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Product introduction
iRucaparib-AP6 is a highly efficient and specific PROTAC PARP1 degrader. iRucaparib-AP6, a non-trapping PARP1 degrader, blocks both the catalytic activity and scaffolding effects of PARP1 In Vitro iRucaparib-AP6 (0-10 μM; 24 hours) decreases PARP-1 level in a dose dependent manner, exhibits a half-maximal degrading concentration (DC 50 ) of 82 nM (D max = 92%). iRucaparib-AP6 (0-20 μM; 24 hours) induces degradation of PARP1 at low concentrations. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: Primary rat neonatal cardiomyocyte cells Concentration: 0.001 μM; 0.01 μM; 0.1 μM; 1 μM; 10 μM Incubation Time: 24 hours Result: Decreased PARP-1 level in primary rat neonatal cardiomyocyte cells. Western Blot AnalysisCell Line: Primary rat neonatal cardiomyocyte cells Concentration: 0.05 μM; 0.1 μM; 0.2 μM; 0.5 μM; 1 μM; 2 μM; 5 μM;10 μM; 20 μM Incubation Time: 24 hours Result: Induced robust PARP1 degradation at concentrations as low as 50 nM. Form:Solid IC50& Target:PARP1 82 nM (DC 50 )
Chinese name
iRucaparib-AP6
English name
iRucaparib-AP6
Chinese alias
-
English alias
-
CAS number
2410557-00-3
molecular formula
C46H55FN6O11
molecular weight
886.96 g/mol
Exact mass
≥99%
PSA
-
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iRucaparib-AP6 5mg

iRucaparib-AP6 5mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg; ≥99%.

item number:I650808-5mg
Product model:5mg
level: 5mg; ≥99%
Lead Time:30days
sold 501 Items
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5mg

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