Rucaparib-d3
Rucaparib-d3 (AG014699-d3) is the deuterated -labeled Rucaparib (HY-10617A). Rucaparib (AG014699) is an orally active, potent inhibitor of PARP proteins (PARP-1, PARP-2 and PARP-3) with a Ki of 1.4 nM for PARP1. Rucaparib is a modest hexose-6-phosphate dehydrogenase (H6PD) inhibitor. Rucaparib has the potential for castration-resistant prostate cancer (CRPC) research.
For research use only. We do not sell to patients.
- CAS No.: 2271225-13-7
- Formula: C19H15D3FN3O
- Molecular Weight:326.38
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Female CD-1 nude mice aged 10-12 weeks with Capan-1 cells[2]
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Dosage:10 mg/kg for i.p. or 50, 150 mg/kg for p.o.
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Administration:IP or PO
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Result:Significantly inhibited the growth of the tumor.
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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CAS No. 2271225-13-7
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Unlabeled Cas 283173-50-2
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Molecular Weight 326.38
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Formula C19H15D3FN3O
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SMILES
O=C1C2=C3C(CCN1)=C(C4=CC=C(C=C4)CNC([2H])([2H])[2H])NC3=CC(F)=C2
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Synonyms
AG014699-d3; PF-01367338-d3
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)