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(114 products)
- CDK(543 products)
- Cell Cycle Arrest(5 products)
- Chk(47 products)
- DYRK(48 products)
- Dynamin(27 products)
- Ferroptosis(226 products)
- HSP(179 products)
- Integrin(228 products)
- Kinesin(88 products)
- LIM Kinase(20 products)
- Microtubule Associated(274 products)
- PKC(119 products)
- PLK(25 products)
- ROCK(63 products)
- Rho(5 products)
- Wee1(14 products)
- c-Myc(76 products)
Show 10 more subcategories
Found 3826 products of "Cell Cycle/Checkpoint"
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TCRS-417
CAS:TCRS-417 (T417) inhibits PBX1-DNA interaction in mammalian cells or cell clusters, used in autoimmune and neurodegenerative disease research.Formula:C25H19FN2O5Color and Shape:SolidMolecular weight:446.43N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methylcytidine
CAS:Nucleoside Derivatives - 2’-Modified nucleoside, Protected nucleosides with NH2/OH open; Ready for phosphorylationFormula:C41H43N3O9Color and Shape:SolidMolecular weight:721.79Ref: TM-TNU1115
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquire(S)-GNA-G(iBu) phosphoramidite
CAS:(S)-GNA-G(iBu) phosphoramidite is a Nucleoside Derivative - Acyclic nucleoside;Nucleoside Phosphoramidite.Formula:C42H52N7O7PColor and Shape:SolidMolecular weight:797.88Ref: TM-TNU1440
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquireX5050
CAS:X5050 is a REST inhibitor, with an EC 50 of 2.1 μM.Formula:C17H15N3O3Color and Shape:SolidMolecular weight:309.325Cytidine (Standard)
CAS:Cytidine (Standard) is the standard substance of Cytidine, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Cytidine (Cytosine-1-β-D-ribofuranoside) is a pyrimidine nucleoside comprised of a cytosine bound to ribose via a beta-N1-glycosidic bond. Cytidine is a precursor for uridine. Both cytidine and uridine are utilized in RNA synthesis.Formula:C9H13N3O5Color and Shape:Physical Description White Crystalline Powder (Ntp 1992)Molecular weight:243.225-Bromocytidine
CAS:5-Bromocytidine is a nucleoside analog that is a key disinfection by-product of drinking water and may interfere with nucleic acid synthesis.Formula:C9H12BrN3O5Purity:99.63%Color and Shape:SolidMolecular weight:322.115'-O-(4,4'-Dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine
CAS:5'-O-(4,4'-Dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine is a Nucleoside Derivative - 2'-Modified nucleoside; Protected nucleoside with NH2/OH open;Formula:C34H38N2O9Color and Shape:SolidMolecular weight:618.67Ref: TM-TNU1094
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquireCeftriaxone Sodium
CAS:Ceftriaxone Sodium is a sporotaxin antibiotic that inhibits GSK3β and Aurora B. It is used in the study of sepsis and infective endocarditis.Formula:C18H17N8NaO7S3Color and Shape:SolidMolecular weight:576.5622'-Amino-2'-deoxy-b-D-arabino-5-methyl uridine
CAS:2'-Amino-2'-deoxy-b-D-arabino-5-methyl uridine is a purine nucleoside analog with potential antitumor activity.Formula:C10H15N3O5Purity:96.76%Color and Shape:SolidMolecular weight:257.24VP-U-6
CAS:VP-U-6 is a Nucleoside Phosphoramidite; Nucleoside Derivative - Phosphorus-containing nucleotide; 5'-Modified nucleoside.Formula:C24H40N4O9P2Color and Shape:SolidMolecular weight:590.54Ref: TM-TNU1009
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire500mgTo inquireDOTA-cyclo(RGDfK)
CAS:DOTA-cyclo(RGDfK) is a and DOTA-like chelator peptide,the αvβ3 integrin receptor ,radionuclide coupled compounds RDCs cancer diagnostics and therapy.Formula:C43H67N13O14Color and Shape:SoildMolecular weight:990.078-Hydroxyadenosine
CAS:8-Hydroxyadenosine (8-Oxoadenosine) is a purine nucleoside found in Torula yeast RNA.Formula:C10H13N5O5Purity:99.71%Color and Shape:SolidMolecular weight:283.24Verosudil
CAS:Verosudil (AR-12286), a ROCK1/2 inhibitor (Ki: 2 nM), lowers intraocular pressure in mice by enhancing aqueous outflow.Formula:C17H17N3O2SPurity:99.68%Color and Shape:SolidMolecular weight:327.4Ref: TM-T60924
1mg55.00€5mg147.00€10mg231.00€25mg370.00€50mg522.00€100mg692.00€1mL*10mM (DMSO)161.00€A-674563
CAS:A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.Formula:C22H22N4OPurity:99.21%Color and Shape:SolidMolecular weight:358.44GSK269962A hydrochloride
CAS:GSK269962A hydrochloride (GSK 269962 hydrochloride) is a ROCK inhibitor with anti-inflammatory and vasodilatory effects and inhibits ROCK1 and ROCK2.Formula:C29H31ClN8O5Color and Shape:SolidMolecular weight:607.06TG-693
CAS:TG-693, Oral CLK1 inhibitor, promotes exon 31 skipping of dystrophin gene, inhibits CLK1 substrate phosphorylation, for Duchenne muscular dystrophy.Formula:C12H9N3Purity:99.81%Molecular weight:195.23GPRP
CAS:GPRP (Gly-Pro-Arg-Pro) is a fibrin polymerization inhibitor.Formula:C18H31N7O5Color and Shape:White To Off-White PowderMolecular weight:425.48STD1T
CAS:STD1T is a USP2a inhibitor with anticancer activity that reduces levels of the cell cycle protein D1 protein in HCT116 colon cancer cells.Formula:C19H19N3O4S2Purity:98.77%Color and Shape:SolidMolecular weight:417.5PROTAC CDK9 Degrader-1
CAS:PROTAC CDK9 Degrader-1 is a selective PROTAC-based CDK9 degrader, composed of a Cereblon ligand and a CDK ligand.Formula:C33H35N5O7Purity:95.1%Color and Shape:SolidMolecular weight:613.66USP8-IN-1
CAS:USP8-IN-1 is an inhibitor of USP8 with an IC 50 of 1.9 μM. USP8-IN-1 inhibits H1975 cell growth with a GI 50 of 82.04 μM [1].Formula:C18H21N5O3SPurity:99.07%Color and Shape:SoildMolecular weight:387.46Ref: TM-T60146
1mg84.00€5mg177.00€10mg250.00€25mg439.00€50mg620.00€100mg893.00€1mL*10mM (DMSO)195.00€
