Donepezil HCl

Catalog No.S2462 Batch:S246202

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Technical Data

Formula

C24H29NO3.HCl

Molecular Weight 416 CAS No. 120011-70-3
Solubility (25°C)* In vitro Water 5 mg/mL (12.01 mM)
DMSO Insoluble
Ethanol Insoluble
In vivo (Add solvents to the product individually and in order)
Clear solution
30%propylene glycol 5%Tween80 65%D5W
30.0mg/ml Taking the 1 mL working solution as an example, add 300 μL of 100 mg/ml clarified propylene glycol stock solution to 50 μL of Tween 80, mix evenly to clarify it; then continue to add 650 μL of D5W to adjust the volume to 1 mL. The mixed solution should be used immediately for optimal results. 
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description Donepezil is a specific and potent AChE inhibitor for bAChE and hAChE with IC50 of 8.12 nM and 11.6 nM , respectively.
Targets
bAChE [1] hAChE [1]
8.12 nM 11.6 nM
In vitro Donepezil inhibits the carbachol-stimulated increase in intracellular Ca2+ concentration in human SHSY5Y neuroblastoma cells in a concentration dependent manner, indicating that Donepezil have muscarinic antagonist activity. [2] A recent study shows that Donepezil can protect human umbilical vein endothelial cells (HUVECs) against H2O2-induced cell injury. This may be useful as a potential therapy for oxidative stress in cardiovascular and cerebrovascular diseases. [3]
In vivo Intraperitoneal administration of Donepezil in rats produces a dose dependent increase in salivation and tremor, which are overt cholinergic behavioural signs, with an ED50 of 6 μmol/kg. Donepezil is found to be somewhat less potent with a ED50 of 50 μmol/kg following oral administration. [2]. When administered separately in vivo, 5-HT(4) receptor inducer, RS67333 (0.3 and 1 mg/kg) and Donepezil (1 mg/kg) improves recognition performances compared to saline treated mice, while co-administration of subactive doses of RS67333 (0.1mg/kg) and Donepezil (0.3 mg/kg) improves memory. However, this improvement is prevented if a 5-HT(4)R antagonist (GR125487, 10 mg/kg) is also administered. [4]

Protocol (from reference)

Animal Study:[2]
  • Animal Models

    Male Lister Hooded rats

  • Dosages

    18 μM/kg

  • Administration

    Administered via i.p. or p.o.

Customer Product Validation

Data from [Data independently produced by J Am Heart Assoc, 2014, 3(3), e000804]

Data from [Data independently produced by , , Anal Bioanal Chem, 2017, 409(28):6635-6642]

Selleck's Donepezil HCl has been cited by 10 publications

Inhibition of Th17 cells by donepezil ameliorates experimental lung fibrosis and pulmonary hypertension [ Theranostics, 2023, 13(6):1826-1842] PubMed: 37064881
Antidementia medication acetylcholinesterase inhibitors have therapeutic benefits on osteoporotic bone by attenuating osteoclastogenesis and bone resorption [ J Cell Physiol, 2023, 10.1002/jcp.31057] PubMed: 37334837
Protective effect of Huanglianjiedu Decoction on microcystin-LR induced nerve injury [ Comp Biochem Physiol C Toxicol Pharmacol, 2023, 272:109698] PubMed: 37442312
Intratarget Microdosing for Deep Phenotyping of Multiple Drug Effects in the Live Brain [ Front Bioeng Biotechnol, 2022, 10:855755] PubMed: 35372313
A study of protein-drug interaction based on solvent-induced protein aggregation by fluorescence correlation spectroscopy [ Analyst, 2022, 10.1039/d2an00031h] PubMed: 35253833
Donepezil Ameliorates Pulmonary Arterial Hypertension by Inhibiting M2-Macrophage Activation [ Front Cardiovasc Med, 2021, 8:639541] PubMed: 33791350
Reduced TRPC6 mRNA levels in the blood cells of patients with Alzheimer's disease and mild cognitive impairment [Lu R Mol Psychiatry, 2018, 23(3):767-776] PubMed: 28696436
Aging-related Repositioned Drugs, Donepezil and Sildenafil Citrate, Increase Apoptosis of Anti-mitotic Drug-resistant KBV20C Cells Through Different Molecular Mechanisms [Kim JY Anticancer Res, 2018, 38(9):5149-5157] PubMed: 30194162
A microfluidics-based mobility shift assay to identify new inhibitors of β-secretase for Alzheimer's disease [Liu R Anal Bioanal Chem, 2017, 409(28):6635-6642] PubMed: 28889204
Arterial baroreflex dysfunction impairs ischemia-induced angiogenesis [Hao C, et al J Am Heart Assoc, 2014, 3(3):e000804] PubMed: 24820655

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.