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Pronunciation | /ruːˈkæpərɪb/ roo-KAP-ər-ib |
Trade names | Rubraca |
Other names | CO-338, AG-014699, PF-0136738, PF-01367338 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a617002 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | 30–45% (Tmax = 1.9 hours) |
Protein binding | 70% (in vitro) |
Metabolism | Liver (primarily CYP2D6; 1A2 and 3A4 to a lesser extent) |
Elimination half-life | 17–19 hours[2] |
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ECHA InfoCard | 100.247.490 |
Chemical and physical data | |
Formula | C19H18FN3O |
Molar mass | 323.371 g·mol−1 |
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Rucaparib, sold under the brand name Rubraca, is a PARP inhibitor used as an anti-cancer agent.[2] Rucaparib is a first-in-class pharmaceutical drug targeting the DNA repair enzyme poly-ADP ribose polymerase-1 (PARP-1). It is taken by mouth.[2][4]
The most common side effects include tiredness or weakness, nausea (feeling sick), increased levels of creatinine (which may indicate kidney problems) and liver enzymes in the blood (which may indicate liver damage), vomiting, anaemia (low red blood cell counts), decreased appetite, dysgeusia (taste disturbances), diarrhoea, thrombocytopenia (low levels of platelets) and abdominal pain (belly ache).[3][2]
Rubraca EPAR
was invoked but never defined (see the help page).