50.00€5mg84.00€1mL*10mM (DMSO)87.00€10mg137.00€25mg281.00€50mg485.00€100mg700.00€500mg1,459.00€Nedaplatin
CAS:Nedaplatin, a cisplatin derivative, induces tumor DNA damage (IC50: 94 μM) through platinum-DNA cross-links, causing apoptosis.Formula:C2H8N2O3PtPurity:99.88% - >99.99%Color and Shape:SolidMolecular weight:303.17Trilaciclib hydrochloride
CAS:Trilaciclib hydrochloride (G1T28 hydrochloride) is an inhibitor of CDK4/6 (IC50s: 1 nM and 4 nM for CDK4 and CDK6).Formula:C24H32Cl2N8OPurity:99.69% - 99.89%Color and Shape:SolidMolecular weight:519.47NU6140
CAS:NU6140 is a selective inhibitor of CDK2-cyclin A (IC50, 0.41 μM).Formula:C23H30N6O2Purity:98.33%Color and Shape:SolidMolecular weight:422.52Ref: TM-T16359
2mg39.00€5mg60.00€1mL*10mM (DMSO)67.00€10mg92.00€25mg177.00€50mg285.00€100mg414.00€200mg580.00€Ribociclib succinate
CAS:Ribociclib succinate (LEE011 succinate) is a highly specific CDK4/6 inhibitor (IC50: 10 nM and 39 nM, respectively).Formula:C27H36N8O5Purity:99.90%Color and Shape:White SolidMolecular weight:552.63R-10015
CAS:R-10015, potent LIMK inhibitor with 38 nM IC50 for LIMK1, targets ATP pocket, and serves as a broad-spectrum HIV antiviral.Formula:C20H19ClN6O2Purity:98.68%Color and Shape:SolidMolecular weight:410.86Ref: TM-T12609
1mg50.00€5mg112.00€1mL*10mM (DMSO)124.00€10mg170.00€25mg280.00€50mg371.00€100mg525.00€200mg712.00€XPW1
CAS:XPW1 is a CDK9 inhibitor with antitumor activity, inhibits DNA repair procedures, and can be used for the research of clear cell renal cell carcinoma.Formula:C36H39ClFN7O2Purity:99.63%Color and Shape:White SolidMolecular weight:656.19Ref: TM-T77810
10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire200mgTo inquire1mg77.00€5mg167.00€AZ1495
CAS:AZ1495: oral IRAK4 inhibitor (IC50: 5 nM), IRAK1 (23 nM), treats MYD88L265P DLBCL.Formula:C21H31N5O2Purity:98.81%Color and Shape:SolidMolecular weight:385.5Ref: TM-T14367
1mg93.00€5mg156.00€1mL*10mM (DMSO)170.00€10mg245.00€25mg349.00€50mg494.00€100mg750.00€200mg1,009.00€Enrofloxacin
CAS:Enrofloxacin (BAY-Vp2674) is a veterinary antibacterial agent, used in poultry.Formula:C19H22FN3O3Purity:99.43% - >99.99%Color and Shape:White SolidMolecular weight:359.39BMT-124110 Formate
BMT-124110 Formate is a selective AAK1 inhibitor (IC50: 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinaseFormula:C22H20N2O2Purity:98.62%Color and Shape:White SolidMolecular weight:344.41Ref: TM-T10572L
1mg175.00€5mg388.00€1mL*10mM (DMSO)404.00€10mg572.00€25mg888.00€50mg1,224.00€100mg1,648.00€500mg3,312.00€CDK2-IN-4
CAS:CDK2-IN-4 is a potent and selective inhibitor of CDK2 with an IC50 of 44 nM for CDK2/cyclin A.Formula:C23H18N6O2SPurity:97.24% - 99.10%Color and Shape:SolidMolecular weight:442.49Ref: TM-T14916
1mg82.00€5mg192.00€1mL*10mM (DMSO)212.00€10mg304.00€25mg522.00€50mg713.00€100mg1,018.00€Hycanthone
CAS:Hycanthone (Etrenol(mesylate)) is a potent drug of antischistosomal.Formula:C20H24N2O2SPurity:98.78%Color and Shape:Yellow-Orange Powder (Ntp 1992)Molecular weight:356.48GSK-1520489A
CAS:GSK-1520489A is an active PKMYT1 inhibitor.Formula:C21H23N5O3SPurity:99.85%Color and Shape:White SolidMolecular weight:425.5JH-RE-06
CAS:JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POLζ.Formula:C20H16Cl3N3O4Purity:99.29%Color and Shape:SolidMolecular weight:468.72Mps1-IN-3
CAS:Mps1-IN-3 is an effective and selective inhibitor of MPS1 kinase (IC50: 50 nM).Formula:C26H31N7O4SPurity:99.25%Color and Shape:SolidMolecular weight:537.63Ref: TM-T16130
2mg34.00€5mg54.00€1mL*10mM (DMSO)64.00€10mg87.00€25mg149.00€50mg255.00€100mg384.00€200mg538.00€MF-094
CAS:MF-094 is a selective USP30 inhibitor with IC50 of 0.12 μM. MF-094 can increase protein ubiquitination and accelerate mitophagy.Cost-effective and quality-assured.Formula:C30H37N3O4SPurity:99.93%Color and Shape:White SolidMolecular weight:535.7Ref: TM-T12024
1mg40.00€5mg93.00€1mL*10mM (DMSO)99.00€10mg137.00€25mg268.00€50mg430.00€100mg620.00€200mg884.00€SU056
CAS:SU056 is a YB-1 inhibitor that induces cell-cycle arrest, apoptosis, and inhibits ovarian cancer cell migration.Formula:C20H16FNO5Purity:99.89%Color and Shape:Yellow SolidMolecular weight:369.34MYCi975
CAS:MYCi975 (NUCC-0200975) is an orally active inhibitor of MYC.Formula:C25H16Cl2F6N2O2Purity:99.3% - 99.82%Color and Shape:SolidMolecular weight:561.303
