ChemicalBook--->CAS DataBase List--->110221-53-9

110221-53-9

110221-53-9 Structure

110221-53-9 Structure
IdentificationBack Directory
[Name]

Temocaprilat
[CAS]

110221-53-9
[Synonyms]

RS-5139
Temocaprilat
Temocaprilate
Temocapril Diacid
TEMOCAPRILAT(FORR&DONLY)
[[[2S,6R]-6-[[(S)-1-Carboxy-3-phenylpropyl]amino]hexahydro-5-oxo-2-(2-thienyl)-1,4-thiazepin]-4-yl]acetic acid
(2S,6R)-6-[[(1S)-1-Carboxy-3-phenylpropyl]amino]tetrahydro-5-oxo-2-(2-thienyl)-1,4-thiazepine-4(5H)-acetic Acid
(+)-[(2S,6R)-6-[[(S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-5-oxo-2-(2-thienyl)perhydro-1,4-thiazepin-4-yl]acetic acid
[Molecular Formula]

C21H24N2O5S2
[MDL Number]

MFCD00871951
[MOL File]

110221-53-9.mol
[Molecular Weight]

448.56
Chemical PropertiesBack Directory
[Appearance]

White to Off-White Solid
[Melting point ]

>2300C (dec)
[alpha ]

25D +63.4° (c = 1 in DMF)
[Boiling point ]

743.6±60.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

Hygroscopic, -20?C Freezer, Under Inert Atmosphere
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

2.09±0.10(Predicted)
[color ]

White to Off-White
Hazard InformationBack Directory
[Chemical Properties]

White to Off-White Solid
[Uses]

Antihypertensive
[Description]

Temocaprilat is an inhibitor of angiotensin-converting enzyme (ACE; IC50 = 3.6 nM for rabbit lung ACE). It inhibits contraction of isolated rat aorta induced by angiotensin I with an IC50 value of 7.6 nM. Temocaprilat (1-30 μg/kg, i.v.) inhibits angiotensin I-induced pressor responses in anesthetized rats in a dose-dependent manner.
[Definition]

ChEBI: Temocaprilat is a non-proteinogenic alpha-amino acid.
[in vivo]

Temocaprilat (1 mg/kg/d; i.v.; 4 weeks) significantly reduces systolic blood pressure with time-dependent manner in spontaneously hypertensive (SHR) rats. Temocaprilat improves myocardial fibrosis and oxidative stress in Wistar-Kyoto (WKY) rats and SHR rats[3].

Animal Model:Six 10-week-old WKYs and SHRs and six 50-week-old (aging control) SHRs[3].
Dosage:1 mg/kg/d.
Administration:Intravenous injection; 4 weeks.
Result:Reduced the expression levels of myocardial fibrosis, transforming growth factor-β1 (TGF-β1) mRNA and fibroblast growth factor-2 (FGF-2) mRNA in the left ventricle (LV).
Weakened the expression levels of 8-isoprostane, p22phox mRNA, p47phox mRNA and gp91phox mRNA in LV.
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