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Postion:Product Catalog >Biochemical Engineering>Inhibitors>Neuronal Signaling>AChR antagonist>Fesoterodine fumarate
Fesoterodine fumarate
  • Fesoterodine fumarate

Fesoterodine fumarate NEW

Price $47 $77 $113
Package 5mg 10mg 25mg
Min. Order:
Supply Ability: 10g
Update Time: 2024-11-19

Product Details

Product Name: Fesoterodine fumarate CAS No.: 286930-03-8
Purity: 98.55% Supply Ability: 10g
Release date: 2024/11/19

Product Introduction

Bioactivity

NameFesoterodine fumarate
DescriptionFesoterodine fumarate (Toviaz) is the fumarate salt form of fesoterodine, a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. Fesoterodine is rapidly hydrolyzed in vivo into its active metabolite 5-hydroxymethyl tolterodine, which binds and inhibits muscarinic receptors on the bladder detrusor muscle, thereby preventing bladder contractions or spasms caused by acetylcholine.
In vitroFesoterodine is rapidly and extensively converted to 5-HMT, such that the pharmacologic activity appears to be primarily attributable to 5-HMT. [1] Fesoterodine is a competitive antagonist of cholinergic agonist-stimulated responses in human M1-M5 cell lines and has a similar potency and selectivity profile to the radioligand-binding studies. Fesoterodine causes a rightward shift of the concentration-response curve for carbachol with no depression of the maximum in rat bladder strips, and concentration-dependently reduces contractions induced by electrical field stimulation (EFS). [2] Fesoterodine is hydrolyzed by nonspecific esterases to 5-hydroxmethyl tolterodine (5-HMT), which is the active metabolite and is responsible for all its antimuscarinic activity. [3]
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 93 mg/mL (176.3 mM)
H2O : 92 mg/mL (174.4 mM)
Ethanol : 93 mg/mL (176.3 mM)
Keywords5-HMT | antimuscarinic | SPM-907 | muscarinic | mAChR | overactive | Fesoterodine Fumarate | inhibit | OAB | Fesoterodine | receptor | SPM7605 | Muscarinic acetylcholine receptor | bladder | Desfesoterodine | SPM907 | Inhibitor | Fesoterodine fumarate | orally
Inhibitors RelatedAdiphenine hydrochloride | Ribavirin | Choline chloride | Propoxur
Related Compound LibrariesBioactive Compound Library | Anti-Neurodegenerative Disease Compound Library | Membrane Protein-targeted Compound Library | EMA Approved Drug Library | Drug Repurposing Compound Library | Inhibitor Library | FDA-Approved Drug Library | Bioactive Compounds Library Max

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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