Chemical structure
Cat.No.
Product Name
CAS no.
Target
NU6027 is a potent ATR/CDK inhibitor, inhibits CDK1/2, ATR and DNA-PK with Ki of 2.5 μM/1.3 μM, 0.4 μM and 2.2 μM, enter cells more readily than the 6-aminopurine-based inhibitors.
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor with IC50/Ki of 12.9 nM/2.2 nM in cell-free assays, and is highly selective for ATM as compared to DNA-PK, PI3K/PI4K, ATR and mTOR.
KU 59403 is a potentATMinhibitor, with IC50 values of 3nM, 9.1μM and 10μM for ATM, DNA-PK and PI3K, respectively.
CGK733 is a potentATM/ATRinhibitor, used for the research of cancer.
KU-60019 is an improvedATMkinase-specific inhibitor with IC50 of 6.3nM.
YN420066 CP-466722 1080622-86-1
CP-466722 is a rapidly reversible inhibitor ofATM, with an IC50 of 4.1μM, and has no effects on PI3K or closely related PI3K-like protein kinase (PIKK) family members.
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13 nM/26 nM in cell-free assays, shows inhibition of H2AX phosphorylation, minimal activity against PIKKs ATM, DNA-PK, mTOR and...
YN420189 Berzosertib 1232416-25-9
VE-822 is an ATR inhibitor with IC50 of 19 nM in HT29 cells.
AZ20 is a novel potent and selective inhibitor of ATR kinase with IC50 of 5 nM in a cell-free assay, 8-fold selectivity over mTOR.
YN420219 ETP-46464 1345675-02-6
ETP-46464 is a potent and selective inhibitor of ATR with IC50 of 25 nM.
YN420260 (S)-Ceralasertib 1352226-87-9
(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC50 of 2.578nM. (S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidineATRinhibitor with excellent...
YN420259 Ceralasertib 1352226-88-0
AZD6738 is an orally active, and selective ATR kinase inhibitor with IC50 of 1 nM. Phase 1/2.
YN420176 ATR inhibitor 2 1613191-99-3
VX-803 (M4344) is an ATP-competitive, orally active, and selective inhibitor of ataxia telangiectasia and Rad3 related (ATR) kinase with Ki of < 150 pM. VX-803 (M4344) potently inhibits ATR-driven phosphorylated checkpoint...
AZD0156 is a potent, selective and orally activeATMinhibitor with an IC50 of 0.58nM. AZD0156 inhibits theATM-mediated signaling, prevents DNA damage checkpoint activation, disrupts DNA damage repair, and induces tum...
AZD1390 is a first-in-class orally available and CNS penetrant ATM inhibitor with an IC50 of 0.78 nM in cells and >10,000-fold selectivity over closely related members of the PIKK family of enzymes and excellent selectivity ...
AZ32 is an orally bioavailable and blood-brain barrier-penetratingATMinhibitor with an IC50 of <6.2nM for ATM enzyme, and an IC50 of 0.31μM for ATM in cell.
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