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
- CDK
- Cell Cycle Arrest
- Chk
- c-Myc
- Dynamin
- DYRK
- Ferroptosis
- HSP
- Integrin
- Kinesin
- KSP
- LIM Kinase
- Microtubule Associated
- PKC
- PLK
- Rho
- ROCK
- Wee1
Show 11 more subcategories
Products of "Cell Cycle/Checkpoint"
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2'-O-(2-Azidoethyl)adenosine
CAS:2'-O-(2-azidoethyl)adenosine is a purine nucleoside analog with potential antitumor activity.Formula:C12H16N8O4Purity:95%Color and Shape:SolidMolecular weight:336.31N-desmethyl Netupitant
CAS:N-desmethyl Netupitant is a metabolite of Netupitant and a potential Substance-P receptor agonist.Formula:C29H30F6N4OPurity:98%Color and Shape:SolidMolecular weight:564.57PKMYT1-IN-4
PKMYT1-IN-4 (compound 27) functions as a PKMYT1 inhibitor with an IC50 value under 50 nM.Formula:C19H15F3N4O2Color and Shape:SolidMolecular weight:388.34NSC23005
CAS:NSC23005 sodium is a p18INK inhibitor with potently promoted hematopoietic stem cell (HSC) expansion (ED50: 5.21 nM).Formula:C13H17NO4SPurity:99.71%Color and Shape:SolidMolecular weight:283.34WEE1-IN-3
CAS:WEE1-IN-3 (JUN76288) is a potent Wee1 kinase inhibitor with an IC50 of <10 nM. It treatment of cancer and other proliferative diseases.Formula:C28H31N7O2Purity:98.33%Color and Shape:SolidMolecular weight:497.59Ref: TM-T8916
1mg70.00€5mg156.00€10mg239.00€25mg419.00€50mg562.00€100mg810.00€200mg1,074.00€1mL*10mM (DMSO)170.00€A-286982
CAS:A 286982 blocks the LFA-1 and ICAM-1 integrin-ligand interaction.Formula:C24H27N3O4SPurity:97.81%Color and Shape:SolidMolecular weight:453.55Ref: TM-T21781
1mg35.00€2mg50.00€5mg74.00€10mg107.00€25mg210.00€50mg350.00€100mg522.00€1mL*10mM (DMSO)81.00€CDK2-IN-19
CDK2-IN-19 (Compound 32) is a selective, orally active inhibitor of CDK2 (K i: 0.18 nM) that exhibits anticancer activity in mice with OVCAR3 tumors [1].Formula:C20H21FN6O4SPurity:98%Color and Shape:SolidMolecular weight:460.48CC-671
CAS:CC-671 is a dual TTK protein kinase (IC50: 0.005 μM) /CLK2 (IC50: 0.006 μM) inhibitor.Formula:C28H28N6O4Purity:98.35% - 98.65%Color and Shape:SolidMolecular weight:512.56Ref: TM-T4482
1mg52.00€5mg111.00€10mg180.00€25mg359.00€50mg540.00€100mg775.00€500mg1,596.00€1mL*10mM (DMSO)127.00€Rhosin
CAS:Rhosin is a specific inhibitor of RhoA GTPases (Kd: ~0.4 uM), blocking RhoA-GEF interaction, not affecting Cdc42/Rac1/LARG, and induces apoptosis.Formula:C20H18N6OPurity:98%Color and Shape:SolidMolecular weight:358.43MB-PP1
CAS:3MB-PP1 is a bulky purine analog and a Polo-like kinase 1 (Plk1) inhibitor.Formula:C17H21N5Purity:99.97%Color and Shape:White SolidMolecular weight:295.38Ref: TM-T21678
5mg52.00€10mg96.00€25mg170.00€50mg269.00€100mg394.00€500mgTo inquire1mL*10mM (DMSO)58.00€2-Chloropyrazine
CAS:2-Chloropyrazine is used in chemical industry.Formula:C4H3ClN2Purity:98.98% - 99.81%Color and Shape:Clear Colorless To Yellowish LiquidMolecular weight:114.53Trilaciclib
CAS:Trilaciclib is an inhibitor of CDK4/6 (IC50s: 1 nM and 4 nM for CDK4 and CDK6, respectively).Formula:C24H30N8OPurity:98%Color and Shape:SolidMolecular weight:446.55NG 52
CAS:NG 52 (NG-52) is a cell-permeable, reversible, and ATP-compatible inhibitor of the cell cycle-regulating kinase Cdc28p and the related Pho85p kinase.Formula:C16H19ClN6OPurity:98% - 99.36%Color and Shape:SolidMolecular weight:346.81Ref: TM-T2028
1mg74.00€2mg97.00€5mg158.00€10mg269.00€25mg515.00€50mg743.00€100mg1,035.00€500mg2,080.00€1mL*10mM (DMSO)158.00€5-Bromouridine
CAS:5-Bromouridine is a antitumor uracil derivative that induces apoptosis in cancer cells by inhibiting DNA synthesis and is also a marker for DNA and RNA.Formula:C9H11BrN2O6Purity:99.89%Color and Shape:White PowderMolecular weight:323.1CDK9-IN-15
CAS:CDK9-IN-15: potent CDK9 inhibitor, blocks P-TEFb phosphorylation, inhibits transcription, reduces mRNA, induces tumor cell apoptosis.Formula:C16H11N3OSPurity:97.24%Color and Shape:SolidMolecular weight:293.34Ref: TM-T60619
2mg42.00€5mg64.00€10mg97.00€25mg183.00€50mg273.00€100mg393.00€200mg550.00€1mL*10mM (DMSO)62.00€Fosifloxuridine nafalbenamide
CAS:Fosifloxuridine nafalbenamide (NUC 3373), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor.Formula:C29H29FN3O9PPurity:95.87%Color and Shape:SolidMolecular weight:613.53Ref: TM-T33762
1mg88.00€5mg160.00€10mg216.00€25mg393.00€50mg550.00€100mg753.00€500mg1,549.00€1mL*10mM (DMSO)210.00€Retifanlimab
CAS:Retifanlimab (MGA-012) is a monoclonal antibody targeting programmed cell death protein 1 (PD-1). Retifanlimab is used in studies of Merkel cell carcinoma.Purity:95% - 95%Color and Shape:Liquid2'-O-Methyl-2-thiouridine
CAS:2'-O-Methyl-2-thiouridine, a purine nucleoside analog present in synthetic thermophilic bacterial tRNAs, is more selective for A than unmodified U.Formula:C10H14N2O5SPurity:99.89%Color and Shape:SolidMolecular weight:274.292'-O-Methylinosine
CAS:2'-O-Methylinosine (2'-(o-Methyl)-inosine) is an orally bioavailable purine nucleoside analog with antihypertensive activity.Formula:C11H14N4O5Purity:99.88%Color and Shape:SolidMolecular weight:282.25B I09
CAS:B I09, an IRE-1 RNase inhibitor with an IC50 of 1230 nM, inhibits splicing of XBP1 mRNA in human WaC3 cells and expression of xbp-1 in LPS-stimulated B cells.Formula:C16H17NO5Purity:99.23%Color and Shape:SolidMolecular weight:303.31Activated Protein C (390-404), human acetate
Activated Protein C (390-404), human acetate (Activated Protein C ) inhibits APC anticoagulant activity.Formula:C93H134N22O25Purity:99.92%Color and Shape:SolidMolecular weight:1960.19ML-60218
CAS:ML-60218 inhibits RNA pol III in yeast/humans with IC50s of 32/27 μM; disrupts and prevents viroplasms.Formula:C19H15Cl2N3O2S2Purity:98.1%Color and Shape:SolidMolecular weight:452.38Ref: TM-T40661
1mg56.00€5mg119.00€10mg187.00€25mg411.00€50mg638.00€100mg908.00€200mg1,225.00€1mL*10mM (DMSO)131.00€Filanesib
CAS:Filanesib (ARRY 520) is a selective inhibitor of kinesin spindle protein (KSP, IC50 = 6 nM) with potent anti-proliferative activity.Formula:C20H22F2N4O2SPurity:98.06%Color and Shape:SolidMolecular weight:420.48Rabusertib
CAS:Rabusertib (IC-83) is a chk1 inhibitor in trials for various cancers, including pancreatic and non-small cell lung cancer.Formula:C18H22BrN5O3Purity:98.86% - 99.63%Color and Shape:SolidMolecular weight:436.3BMS-1166
CAS:BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor.Formula:C36H33ClN2O7Purity:99.22%Color and Shape:SolidMolecular weight:641.11Ref: TM-T5697
1mg74.00€5mg155.00€10mg225.00€25mg429.00€50mg635.00€100mg944.00€200mg1,264.00€1mL*10mM (DMSO)208.00€6-AZATHYMINE
CAS:6-azathymine inhibits D-3-aminoisobutyrate-pyruvate aminotransferase; 6-azauracil competes with beta-alanine, uncompetitive with pyruvic acid, Ki ~8.9 mM.Formula:C4H5N3O2Purity:99.47%Color and Shape:SolidMolecular weight:127.1CHK1-IN-3
CAS:CHK1-IN-3 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 0.4 nM).Formula:C20H23N9OPurity:98.78%Color and Shape:SolidMolecular weight:405.46Ref: TM-T10791
1mg185.00€2mg279.00€5mg424.00€10mg627.00€25mg938.00€50mg1,311.00€100mg1,795.00€1mL*10mM (DMSO)470.00€Y16 acetate(429653-73-6 free base)
Y16 acetate(429653-73-6 free base) is a G-protein-coupled Rho GEFs inhibitor; works synergistically with Rhosin/G04 in inhibiting LARG-RhoA interaction, RhoAFormula:C51H74N14O13Purity:98%Color and Shape:SolidMolecular weight:1091.24Sangivamycin
CAS:Sangivamycin (NSC-65346) inhibits PKC (Ki=10μM) and hinders growth in various human cancers.Formula:C12H15N5O5Purity:98.11%Color and Shape:SolidMolecular weight:309.28Ref: TM-T9605
1mg126.00€5mg274.00€10mg416.00€25mg677.00€50mg944.00€100mg1,264.00€1mL*10mM (DMSO)360.00€Thiarabine
CAS:Thiarabine displays effective anti-tumor activity. It also inhibition of DNA synthesis.Formula:C9H13N3O4SPurity:98%Color and Shape:SolidMolecular weight:259.28CP-07
CP-07 is a selective and effective PROTAC CDK9 degrader (DC50: 43 nM), demonstrating inhibition of 22RV1 cell proliferation (IC50: 62 nM) and colony formationFormula:C45H48N6O8Purity:98%Color and Shape:SolidMolecular weight:800.95,6-Dihydro-5-methyluracil
CAS:5,6-Dihydro-5-methyluracil (Dihydrothymine) is an intermediate breakdown product of thymine.Formula:C5H8N2O2Purity:98.53%Color and Shape:SolidMolecular weight:128.13Dostarlimab
CAS:Dostarlimab (TSR-042) is an immune checkpoint inhibitor targeting PD-1, blocking its interaction with its ligands PD-L1 and PD-L2.Purity:>95%Color and Shape:LiquidGW406108X(Z/E)
CAS:GW406108X(Z/E) is a mixture of different configurations of GW406108X, which is an inhibitor of Kinesin-12 and ULK1 .Formula:C20H11Cl2NO4Purity:98.23%Color and Shape:SolidMolecular weight:400.21Ref: TM-T9207L
1mg131.00€5mg286.00€10mg430.00€25mg647.00€50mg969.00€100mg1,301.00€1mL*10mM (DMSO)283.00€MBQ-167
CAS:MBQ-167 is a dual inhibitor of Rac/Cdc42 (IC50s: 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively).Formula:C22H18N4Purity:98.07% - 98.74%Color and Shape:SolidMolecular weight:338.41Ref: TM-T16021
1mg37.00€2mg52.00€5mg79.00€10mg111.00€25mg208.00€50mg376.00€100mg567.00€1mL*10mM (DMSO)87.00€RP-6685
CAS:RP-6685 is a potent, selective DNA Polθ inhibitor with strong oral efficacy, an IC50 of 5.8 nM, and marked antitumor effects in mice.Formula:C22H14F7N5OPurity:98.34%Color and Shape:SoildMolecular weight:497.37Ref: TM-T60187
1mg88.00€5mg160.00€10mg230.00€25mg378.00€50mg538.00€100mg755.00€1mL*10mM (DMSO)170.00€dAURK-4 hydrochloride
dAURK-4 hydrochloride, a derivative of Alisertib, functions as a potent and selective degrader of AURKA (Aurora A), exhibiting anticancer properties [1].Formula:C52H53Cl2FN8O12Purity:99.44%Color and Shape:SolidMolecular weight:1071.93CDK9-IN-35
CDK9-IN-35 (compound 10j) acts as an inhibitor of CDK9/CyclinT1, exhibiting an IC50 of 10.2 nM. It also shows an IC50 of 20 nM against the HCT-116 cell line.Formula:C26H24ClFN4O4SColor and Shape:SolidMolecular weight:543.01Anticancer agent 73
CAS:Anticancer agent 73 inhibits TRBP, disrupting TRBP-Dicer, and hinders HCC growth and spread by altering HCC miRNA and protein expression.Formula:C14H15NO4Purity:99.19%Color and Shape:SolidMolecular weight:261.27Rifaximin
CAS:Rifaximin: an oral semi-synthetic antibiotic from rifamycin SV; targets bacterial RNA polymerase to halt growth.Formula:C43H51N3O11Purity:98.05% - 99.40%Color and Shape:Red-Orange Crystalline PowderMolecular weight:785.88Men 10376
CAS:Men 10376 is a selective antagonist of tachykinin NK-2 receptor. It has a Ki of 4.4 μM for rat small intestine NK-2 receptor.Formula:C57H68N12O10Purity:98%Color and Shape:SolidMolecular weight:1081.22Nivolumab
CAS:Nivolumab is a monoclonal antibody, a humanized IgG4 antibody to PD-1. Nivolumab has antitumor activity. Cost-effective and quality-assured.Purity:98% - 98%Color and Shape:LiquidMolecular weight:146 kDa2',3'-Bis-(O-t-butyldimethylsilyl)uridine
CAS:2',3'-Bis-(O-t-butyldimethylsilyl)uridine is a nucleoside derivative protect the NH2/OH groups of nucleosides.inhibitory on viral replication,AIDS and herpes.Formula:C21H40N2O6Si2Purity:99.88%Color and Shape:SolidMolecular weight:472.72Ref: TM-TNU1182
1mg185.00€5mg459.00€10mg657.00€25mg1,026.00€50mg1,415.00€100mg1,872.00€200mg2,555.00€Vitamin D2
CAS:Ergocaliferol (Vitamin D2), derived from ergosterol by UV, inhibits bladder tumor promotion and leukemia, and blocks DNA Polymerase.Formula:C28H44OPurity:98.73% - ≥98%Color and Shape:Prisms From Acetone 1998)Molecular weight:396.65Aurora Kinases-IN-4
CAS:Aurora Kinases-IN-4 (Compound 11c) is a covalent, ATP-competitive inhibitor of aurora kinase A with an IC50 value of 1.7 nM.Formula:C26H28N8OPurity:98%Color and Shape:SolidMolecular weight:468.55P8RI acetate
P8RI acetate mimics CD31, activates CDP8RI, and suppresses the immune response by restoring CD31 pathway.Formula:C53H81N13O11Purity:99.61%Color and Shape:SolidMolecular weight:1076.29Beaucage reagent
CAS:Beaucage reagent, which is found to be effective in causing DNA cleavage.Formula:C7H4O3S2Purity:95.19%Color and Shape:White To Off-White PowderMolecular weight:200.23Abemaciclib metabolite M20
CAS:Abemaciclib metabolite M20 (CDK4/6-IN-4) 是 Abemaciclib 的活性代谢物。 Abemaciclib metabolite M20 是一种特异性 CDK4/6 抑制剂,可用于癌症治疗的相关研究。Formula:C27H32F2N8OPurity:98.32% - 99.29%Color and Shape:SolidMolecular weight:522.59CDK2/Bcl2-IN-1
CDK2/Bcl2-IN-1 (compound 1) is a saponin-based inhibitor of CDK-2 (IC50=117.6 nM) that exhibits potent cytotoxic effects on cancer cells.Formula:C35H56O10SPurity:98%Color and Shape:SolidMolecular weight:668.88
