Pazopanib
From Self-sufficiency
File:Pazopanib structure.svg | |
Systematic (IUPAC) name | |
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5-[[4-[(2,3-Dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methylbenzolsulfonamide | |
Clinical data | |
[[Regulation of therapeutic goods |Template:Engvar data]] | |
Pregnancy category |
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Routes of administration | Oral |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Protein binding | >99% |
Metabolism | Hepatic (CYP3A4, 1A2 and 2C8-mediated) |
Biological half-life | 31 hours (mean) |
Excretion | Mostly fecal |
Identifiers | |
CAS Number | 444731-52-6 |
ATC code | L01XE11 (WHO) |
PubChem | CID 11525740 |
ChemSpider | 8289501 |
Chemical data | |
Formula | C21H23N7O2S |
Molar mass | 437.517 g/mol[[Script error: No such module "String".]] |
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Pazopanib (trade name Votrient) is a potent and selective multi-targeted receptor tyrosine kinase inhibitor of VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-a/β, and c-kit that blocks tumor growth and inhibits angiogenesis. It has been approved for renal cell carcinoma by the U.S. Food and Drug Administration.[1] Pazopanib may also be active in ovarian cancer[2] and soft tissue sarcoma.[3] Pazopanib also appears effective in the treatment of non-small cell lung carcinoma.[2]
References
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- ↑ "FDA Approves GlaxoSmithKline's Votrient(TM) For Advanced Renal Cell Cancer". Medical News Today. 20 October 2009. Retrieved 8 June 2010.
- ↑ 2.0 2.1 "Pazopanib shows encouraging activity in several tumour types, including soft tissue sarcoma and ovarian cancer". FierceBiotech. 2008-09-15. Retrieved 2010-08-10.
- ↑ Sleijfer, S.; Ray-Coquard, I.; Papai, Z.; Le Cesne, A.; Scurr, M.; Schoffski, P.; Collin, F.; Pandite, L.; Marreaud, S. (2009). "Pazopanib, a Multikinase Angiogenesis Inhibitor, in Patients with Relapsed or Refractory Advanced Soft Tissue Sarcoma: A Phase II Study from the European Organisation for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC Study 62043)". Journal of Clinical Oncology. 27 (19): 3126. doi:10.1200/JCO.2008.21.3223. PMID 19451427.
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