Clinical data | |
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Trade names | Xalkori, others |
Other names | PF-02341066 1066 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a612018 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | 43% |
Protein binding | 91% |
Metabolism | Liver (CYP3A4/CYP3A5-mediated) |
Elimination half-life | 42 hours |
Excretion | Faeces (63%), urine (22%) |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.166.440 |
Chemical and physical data | |
Formula | C21H22Cl2FN5O |
Molar mass | 450.34 g·mol−1 |
3D model (JSmol) | |
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(what is this?) (verify) |
Crizotinib, sold under the brand name Xalkori among others, is an anti-cancer medication used for the treatment of non-small cell lung carcinoma (NSCLC).[2][3][4][5] Crizotinib inhibits the c-Met/Hepatocyte growth factor receptor (HGFR) tyrosine kinase, which is involved in the oncogenesis of a number of other histological forms of malignant neoplasms.[6] It also acts as an ALK (anaplastic lymphoma kinase) and ROS1 (c-ros oncogene 1) inhibitor.[7][8][9]
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: CS1 maint: DOI inactive as of November 2024 (link)