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S83483

AHU-377

源叶(MedMol) 99%
  • 英文名:
  • AHU-377
  • 别名:
  • 沙库必曲; 4-(((2S,4R)-1-([1,1'-联苯]-4-基)-5-乙氧基-4-甲基-5-氧代丙烷-2-基)氨基)-4-氧代丁酸;;4-[[(2S,4R)-5-ethoxy-4-methyl-5-oxo-1-(4-phenylphenyl)pentan-2-yl]amino]-4-oxobutanoic acid; AHU-377; ENTRESTO; 4-(((2S,4R)-1-([1,
  • CAS号:
  • 149709-62-6
  • 分子式:
  • C24H29NO5
  • 分子量:
  • 411.4908
  • 核磁/质谱:
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源叶(MedMol) S83483-5mg 99% ¥425.00元 >10 - - - EA 加入购物车
源叶(MedMol) S83483-10mg 99% ¥637.50元 >10 - - - EA 加入购物车
源叶(MedMol) S83483-50mg 99% ¥1490.00元 >10 - - - EA 加入购物车
源叶(MedMol) S83483-250mg 99% ¥5100.00元 >10 - - - EA 加入购物车
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相关产品

  • 提示:详情请下载说明书。
  • 产品描述: Sacubitril (AHU-377) is a potent and orally active NEP (neprilysin) inhibitor with an IC50 of 5 nM. Sacubitril is a component of the heart failure medicine LCZ696. Sacubitril can be used for the research of heart failure, hypertension and COVID-19
  • 靶点: IC50: 5 nM (NEP);Neprilysin
  • 体外研究:
    Sacubitril (AHU-377) is a single molecule that is comprised of molecular moieties of valsartan, an ARB, and Sacubitril (AHU-377), a neprilysin inhibitor (1:1 ratio). Sacubitril (AHU-377) is converted by enzymatic cleavage of the ethyl ester into the active neprilysin inhibiting metabolite LBQ657. The inactive NEPi precursor, Sacubitril (AHU-377), does not inhibit collagen accumulation in fibroblasts nor cardiac myocyte hypertrophy. In cardiac fibroblasts, the active NEPi LBQ657 had no discernible effects. In contrast, LBQ657 modestly inhibits cardiac myocyte hypertrophy
  • 体内研究:
    In vehicle-treated dogs, ANF increases urinary sodium excretion from 17.3±3.6 to 199.5±18.4 pequivkglmin. This effect is potentiated significantly in animals which receive Sacubitril (AHU-377). Urinary volume is also potentiated in animals which receive an iv administration of Sacubitril (AHU-377). In normotensive rats, pretreatment with Sacubitril (3, 10 and 30 mg/kg, PO.) augments ANP-evoked plasma cGMP levels by 2.4, 3.3 and 4.0 fold, respectively (4h AUC compared to vehicle). Sacubitril (30 and 100 mg/kg, PO) produces a dose-dependent antihypertensive effect in Dahl-SS rats
  • 参考文献:
    1. Ksander GM, et al. Dicarboxylic acid dipeptide neutral endopeptidase inhibitors. J Med Chem. 1995 May 12;38(10):1689-700. 2. Voors AA, et al. The potential role of valsartan + AHU377 ( LCZ696 ) in the treatment of heart failure. Expert Opin Investig Drugs. 2013 Aug;22(8):1041-7. 3. von Lueder TG, et al. Angiotensin receptor neprilysin inhibitor LCZ696 attenuates cardiac remodeling and dysfunction after myocardial infarction by reducing cardiac fibrosis and hypertrophy. Circ Heart Fail. 2015 Jan;8(1):71-8. 4. Hegde, L.G., et al. Comparative efficacy of AHU-377, a potent neprilysin inhibitor, in two rat models of volume-dependent hypertension. BMC Pharmacol 11, P33 (2011).
  • 溶解性: Soluble  in  DMSO、H2O
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.43 ml 12.151 ml 24.302 ml
    5 mM 0.486 ml 2.43 ml 4.86 ml
    10 mM 0.243 ml 1.215 ml 2.43 ml
    50 mM 0.049 ml 0.243 ml 0.486 ml
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