ATM/ATR
Gli inibitori di ATM (Ataxia Telangiectasia Mutated) e ATR (ATM and Rad3-related) prendono di mira chinasi chiave coinvolte nella risposta al danno al DNA (DDR) che vengono attivate in risposta a rotture del doppio filamento di DNA e stress da replicazione. Questi inibitori interrompono la capacità di queste chinasi di rilevare e riparare i danni al DNA, il che può portare a un aumento dell'instabilità genomica e alla morte cellulare, in particolare nelle cellule tumorali che dipendono da robusti meccanismi di riparazione del DNA per sopravvivere. Gli inibitori di ATM/ATR sono strumenti cruciali nella ricerca e nella terapia del cancro, soprattutto in combinazione con agenti che danneggiano il DNA. Presso CymitQuimica, offriamo una vasta gamma di inibitori di ATM/ATR di alta qualità per supportare la tua ricerca sulla risposta al danno al DNA, la biologia del cancro e lo sviluppo terapeutico.
Trovati 78 prodotti per "ATM/ATR".
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FEN1-IN-1
CAS:FEN1-IN-1 (LNT-1), a FEN1 active site inhibitor, partly works by coordinating Mg2+ ions.Formula:C15H12N2O5SPurezza:99.72% - 99.93%Colore e forma:White SolidPeso molecolare:332.331Garcinone C
CAS:Garcinone C, a xanthone from Garcinia oblongifolia, is anti-inflammatory, promotes healing, and may fight some cancers.Formula:C23H26O7Purezza:99.13% - 99.92%Colore e forma:Yellow SolidPeso molecolare:414.4483Elimusertib hydrochloride
Elimusertib hydrochloride(1876467-74-1 free base) (BAY-1895344 hydrochloride) is a effective, orally available and selective ATR inhibitor with anti-tumorFormula:C20H22ClN7OPurezza:98.8% - 99.03%Colore e forma:SolidPeso molecolare:411.89Antitumor agent-28
CAS:Antitumor agent-28 inhibits ATM kinase, blocking ATM disease progression and showing anti-cancer effects.Formula:C25H32N6O4SColore e forma:SolidPeso molecolare:512.63ATM Inhibitor-6
CAS:ATM inhibitor-6 (A-193), a selective inhibitor of ATM kinase, is utilized in cancer research [1].Formula:C28H33FN6O2Peso molecolare:504.60ATR kinase substrate peptide
ATRkinase substrate peptide (compound 45) is a potent and selective inhibitor of the ATR protein kinase, with a Ki of 6 nM. It inhibits ATR activity by competing with the ATP binding site of the ATR kinase, thereby blocking ATR-mediated signal transduction. This compound can be utilized to study the role of ATR kinase in the DNA damage response.Formula:C81H132N22O25Peso molecolare:1812.9734CA-M11
CA-M11 (compound CA-M11) is capable of entering the liver's bile salt transport system to release Mirin.Formula:C34H46N2O6SColore e forma:SolidPeso molecolare:610.80Berzosertib
CAS:Berzosertib (VE-822) is an ATR inhibitor (Ki<0.2 nM) that also inhibits ATM (Ki=34 nM). Berzosertib has antitumor activity. Cost-effective and quality-assured.Formula:C24H25N5O3SPurezza:97.34% - >99.99%Colore e forma:SolidPeso molecolare:463.55Hexapeptide-11
CAS:Hexapeptide-11 is a novel proteostasis network modulator in human diploid fibroblasts.Formula:C36H48N6O7Purezza:98%Colore e forma:SolidPeso molecolare:676.8Abd110
CAS:Abd110 (compound 42i), a Lenalidomide-based PROTAC ATR kinase degrader, selectively reduces levels of ATR and phospho-ATR while not impacting the related kinases ATM and DNA-PKcs [1].Formula:C41H42N8O7SColore e forma:SolidPeso molecolare:790.89ATM Inhibitor-8
ATM Inhibitor-8 (Compound 10r) is a potent, selective, and orally active inhibitor of ATM, exhibiting anti-tumor activity [1], characterized by an IC50 value ofFormula:C26H34N6O2Purezza:98%Colore e forma:SolidPeso molecolare:462.59ATM Inhibitor-9
ATM Inhibitor-9 (Compd 7a) is a potent inhibitor of ATM kinase, exhibiting an IC50 value of 5 nM, and is utilized in cancer research [1].Formula:C25H32N6O2Purezza:98%Colore e forma:SolidPeso molecolare:448.56Gartisertib-d8
CAS:Gartisertib-d8 (VX-803-d8) is the deuterated form of Gartisertib. Gartisertib (VX-803) acts as an orally active, selective ATP-competitive ATR inhibitor, with a Ki of less than 150 pM. It effectively inhibits ATR-driven phosphorylation of checkpoint kinase-1 (Chk1), with an IC50 value of 8 nM, and exhibits antitumor activity.Formula:C25H29F2N9O3Peso molecolare:549.61ATR-IN-30
CAS:ATR-IN-30 is a specific ATR ligand utilized in the creation of ATR PROTACs, including PROTAC ATR degrader-2.Formula:C27H30N6O4Peso molecolare:502.56ICT10336
ICT10336 is a hypoxia-reactive prodrug of the ATR inhibitor AZD6738. It specifically activates under hypoxic conditions in vitro, selectively releasing AZD6738. This action inhibits ATR activation at the T1989 and S428 phosphorylation sites, consequently disrupting HIF1a-mediated adaptation of hypoxic cancer cells and inducing cell death in both 2D and 3D cancer models. ICT10336 is also a metabolic substrate of CYPOR activity.Formula:C32H40N10O7SColore e forma:SolidPeso molecolare:708.28021GJ071 oxalate
CAS:GJ071 oxalate is a Nonsense suppressor that induces readthrough by inserting amino acids at premature termination codons.Formula:C20H29N3O7SPurezza:99.93%Colore e forma:White SolidPeso molecolare:455.525ATR-IN-9
CAS:ATR-IN-9 from patent WO2020087170A1 is a potent ATR kinase inhibitor with an IC50 of 10 nM.Formula:C22H27N7O2Colore e forma:SolidPeso molecolare:421.505GJ103 sodium salt
CAS:GJ103 sodium salt, a GJ072 analog, lowers surface tension, viscosity, and pH in aqueous solutions, aiding molecular movement.Formula:C16H13N4NaO3SPurezza:99.70% - 99.91%Colore e forma:Orange SolidPeso molecolare:364.354PIK-93
CAS:PIK-93 is the first potent, synthetic PI4K inhibitor with IC50 of 19 nM; inhibits PI3Kα with IC50 of 39 nM.Formula:C14H16ClN3O4S2Purezza:97.72%Colore e forma:SolidPeso molecolare:389.878KU-55933
CAS:KU-55933 (ATM Kinase Inhibitor) is an ATM inhibitor that is selective and ATP-competitive. KU-55933 has antitumor effects. Cost-effective and quality-assured.Formula:C21H17NO3S2Purezza:97.21% - >99.99%Colore e forma:Yellow SolidPeso molecolare:395.49
