AZD2171
File:AZD2171.svg | |
Clinical data | |
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Routes of administration | Oral |
Pharmacokinetic data | |
Elimination half-life | 12 to 35 hours |
Identifiers | |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C25H27FN4O3 |
Molar mass | 450.5 g/mol |
WikiDoc Resources for AZD2171 |
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Most recent articles on AZD2171 |
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Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on AZD2171 at Clinical Trials.gov Clinical Trials on AZD2171 at Google
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US National Guidelines Clearinghouse on AZD2171
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Patient Resources / Community |
Directions to Hospitals Treating AZD2171 Risk calculators and risk factors for AZD2171
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Causes & Risk Factors for AZD2171 |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Overview
AZD2171 (tentative trade name Recentin) is a potent inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinases. It is being developed by AstraZeneca as a possible chemotherapeutic agent for oral administration.
As of 2007, it is undergoing Phase I clinical trials for the treatment of non-small cell lung cancer and colorectal cancer in adults, as well as tumors of the central nervous system in children.
Further reading
- Wedge S, Kendrew J, Hennequin L; et al. (2005). "AZD2171: a highly potent, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for the treatment of cancer". Cancer Res. 65 (10): 4389–400. PMID 15899831.
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- Tyrosine kinase inhibitors