l General Information |
Product Name | Flavoxate HCl |
General description | Flavoxate HCl is a muscarinic AChR antagonist with IC50 of 12.2 μM. |
Synonym | NSC-114649; 2-piperidin-1-ylethyl 3-methyl-4-oxo-2-phenylchromene-8-carboxylate;hydrochloride |
Purity | ≥99.0%(HPLC) | CAS Number | 3717-88-2 |
Formula | C24H26ClNO4 | Molecular Weight | 427.925 |
Suitability | BioReagent, suitable for cell culture, etc. |
l Physical and Chemical Information |
Appearance | White to off-white Solid |
Solubility(25°C) | DMSO | Very slightly soluble |
Ethanol | Insoluble |
Water | ~5mg/ml |
l Biological Information |
Biochem/Physiol
Actions | Flavoxate Hydrochloride is the hydrochloride salt form of flavoxate, a parasympatholytic agent with antispasmodic activity. Flavoxate hydrochloride competitively binds to muscarinic receptors, thereby preventing the actions of acetylcholine. This relaxes vascular smooth muscle, mainly of the urinary tract, and prevents smooth muscle contractions. |
Application | 1.Parasympatholytics 2.Urological Agents |
l Storage |
Storage temp. | -20°C |
l Precautions and Disclaimer |
This product is for R&D use only, not for drug, household, or other uses. |
l References |
1. http://www.drugbank.ca 2. https://ncit.nci.nih.gov 3. https://www.ncbi.nlm.nih.gov |
