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ChemicalBook--->CAS DataBase List--->83647-97-6

83647-97-6

83647-97-6 Structure

83647-97-6 Structure
IdentificationBack Directory
[Name]

Spirapril
[CAS]

83647-97-6
[Synonyms]

SPIRAPRIL
Sandopfil
Sch-33844
Espirapril
Brn 4277924
Spiraprilum
Spiraprilic acid
Spiraprilum [latin]
Spirapril [inn:ban]
Espirapril [spanish]
SPIRAPRIL FOR SYSTEM SUITABILITY EPY
SPIRAPRIL FOR SYSTEM SUITABILITY EPY(CRM STANDARD)
(8S-(7(R*(R*)),8R*))-7-(2-((1-(Ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic acid
1,4-Dithia-7-azaspiro(4,4)nonane-8-carboxylic acid, 7-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)-, (8S-(7(R*(R*)),8R*))-
[Molecular Formula]

C22H30N2O5S2
[MDL Number]

MFCD00865789
[MOL File]

83647-97-6.mol
[Molecular Weight]

466.61
Chemical PropertiesBack Directory
[Boiling point ]

697.8±55.0 °C(Predicted)
[density ]

1.32±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

2.99±0.20(Predicted)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

p-Toluenesulfonic acid-->1,2-Ethanedithiol-->Ethyl 2-oxo-4-phenylbutyrate
Hazard InformationBack Directory
[Uses]

Spirapril is an Angiotensin-converting enzyme inhibitor and used to treat high blood pressure.
[Definition]

ChEBI: Spirapril is a dipeptide, a dithioketal, an azaspiro compound, a dicarboxylic acid monoester, an ethyl ester, a tertiary carboxamide, a secondary amino compound and a pyrrolidinecarboxylic acid. It has a role as a prodrug, an EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor and an antihypertensive agent. It is functionally related to a spiraprilat.
[in vivo]

Spirapril (feeding needle; 10 mg/kg; 3 weeks) decreases alcohol intake in TGM123 mice and dose not reduce the alcohol consumption in TLM mice[2].
Spirapril shows a 40.2% reduction in ACE activity in brain membrane from treated-mice[2].
Spirapril can crosses the blood-brain barrier and suppresses the transgene effect in the experiments[2].
Spirapril prevents left ventricular hypertrophy, decreases myocardial damage and promotes angiogenesis in spontaneously hypertensive rats[3].

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