Sacubitrilat

SKU: orb1296199

Description

Sacubitrilat

Research Area

Metabolism Research

Key Properties

• CAS Number: 149709-44-4
• MW: 383.44
• Purity: 99.89%
• Formula: C₂₂H₂₅NO₅
• SMILES: C[C@H](C[C@@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)CCC(O)=O)C(O)=O
• Target: Neprilysin
• Solubility: 10% DMSO+40% PEG300+5% Tween 80+45% Saline:4 mg/mL (10.43 mM);DMSO:100 mg/mL (260.8 mM)

Bioactivity

• In Vivo:
  Pharmacokinetics of Sacubitril, Sacubitrilat, and valsartan following the administration of single oral doses of LCZ696 400 or 1200 mg under fasting conditions are summarized. The mean plasma concentrations of Sacubitril increases rapidly with a median Tmax of 0.52 h for the 400 mg dose and 1.05 h for the 1200 mg dose, followed by Sacubitrilat, with the corresponding Tmax values of 2.07 and 3.05 h, respectively. The median Tmax for valsartan is 2.07 h for both the LCZ696 400 mg and 1200 mg doses. The Cmax of Sacubitrilat shows a dose-proportional increase, while the Cmax of Sacubitril and Valsartan shows less than proportional increases between the doses .
• In Vitro:
  Sacubitrilat is bound to the active site of NEP by an intricate network of interactions that involves all functional groups of the compound giving rise to the high inhibitory potency of 5 nM .

Storage & Handling

• Storage: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

Desethyl Sacubitril, CD10, Cluster of differentiation 10, Neutral endopeptidase, Neprilysin, NEP, inhibit, LBQ657, LBQ-657, LBQ 657, Inhibitor, Sacubitrilat

Compound Identifiers

PubChem CID

10430040