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Bethanechol chloride

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Catalog No. T3126Cas No. 590-63-6
Alias Urecholine, Myocholine, Carbamyl-β-methylcholine chloride, (±)-Bethanechol

Bethanechol chloride (Carbamyl-β-methylcholine chloride) is a slowly hydrolyzing muscarinic agonist with no nicotinic effects. It is used to increase smooth muscle tone in the GI tract following abdominal surgery or to treat urinary retention without obstruction. Possible side effects include hypotension, heart rate changes, and bronchial spasm.

Bethanechol chloride

Bethanechol chloride

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Purity: 99.73%
Catalog No. T3126Alias Urecholine, Myocholine, Carbamyl-β-methylcholine chloride, (±)-BethanecholCas No. 590-63-6
Bethanechol chloride (Carbamyl-β-methylcholine chloride) is a slowly hydrolyzing muscarinic agonist with no nicotinic effects. It is used to increase smooth muscle tone in the GI tract following abdominal surgery or to treat urinary retention without obstruction. Possible side effects include hypotension, heart rate changes, and bronchial spasm.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$30-In Stock
1 g$37-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.73%
Color:White
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Product Introduction

Bethanechol chloride AI Summary
Bethanechol chloride exhibits agonist activity at muscarinic receptors M2, M3, and M4 in guinea pig tissues, with specific potency (pD2 values) of 5.59, 6.26, and 4.68 respectively. It also shows inhibition of electrically-stimulated muscle contraction with pD2 values of 5.01, 6.16, and 5.88 for M2, M3, and M4 receptors, respectively. The compound has intrinsic activity of 1.0 at these muscarinic receptors relative to McN-A-343. Additionally, Bethanechol chloride inhibits sodium fluorescein uptake in OATP1B1 and OATP1B3-transfected CHO cells with inhibition percentages of 111.12% and 100.03% respectively at a concentration of 10 µM, indicating strong bioactivity in blocking the uptake of sodium fluorescein. It also exhibits multiple bioactivities such as inhibiting Tau fibril formation, G9a histone lysine methyltransferase, and ERG Ets/DNA interaction. Furthermore, it induces DNA re-replication in both normal breast and colon adenocarcinoma cells and shows differential inhibition of Plasmodium falciparum proliferation, leading to delayed death of the malarial parasite plastid. The compound exhibits minimal antiviral activity in Vero E6 cells against SARS-CoV-2 after 72 hours (inhibition index 0.1188) and modest activity in inhibiting SARS-CoV-2 3CL-Pro protease (3.916% at 20 µM). Additionally, it demonstrates 35.01% inhibition of SARS-CoV-2-induced cytotoxicity in Caco-2 cells at a concentration of 10 µM after 48 hours. It also has low antifungal activity against Candida albicans and Cryptococcus neoformans, while exhibiting variable antibacterial activity against several bacterial strains, including Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Staphylococcus aureus MRSA..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Bethanechol chloride (Carbamyl-β-methylcholine chloride) is a slowly hydrolyzing muscarinic agonist with no nicotinic effects. It is used to increase smooth muscle tone in the GI tract following abdominal surgery or to treat urinary retention without obstruction. Possible side effects include hypotension, heart rate changes, and bronchial spasm.
SynonymsUrecholine, Myocholine, Carbamyl-β-methylcholine chloride, (±)-Bethanechol
Chemical Properties
Molecular Weight196.68
FormulaC7H17N2O2·Cl
Cas No.590-63-6
Smiles[Cl-].O(C(C[N+](C)(C)C)C)C(=O)N
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from direct sunlight | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 36 mg/mL (183.04 mM), Sonication is recommended.
DMSO: 37 mg/mL (188.12 mM), Sonication is recommended.
Ethanol: 37 mg/mL (188.12 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO/Ethanol
1mg5mg10mg50mg
1 mM5.0844 mL25.4220 mL50.8440 mL254.2201 mL
5 mM1.0169 mL5.0844 mL10.1688 mL50.8440 mL
10 mM0.5084 mL2.5422 mL5.0844 mL25.4220 mL
20 mM0.2542 mL1.2711 mL2.5422 mL12.7110 mL
50 mM0.1017 mL0.5084 mL1.0169 mL5.0844 mL
100 mM0.0508 mL0.2542 mL0.5084 mL2.5422 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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