Ciclo cellulare/Checkpoint
Gli inibitori del ciclo cellulare/dei checkpoint sono composti che interrompono la normale progressione del ciclo cellulare, in particolare nei principali punti di controllo regolatori. Questi inibitori sono fondamentali per studiare la divisione cellulare, comprendere la proliferazione delle cellule cancerose e sviluppare terapie antitumorali. Mirando a fasi specifiche del ciclo cellulare, questi inibitori possono indurre l'arresto del ciclo cellulare, portando all'apoptosi o alla senescenza nelle cellule che si dividono rapidamente. Presso CymitQuimica, offriamo una vasta gamma di inibitori di alta qualità del ciclo cellulare/dei checkpoint per supportare le tue ricerche in biologia del cancro, biologia cellulare e sviluppo di farmaci.
Sottocategorie di "Ciclo cellulare/Checkpoint"
- Chinasi aurora(120 prodotti)
- CDK(561 prodotti)
- Arresto del ciclo cellulare(8 prodotti)
- Chk(49 prodotti)
- DYRK(47 prodotti)
- Dynamin(28 prodotti)
- Ferroptosi(229 prodotti)
- HSP(185 prodotti)
- Integrina(291 prodotti)
- Chinesina(89 prodotti)
- LIM chinasi(22 prodotti)
- Microtubulo associato(286 prodotti)
- PKC(130 prodotti)
- PLK(25 prodotti)
- ROCK(62 prodotti)
- Rho(7 prodotti)
- Wee1(19 prodotti)
- c-Myc(80 prodotti)
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Trovati 2900 prodotti per "Ciclo cellulare/Checkpoint".
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Chk1-IN-6
CAS:Chk1-IN-6 is a potent, selective, and orally bioavailable CHK1 inhibitor candidate.Formula:C16H18F3N7Colore e forma:SolidPeso molecolare:365.3645-Methylcytidine 5′-triphosphate trisodium
5-Methylcytidine 5′-triphosphate trisodium (5-Methyl-CTP trisodium), a modified nucleoside triphosphate, enhances translational properties and stability, whileFormula:C10H15N3Na3O14P3Colore e forma:SolidPeso molecolare:563.13CDK12-IN-4
CAS:CDK12-IN-4 is a pyrazolotriazine that inhibits CDK12 (IC50: 0.641 μM) with high ATP (2 mM) and spares CDK2/Cyclin E and CDK9/Cyclin T1 (IC50: >20 μM).Formula:C20H20F2N8OColore e forma:SolidPeso molecolare:426.4325-Aza-xylo-cytidine
5-Aza-xylo-cytidine, a purine analog with antitumor effects, inhibits DNA synthesis and induces apoptosis in lymphoid cancers.Formula:C8H12N4O5Colore e forma:SolidPeso molecolare:244.2DENV-IN-2
CAS:DENV-IN-2 inhibits dengue virus replication (EC50: 0.016 nM), affects all serotypes (EC50: 0.013-0.029 nM). Derived from WO2018215315A1 6AB.Formula:C29H26ClF3N2O6Colore e forma:SolidPeso molecolare:590.98S-MGB-234 TFA
CAS:S-MGB-234: Novel Minor Groove Binder, potential treatment for animal African trypanosomiasis, effective in mice.Formula:C34H34F6N8O8Colore e forma:SolidPeso molecolare:796.67Apcin A HCL
CAS:Apcin A HCL is an Apcin-derived APC inhibitor that binds Cdc20 and hinders ubiquitination, useful for synthesizing PROTAC CP5V.Formula:C10H15Cl4N5O2Purezza:97.52%Colore e forma:White SolidPeso molecolare:379.07Adenosine Dialdehyde (ADOX)
CAS:Adenosine Dialdehyde, a purine analogue, inhibits SAHH (Ki=3.3 nM), and shows strong anti-tumor effects in vivo.Formula:C10H11N5O4Purezza:95%Colore e forma:SolidPeso molecolare:265.23Ref: TM-T22231
5mg52,00€1mL*10mM (DMSO)57,00€10mg66,00€25mg88,00€50mg155,00€100mg225,00€200mg335,00€500mg565,00€RNA polymerase II-IN-2
RNA Pol II-IN-2 (20iii) strongly inhibits Pol II (Ki=9.5 nM), is more toxic to CHO/HEK293 than α-amanitin.Formula:C41H58N10O12SColore e forma:SolidPeso molecolare:915.02CDK4/6-IN-11
CAS:CDK4/6-IN-11 is a potent PROTAC CDK4/6 degrader.Formula:C43H49N11O7Colore e forma:SolidPeso molecolare:831.92Maleuric acid
CAS:Maleuric acid is an anti-mitotic agent for research and boosts growth and fertility in flora and fauna.Formula:C5H6N2O4Purezza:99.80%Colore e forma:SolidPeso molecolare:158.11Heliquinomycin
CAS:Heliquinomycin, a Streptomyces metabolite, inhibits DNA helicase (Ki=6.8 μM) and fights Gram-positive bacteria and various cancer cells.Formula:C33H30O17Colore e forma:SolidPeso molecolare:698.586CB 3717
CAS:CB 3717 is an enzyme inhibitor, antineoplastic agent, folic acid antagonist.Formula:C24H23N5O6Colore e forma:SolidPeso molecolare:477.471-(β-D-Xylofuranosyl)-N6-Isopentenyladenine
1-(β-D-Xylofuranosyl)-N6-Isopentenyladenine is an adenosine analog.Formula:C15H21N5O4Colore e forma:SolidPeso molecolare:335.36JB300
CAS:JB300 is a PROTAC-based compound that serves as a highly selective degrader of Aurora A, with a DC50 of 30 nM. It is utilized in cancer research. JB300 comprises the PROTAC target protein ligand MK-5108 [pink part], E3 ligase ligand Thalidomide-O-COOH [blue part], and PROTAC Linker Boc-NH-PEG2-C2-NH2 [black part]. The conjugate of the E3 ubiquitin ligase ligand and linker is Thalidomide-O-COOH-NH2-C2-PEG2-NH-Boc.Formula:C43H45ClFN7O10SColore e forma:SolidPeso molecolare:906.375Barasertib
CAS:AZD1152 is a pro-drug of Barasertib (AZD1152)-hQPA. Which is a highly selective Aurora B inhibitor with IC50 of 0.37 nM in a cell-free assay.Formula:C26H31FN7O6PPurezza:99.92% - 99.97%Colore e forma:White SolidPeso molecolare:587.54ddATP tetrasodium
ddATP (2',3'-Dideoxyadenosine 5'-triphosphate) tetrasodium is an active metabolite of 2',3'-dideoxyinosine and functions as a chain elongation inhibitor for DNA polymerase. It is utilized in DNA sequencing using the Sanger method and in research related to viral infections.Formula:C10H12N5Na4O11P3Colore e forma:SolidPeso molecolare:563.11Anticancer agent 263
Anticanceragent 263 (compound 7) is an effective anticancer agent. It binds with the G-quadruplex DNA (G4) sequence 22-mer Pu22 (a c-Myc DNA analog). As a structural modulator, Anticanceragent 263 significantly enhances the formation of protein α-helices and has the capacity to form a supramolecular network. Furthermore, Anticanceragent 263 exhibits no cytotoxicity.Formula:C13H20N2O6Colore e forma:SolidPeso molecolare:300.308Gantofiban
CAS:Gantofiban is a glycoprotein IIb/IIIa (GP IIb/IIIa) antagonist used in the treatment of cardiovascular disease and may be used to study thrombosis.Formula:C21H29N5O6Purezza:99.57%Colore e forma:SolidPeso molecolare:447.48RNA splicing modulator 3
CAS:RNA Splicing Modulator 3 (Compound 236) is an effective RNA splicing modulator, exhibiting an AC50 value of less than 100 nM [1].Formula:C19H20N6OSColore e forma:SolidPeso molecolare:380.47
