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Cat. No. Product Name Information
PC-42831

KU-55933

ATM inhibitor

KU-55933 (KU55933) is a potent, specific, ATP-competitive inhibitor of ATM with Ki/IC50 of 2.2/13 nM, >100-fold selectivity against other members of the PIKK family kinases.
PC-62548

GSK635416A

ATM inhibitor

GSK 635416A is a novel ATM inhibitor with highly selective radiosensitizing activity, inhibits radiation induced phosphorylation of ATM.
PC-61826

AZD1390

ATM inhibitor

AZD1390 (AZD-1390) is a novel potent, selective, orally available and CNS penetrant ATM inhibitor with IC50 of 0.78 nM, displays >1,000-fold selectivity over closely related (PIKKs) and distant kinases.
PC-70146

BAY-1895344 hydrochloride

ATR inhibitor

BAY-1895344 (Elimusertib) hydrochloride is a potent, selective, orally active ATR inhibitor with low-nanomolar potency (IC50=7 nM).
PC-70111

ATM inhibitor AZ31

ATM inhibitor

AZ31 is a potent, highly selective and orally active ATM inhibitor with enzyme IC50 of <1.2 nM, cell IC50 of 46 nM.
PC-70110

CBP-93872

G2 checkpoint inhibitor

CBP-93872 is a potent G2 checkpoint inhibitor that specifically abrogates the DNA double-stranded break (DSB)-induced G2 checkpoint, inhibits NBS1-mediated ATR activation.
PC-60277

BAY 1895344

ATR inhibitor

BAY 1895344 (BAY-1895344, Elimusertib) is a novel potent, highly selective ATR kinase inhibitor with IC50 of 7.0 nM.
PC-44042

VE-821

ATR inhibitor

VE-821 (VE821) is a potent, selective and ATP-competitive inhibitor of ATR with Ki/IC50 of 13 nM/26 nM, respectively.
PC-42030

AZD0156

ATM inhibitor

AZD0156 (AZD-0156) is a potent, highly selective and orally bioavailable ATM kinase inhibitor with IC50 of 0.58 nM.
PC-45607

AZD6738

ATR inhibitor

AZD6738 (Ceralasertib) is a potent and selective inhibitor of ATR with IC50 of 1 nM.
PC-42778

CP-466722

ATM inhibitor

CP-466722 is a poten and selective ATM inhibitor (IC50=0.41 uM) without effect on ATR kinase, does not inhibit PI3K, PI3K-like protein kinases or Abl kinase.
PC-42333

GJ103 sodium salt

Read-through compound

GJ103 sodium salt is a novel small molecular read-through (SMRT) compound that can induce read through of nonsense mutations in the ATM gene.

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