
Ensitrelvir Fumaric Acid
A orally active non-covalent, non-peptidic, SARS-CoV-2 3CL protease inhibitor (IC50=13 nM).
Overview
Ensitrelvir Fumaric Acid is an effective oral antiviral drug and a 3CL protease inhibitor, which has the effect of inhibiting the replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Ensitrelvir Fumaric Acid can be used in research on the treatment of SARS-CoV-2 infection, viral replication mechanism and related antiviral drug development.
Synonyms: S-217622; Xocova; Ensitrelvir; RMA-43; S-217622 fumarate; S-217622-002-C4H4O4; Ensitrelvir fumarate; Ensitrelvir fumarate(S-217622)
Product Categories: Heterocyclic Compounds; Aromatics; Pharmaceuticals; Intermediates & Fine Chemicals; API (Active Pharmaceutical Ingredient)
Mol File: 2757470-18-9.mol
Physicochemical Properties
Storage temp: -20℃
Solubility: DMSO:0.0(Max Conc. mg/mL);0.0(Max Conc. mM)
Form: Solid
Color: White to Off-white
MSDS Information
Experimental Data
1. Cell Experiment
DMSO : 100 mg/mL (154.33 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Preparing Stock Solutions:

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
2. Animal Experiment
Select the appropriate dissolution method based on your experimental animal and administration route.
For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Protocol 1
Add each solvent one by one: 10% DMSO, 40% PEG300, 5% Tween-80, 45% Saline
Solubility: 2.5 mg/mL (3.86 mM); Suspended solution; Need ultrasonic
This protocol yields a suspended solution of 2.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Protocol 2
Add each solvent one by one: 10% DMSO, 90% (20% SBE-β-CD in Saline)
Solubility: 2.5 mg/mL (3.86 mM); Suspended solution; Need ultrasonic
This protocol yields a suspended solution of 2.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Protocol 3
Add each solvent one by one: 10% DMSO, 90% Corn Oil
Solubility: ≥ 2.5 mg/mL (3.86 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.
Pharmacodynamics
Mechanism Of Action
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