Temocaprilat
CAS No. 110221-53-9
Temocaprilat( RS-5139 | RS 5139 | RS5139 | RNH 5139 | RNH-5139 | RNH5139 )
Catalog No. M27310 CAS No. 110221-53-9
Temocaprilat is an Angiotensin-converting Enzyme (ACE) inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 428 | Get Quote |
|
| 5MG | 628 | Get Quote |
|
| 10MG | 897 | Get Quote |
|
| 25MG | 1332 | Get Quote |
|
| 50MG | 1791 | Get Quote |
|
| 100MG | 2421 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameTemocaprilat
-
NoteResearch use only, not for human use.
-
Brief DescriptionTemocaprilat is an Angiotensin-converting Enzyme (ACE) inhibitor.
-
DescriptionTemocaprilat is an Angiotensin-converting Enzyme (ACE) inhibitor. Temocaprilat is effectively excreted in bile via cMOAT that is deficient in EHBR and that many of other ACE inhibitors have low affinity for cMOAT.(In Vivo):Biliary clearance of Temocaprilat after i.v. administration of [14C]temocapril x HCl (1.0 mg/kg) in EHBR was significantly lower than that in Sprague-Dawley rats (5.00 ml/min/kg for Sprague-Dawley rats vs. 0.25 ml/min/kg for EHBR). The uptake of Temocaprilat into canalicular membrane vesicles (CMVs) prepared from Sprague-Dawley rats was stimulated in the presence of ATP, whereas little stimulation was observed in CMVs from EHBR. The initial uptake rate of ATP-dependent transport of Temocaprilat showed saturation kinetics; we obtained an apparent V(max) value of 1.14 nmol/min/mg protein and a K(m) value 92.5 microM. ATP-dependent transport of Temocaprilat was competitively inhibited by 2,4-dinitrophenyl-S-glutathione, a typical substrate for cMOAT with an inhibition constant (K(i)) of 25.8 microM. The K(m) value for the uptake of 2,4-dinitrophenyl-S-glutathione into CMVs (K(m) = 29.6 microM) was consistent with this K(i) value. In addition, the ATP-dependent uptake of 2,4-dinitrophenyl-S-glutathione was inhibited by Temocaprilat in a concentration-dependent manner. Active forms of some ACE inhibitors (benazepril, cilazapril, delapril, enalapril and imidapril) did not affect the transport of Temocaprilat into CMVs even at concentrations as high as 200 microM.
-
In Vitro——
-
In VivoAnimal Model:Six 10-week-old WKYs and SHRs and six 50-week-old (aging control) SHRs.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.
-
SynonymsRS-5139 | RS 5139 | RS5139 | RNH 5139 | RNH-5139 | RNH5139
-
PathwayMetabolic Enzyme/Protease
-
TargetACE
-
RecptorImmunology/Inflammation related
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number110221-53-9
-
Formula Weight448.55
-
Molecular FormulaC21H24N2O5S2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOC(=O)CN1C[C@H](SC[C@H](NC(CCc2ccccc2)C(O)=O)C1=O)c1cccs1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Piwinski J J , Shih N Y , Billah M M . Chapter 7. Recent Approaches Towards Inhibiting Allergic Eosinophilia[J]. Annual reports in medicinal chemistry, 1999, 34(08):61-70.
molnova catalog
related products
-
Rentiapril racemate
Rentiapril racemate (SA-446 racemate) is the racemic form of Rentiapril, exhibiting anti-inflammatory properties and potential applications in glaucoma research.
-
Abz-FR-K(Dnp)-P-OH
Excellent angiotensin I-converting enzyme (ACE) substrate with a Km value of 4.0 μM and a kcat value of 210s-1.
-
H-Ile-Pro-Pro-OH
H-Ile-Pro-Pro-OH, a milk-derived peptide, inhibits angiotensin-converting enzyme (ACE) with an IC50 of 5 μM.
Cart
sales@molnova.com