Pivopril
- Product Name
- Pivopril
- CAS No.
- 81045-50-3
- Chemical Name
- Pivopril
- Synonyms
- Pivopril;RHC 3659(S);N-Cyclopentyl-N-[(S)-3-[(2,2-dimethyl-1-oxopropyl)thio]-2-methyl-1-oxopropyl]glycine;Glycine, N-cyclopentyl-N-[(2S)-3-[(2,2-dimethyl-1-oxopropyl)thio]-2-methyl-1-oxopropyl]-
- CBNumber
- CB21116119
- Molecular Formula
- C16H27NO4S
- Formula Weight
- 329.45
- MOL File
- 81045-50-3.mol
Pivopril Property
- Boiling point:
- 490.4±38.0 °C(Predicted)
- Density
- 1.16±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- form
- Solid
- pka
- 3.49±0.10(Predicted)
- color
- White to off-white
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- API0012294
- Product name
- PIVOPRIL
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.47
- Updated
- 2021/12/16
- Product number
- CSN21805
- Product name
- Pivopril
- Packaging
- 1mg
- Price
- $592
- Updated
- 2021/12/16
- Product number
- CSN21805
- Product name
- Pivopril
- Packaging
- 5mg
- Price
- $1173
- Updated
- 2021/12/16
- Product number
- CSN21805
- Product name
- Pivopril
- Packaging
- 10mg
- Price
- $1999
- Updated
- 2021/12/16
- Product number
- CSN21805
- Product name
- Pivopril
- Packaging
- 25mg
- Price
- $3519
- Updated
- 2021/12/16
Pivopril Chemical Properties,Usage,Production
Uses
Antihypertensive.
Definition
ChEBI: Pivopril is a N-acyl-amino acid.
in vivo
Pivalopril is a new compound with a hindered sulfur group that has been compared to Captopril for oral angiotensin-converting enzyme (ACE) inhibition in rats and dogs and antihypertensive activity in rats. In separate groups of conscious normotensive rats, Pivalopril (0.03-1.0 mg/kg, orally [p.o.]) produces a dose-related antagonism of angiotensin I (AngI)-induced pressor effects. The ED50 for Pivalopril and Captopril is 0.1 mg/kg. In conscious normotensive dogs, Pivalopril (incremental doses of 0.01-1.0 mg/kg, p.o.) produces a dose-related antagonism of AngI pressor effects. The ED50 is 0.17 mg/kg for Pivalopril and 0.06 mg/kg for Captopril. At equieffective doses the two compounds have similar durations of action. In sodium-deficient, conscious spontaneously hypertensive rats (SHR), Pivalopril (1-100 mg/kg, p.o.) produces a dose-related reduction in mean arterial pressure. The potency and duration are similar to those of Captopril. In the sodium-replete SHR, 5 days of oral dosing with Pivalopril (100 mg/kg per day) decreases mean arterial pressure more effectively than Captopril (100 mg/kg per day). It is concluded that Pivalopril is a potent, orally effective ACE inhibitor and antihypertensive agent[2].
Pivopril Preparation Products And Raw materials
Raw materials
Preparation Products
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