Spirapril
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Systematic (IUPAC) name | |
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(8S)-7-[(2S)-2-{[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino}propanoyl]-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic acid | |
Clinical data | |
AHFS/Drugs.com | International Drug Names |
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Oral | |
Pharmacokinetic data | |
Bioavailability | 50% |
Metabolism | converted to spiraprilat |
Half-life | 30 to 35 hours |
Excretion | Hepatic and renal |
Identifiers | |
83647-97-6 ![]() | |
C09AA11 | |
PubChem | CID 5311447 |
DrugBank |
DB01348 ![]() |
ChemSpider |
4470933 ![]() |
UNII |
96U2K78I3V ![]() |
KEGG |
D08529 ![]() |
ChEMBL |
CHEMBL431 ![]() |
Chemical data | |
Formula | C22H30N2O5S2 |
466.616 g/mol | |
SMILES
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Spirapril hydrochloride (Renormax) is an ACE inhibitor antihypertensive drug used to treat hypertension. It belongs to dicarboxy group of ace inhibitor.
Like many ACE inhibitors, this prodrug is converted to the active metabolite spiraprilat following oral administration. Unlike other members of the group, it is eliminated both by renal and hepatic routes, which may allow for greater use in patients with renal impairment.[1] However, data on its effect upon the renal function are conflicting.[2]
References
- ↑ Shohat J, Wittenberg C, Erman A, Rosenfeld J, Boner G (1999). "Acute and chronic effects of spirapril, alone or in combination with isradipine on kidney function and blood pressure in patients with reduced kidney function and hypertension.". Scand J Urol Nephrol 33 (1): 57–62. doi:10.1080/003655999750016294. PMID 10100366.
- ↑ Noble S, Sorkin E (1995). "Spirapril. A preliminary review of its pharmacology and therapeutic efficacy in the treatment of hypertension.". Drugs 49 (5): 750–66. doi:10.2165/00003495-199549050-00008. PMID 7601014.
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