Fosinopril
| Systematic (IUPAC) name | |
|---|---|
| (2S,4S)-4-cyclohexyl-1-(2-{[2-methyl-1-(propanoyloxy)propoxy](4-phenylbutyl)phosphoryl}acetyl)pyrrolidine-2-carboxylic acid | |
| Clinical data | |
| Trade names | Monopril |
| AHFS/Drugs.com | monograph |
| MedlinePlus | a692020 |
| Pregnancy cat. | D (AU) |
| Legal status | ℞ Prescription only |
| Routes | oral |
| Pharmacokinetic data | |
| Bioavailability | ~36% |
| Protein binding | 87% (fosinoprilat) |
| Metabolism | hepatic, GIT mucosa (to fosinoprilat) |
| Half-life | 12 hours (fosinoprilat) |
| Excretion | renal |
| Identifiers | |
| CAS number | 98048-97-6 |
| ATC code | C09AA09 |
| PubChem | CID 55891 |
| DrugBank | APRD00526 |
| ChemSpider | 10482016 |
| UNII | R43D2573WO |
| KEGG | D07992 |
| ChEMBL | CHEMBL1201310 |
| Chemical data | |
| Formula | C30H46NO7P |
| Mol. mass | 563.663 g/mol |
| SMILES | eMolecules & PubChem |
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Fosinopril is an angiotensin converting enzyme (ACE) inhibitor[1] used for the treatment of hypertension and some types of chronic heart failure. Fosinopril is the only phosphinate-containing ACE inhibitor marketed. It is marketed by Bristol-Myers Squibb under the trade name Monopril.
[edit] Fosinoprilat and Fosinopril
Fosinoprilat proved to have the same problem as enalaprilat and the other carboxylate-containing ACE inhibitors (namely poor oral bioavailability). Addition of a hydrophobic side-chain modulated the ionisation characteristics of the molecule making it more bioavailable. Fosinopril is administered as a prodrug and is converted in vivo to the active form fosinoprilat.
[edit] References
- ^ Pilote L, Abrahamowicz M, Eisenberg M, Humphries K, Behlouli H, Tu JV (May 2008). "Effect of different angiotensin-converting-enzyme inhibitors on mortality among elderly patients with congestive heart failure". CMAJ 178 (10): 1303–11. doi:10.1503/cmaj.060068. PMC 2335176. PMID 18458262. http://www.cmaj.ca/cgi/pmidlookup?view=long&pmid=18458262.
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