ZofenoprilCalcium , 98% , 81938-43-4
Synonym(s):
(4S)-1-[(2S)-3-(benzoylthio)-2-methyl-1-oxopropyl]-4-(phenylthio)-L-proline calcium salt
CAS NO.：81938-43-4
Empirical Formula: C44H44CaN2O8S4
Molecular Weight: 897.167
MDL number: MFCD08704648
| Pack Size | Price | Stock | Quantity |
| 250mg | RMB216.80 | In Stock |
|
| 1g | RMB471.20 | In Stock |
|
| others | Enquire |
PRODUCT Properties
| Melting point: | >250°C |
| alpha | D23 -67.6° (c = 1 in methanol/HCl) |
| storage temp. | Inert atmosphere,2-8°C |
| solubility | DMSO: >5mg/mL |
| form | powder |
| color | white to off-white |
Description and Uses
Zofenopril is a prodrug form of the angiotensin-converting enzyme (ACE) inhibitor zofenoprilat. Zofenopril is hydrolyzed by cardiac esterases in vivo to form zofenoprilat. It inhibits ACE with an IC50 value of 0.9 nM in heart tissue homogenates and inhibits cardiac ACE activity in isolated perfused rat hearts. It reduces mean arterial blood pressure in two kidney-one clip renal hypertensive (2K-1C) rats and spontaneously hypertensive rats (SHRs) when administered at doses of 2.2, 6.6, and 22 mg/kg. Unlike the ACE inhibitor ramipril , zofenopril does not affect bronchoalveolar lavage fluid (BALF) levels of bradykinin or prostaglandin E2 (PGE2; ) or increase coughing induced by citric acid in guinea pigs.
Angiotensin-converting enzyme ACE inhibitor. A prodrug that is de-esterified to the active inhibitor, the sulfhydryl group containing metabolite, Zofenoprilat
