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
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2MG 428 Get Quote
5MG 628 Get Quote
10MG 897 Get Quote
25MG 1332 Get Quote
50MG 1791 Get Quote
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Biological Information

  • Product Name
    Temocaprilat
  • Note
    Research use only, not for human use.
  • Brief Description
    Temocaprilat is an Angiotensin-converting Enzyme (ACE) inhibitor.
  • Description
    Temocaprilat 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 Vivo
    Animal 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.
  • Synonyms
    RS-5139 | RS 5139 | RS5139 | RNH 5139 | RNH-5139 | RNH5139
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    ACE
  • Recptor
    Immunology/Inflammation related
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    110221-53-9
  • Formula Weight
    448.55
  • Molecular Formula
    C21H24N2O5S2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    OC(=O)CN1C[C@H](SC[C@H](NC(CCc2ccccc2)C(O)=O)C1=O)c1cccs1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With 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.
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