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Flavoxate hydrochloride

Catalog No. T0703   CAS 3717-88-2
Synonyms: Flavoxate HCl, NSC-114649, DW61, Rec-7-0040

Flavoxate hydrochloride (DW61) , a muscarinic AChR antagonist, is used in the therapy of various urinary syndromes and as an antispasmodic.

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Flavoxate hydrochloride Chemical Structure
Flavoxate hydrochloride, CAS 3717-88-2
Pack Size Availability Price/USD Quantity
25 mg In stock $ 30.00
50 mg In stock $ 43.00
100 mg In stock $ 58.00
200 mg In stock $ 63.00
1 g In stock $ 89.00
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Purity: 99.64%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Flavoxate hydrochloride (DW61) , a muscarinic AChR antagonist, is used in the therapy of various urinary syndromes and as an antispasmodic.
Targets&IC50 mAChR:12.2 μM
In vitro Without altering basal bladder pressure in rats, Flavoxate (3 mg/kg) can halt efferent nerve activity and associated bladder contractions for approximately 10 minutes. At the same dosage, administered intravenously, Flavoxate abolishes rhythmic bladder contractions, with maximum intervals of voiding contractions reaching 7.20 minutes. In rats, at a higher concentration (10 mg/kg), Flavoxate suppresses both the initial rapid-rise contraction phase (Phase 1) and the sustained contraction phase (Phase 2) to an equivalent degree. Furthermore, at this concentration, Flavoxate eliminates bladder contractions without altering contraction amplitude. Intracerebroventricular (ICV) injections of Flavoxate ranging from 50 to 200 mg or intrathecal (IT) injections of 100 to 200 mg dose-dependently abolish rhythmic bladder contractions within 5 to 15 minutes post-administration.
In vivo Flavoxate inhibits cAMP formation in a concentration-dependent manner (0.01~10 μM) from membranes extracted from the rat cerebral cortex and striatum, an effect completely negated by pertussis toxin pretreatment. At concentrations greater than 10 μM, Flavoxate suppresses detrusor muscle contraction induced by acetylcholine, with a pD value of 4.55, and also inhibits contractions induced by Ca2+, with a pIC50 value of 4.92. Flavoxate concentration-dependently reduces K+-induced contractions of human bladder. It can displace [3H]nitrendipine at Ca2+ channel binding sites, with an IC50 of 254 μM. Flavoxate also concentration- and voltage-dependently inhibits the peak amplitude of inward Ba2+ currents sensitive to the voltage-dependent nifedipine in human detrusor smooth muscle cells (Ki: 10 μM), and inhibits the same Ba2+ currents at both 30°C (Ki = 5.1 mM) and 37°C (Ki = 4.6 mM).
Synonyms Flavoxate HCl, NSC-114649, DW61, Rec-7-0040
Molecular Weight 427.92
Formula C24H26ClNO4
CAS No. 3717-88-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 2.5 mM

TargetMolReferences and Literature

1. Dansette PM, et al. Exp Toxicol Pathol, 2000, 52(2), 145-148. 2. Kimura Y, et al. Int J Urol, 1996, 3(3), 218-227. 3. Oka M, et al. Brain Res, 1996, 727(1-2), 91-98. 4. Tomoda T, et al. Br J Pharmacol, 2005, 146(1), 25-32. 5. Tomoda T, et al. Naunyn Schmiedebergs Arch Pharmacol, 2007, 376(3), 195-203.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Neurodegenerative Disease Compound Library Inhibitor Library Drug Repurposing Compound Library Membrane Protein-targeted Compound Library FDA-Approved Drug Library Anti-Aging Compound Library Drug-induced Liver Injury (DILI) Compound Library FDA-Approved & Pharmacopeia Drug Library Neurotransmitter Receptor Compound Library Anti-Alzheimer's Disease Compound Library

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Keywords

Flavoxate hydrochloride 3717-88-2 Neuroscience AChR lower urinary tract infections Phosphodiesterase Calcium Channel mAChR anesthetic overactive bladder Flavoxate HCl Ca2+ channels DW-61 Ca channels Inhibitor NSC-114649 antispasmodic DW61 inhibit NSC114649 muscarinic NSC 114649 DW 61 Muscarinic acetylcholine receptor Flavoxate Hydrochloride Rec-7-0040 Phosphodiesterase (PDE) Flavoxate inhibitor

 

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