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Cevimeline hydrochloride

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Catalog No. T20131Cas No. 107220-28-0
Alias Cevimeline HCl, AF102B hydrochloride, AF 102B hydrochloride

Cevimeline hydrochloride (AF102B hydrochloride) is a quinuclidine derivative of acetylcholine that functions as a selective, orally active muscarinic M1 and M3 receptor agonist. Cevimeline hydrochloride effectively stimulating exocrine secretion from salivary glands and thereby serving as a clinically relevant sialogogue for the treatment of xerostomia, while its demonstrated ability to cross the blood–brain barrier supports its utility in central and peripheral cholinergic signaling studies and translational neuropharmacological investigations.

Cevimeline hydrochloride

Cevimeline hydrochloride

😃Good
Catalog No. T20131Alias Cevimeline HCl, AF102B hydrochloride, AF 102B hydrochlorideCas No. 107220-28-0
Cevimeline hydrochloride (AF102B hydrochloride) is a quinuclidine derivative of acetylcholine that functions as a selective, orally active muscarinic M1 and M3 receptor agonist. Cevimeline hydrochloride effectively stimulating exocrine secretion from salivary glands and thereby serving as a clinically relevant sialogogue for the treatment of xerostomia, while its demonstrated ability to cross the blood–brain barrier supports its utility in central and peripheral cholinergic signaling studies and translational neuropharmacological investigations.
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2 mg$59-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Cevimeline hydrochloride (AF102B hydrochloride) is a quinuclidine derivative of acetylcholine that functions as a selective, orally active muscarinic M1 and M3 receptor agonist. Cevimeline hydrochloride effectively stimulating exocrine secretion from salivary glands and thereby serving as a clinically relevant sialogogue for the treatment of xerostomia, while its demonstrated ability to cross the blood–brain barrier supports its utility in central and peripheral cholinergic signaling studies and translational neuropharmacological investigations.
In vitro
In digested parotid gland cells, Cevimeline hydrochloride (0.1-100 μM) induced a concentration-dependent increase in intracellular Ca2+ triggering exocytosis [1].
In vivo
In male Wistar rats, intraperitoneal (i.p.) injection of Cevimeline hydrochloride (0.008-0.016 mg/kg) induces long-lasting salivation and increases parotid gland blood flow. Furthermore, Cevimeline hydrochloride inhibits water intake induced by Angiotensin II (AngII) [1][2][5].
SynonymsCevimeline HCl, AF102B hydrochloride, AF 102B hydrochloride
Chemical Properties
Molecular Weight235.77
FormulaC10H18ClOS
Cas No.107220-28-0
SmilesC[C@@H]1O[C@@]2([C@H]3CCN(C2)CC3)CS1.Cl
Relative Density.no data available
Storage & Solubility Information
Storagestore at low temperature | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: Soluble
H2O: 40 mg/mL (169.66 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM4.2414 mL21.2071 mL42.4142 mL212.0711 mL
5 mM0.8483 mL4.2414 mL8.4828 mL42.4142 mL
10 mM0.4241 mL2.1207 mL4.2414 mL21.2071 mL
20 mM0.2121 mL1.0604 mL2.1207 mL10.6036 mL
50 mM0.0848 mL0.4241 mL0.8483 mL4.2414 mL
100 mM0.0424 mL0.2121 mL0.4241 mL2.1207 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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%
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