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Rabusertib (LY2603618) is an effective and selective Chk1 inhibitor with an IC50 of 7 nM.
Invest New Drugs. 2025 Jan 27.
Synergistic antitumor effect of MK-1775 and CUDC-907 against prostate cancer
Rabusertib (LY2603618) purchased from AbMole
| Molecular Weight | 436.3 |
| Formula | C18H22BrN5O3 |
| CAS Number | 911222-45-2 |
| Solubility (25°C) | DMSO 12 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
| Related Checkpoint Products |
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| AZD7762
AZD7762 is a potent ATP-competitive checkpoint kinase inhibitor with an IC50 of 5 and <10 nM for CHK1 and CHK2 respectively. |
| BIBR1532
BIBR1532 is a potent and selective telomerase inhibitor with IC50 of 100 nM. BIBR 1532 inhibits the proliferation of JVM13 leukemia cells with an IC50 of 52 μM, and similar effect also occurs in other leukemia cell lines such as Nalm-1, HL-60, and Jurkat. BIBR1532 is also an inhibitor of TERT, the rate-limiting enzyme in the regulation of telomerase activity. |
| PF-477736
PF-477736 is a selective checkpoint kinase 1 (Chk1) inhibitor with Ki values of 0.49 nM and 47 nM for CHK1 and CHK2 respectively. |
| SCH 900776
SCH 900776 (MK-8776) is a highly potent and functionally selective CHK1 inhibitor with IC50 of 3 nM. |
| CHIR-124
CHIR-124 is a novel and potent Chk1 inhibitor with IC50 of 0.3 nM. |
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