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Bethanechol (chloride)

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    Bethanechol (chloride)
  • Bethanechol (chloride)
Cat No: 23830
Biochemicals - Receptor Pharmacology
Cayman

Bethanechol is an agonist of muscarinic acetylcholine receptors with IC50 values of 1,837, 25, 631, 317, and 393 µM for M1-5, respectively, in a radioligand binding assay using CHO cells expressing the human receptors.{40682} It inhibits M2-mediated ...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2-[(aminocarbonyl)oxy]-N,N,N-trimethyl-1-propanaminium, monochloride
Correlated keywords:
  • 674-38-4 21293-39-0 Urecholine Besacholine NSC30783 Carbamylmethylcholine Mechotane Mechothane Mecothane Mictone Myocholine Myotonachol Trimethyl(2-carbamoyloxypropyl)ammonium Uro-Carb Myotonine ?-Methyl carbachol M-1 2 5 M5 cAMP
Product Overview:
Bethanechol is an agonist of muscarinic acetylcholine receptors with IC50 values of 1,837, 25, 631, 317, and 393 µM for M1-5, respectively, in a radioligand binding assay using CHO cells expressing the human receptors.{40682} It inhibits M2-mediated increases in cyclic AMP induced by isoproterenol (Item No. 15592) in isolated guinea pig small intestine (IC50 = 127 µM).{18340} Bethanechol increases basal tone of isolated porcine intravesical ureter (EC50 = 4.27 µM).{27105} It also induces fluid secretion in the ileum, duodenum, and jejunum of anesthetized rats when administered at a dose of 60 µg/kg.{40787} Formulations containing bethanechol have been used to increase urination and improve smooth muscle tone in the gastrointestinal tract.
Size 1 g
Shipping dry ice
CAS Number 590-63-6
Molecular Formula C7H17N2O2 • Cl
SMILES CC(OC(N)=O)C[N+](C)(C)C.[Cl-]
Molecular Weight 196,7
Formulation A crystalline solid
Purity ≥95%
Custom Code 2921.29
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO Guide 34:2009

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