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| CAS_number_Ref = {{cascite|correct|??}} | |||
| CAS_number = 118949-22-7 | | CAS_number = 118949-22-7 | ||
| ATC_prefix = L02 | | ATC_prefix = L02 |
Revision as of 02:58, 24 October 2011
Pharmaceutical compoundClinical data | |
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ATC code | |
Pharmacokinetic data | |
Bioavailability | Very high |
Metabolism | Hepatic |
Elimination half-life | 8 hours |
Identifiers | |
IUPAC name
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CAS Number | |
PubChem CID | |
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KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C16H13ClN6 |
Molar mass | 324.768 g/mol g·mol |
3D model (JSmol) | |
SMILES
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InChI
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Vorozole is an imidazole based competitive inhibitor of the aromatase enzyme. It underwent clinical testing for evaluation for use as an antineoplastic agent; however it was withdrawn from testing when no difference was detected in the duration of median survival as compared to the progestational agent megestrol acetate and research instead focused on the other third generation aromatase inhibitors anastrozole, letrozole and exemestane.
It is selective.
Chemistry
Prous, J.; Grant, J.; Castaner, J.; Drugs Future 1994, 457.
References
- Goss PE (1998). "Pre-clinical and clinical review of vorozole, a new third generation aromatase inhibitor" (PDF). Breast Cancer Res. Treat. 49. Suppl 1: S59–65, discussion S73–7. PMID 9797019.
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