
Temocaprilat
CAS No. 110221-53-9
Temocaprilat ( RS-5139 | RS 5139 | RS5139 | RNH 5139 | RNH-5139 | RNH5139 )
产品货号. M27310 CAS No. 110221-53-9
Temocaprilat 是一种血管紧张素转换酶 (ACE) 抑制剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥3856 | 有现货 |
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5MG | ¥5654 | 有现货 |
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10MG | ¥8076 | 有现货 |
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25MG | ¥11988 | 有现货 |
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50MG | ¥16119 | 有现货 |
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100MG | ¥21789 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Temocaprilat
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Temocaprilat 是一种血管紧张素转换酶 (ACE) 抑制剂。
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产品描述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.
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体外实验——
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体内实验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.
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同义词RS-5139 | RS 5139 | RS5139 | RNH 5139 | RNH-5139 | RNH5139
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通路Metabolic Enzyme/Protease
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靶点ACE
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受体Immunology/Inflammation related
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研究领域——
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适应症——
化学信息
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CAS Number110221-53-9
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分子量448.55
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分子式C21H24N2O5S2
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纯度>98% (HPLC)
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溶解度——
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SMILESOC(=O)CN1C[C@H](SC[C@H](NC(CCc2ccccc2)C(O)=O)C1=O)c1cccs1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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.
产品手册




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