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ChemicalBook Product Catalog API Urinary System Drugs Other Urinary System Drugs Tamsulosin hydrochloride

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Tamsulosin hydrochloride NEW

$30.00 10mg

$48.00 25mg

$68.00 50mg

Min. Order
Purity99.95%
Cas No106463-17-6
Supply Ability10g
Update time2024-11-20

TargetMol Chemicals Inc.

TargetMol Chemicals Inc.

5YR

United States

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Chemical Properties

Product Name	Tamsulosin hydrochloride
CAS No	106463-17-6
EC-No
Min. Order
Purity	99.95%
Supply Ability	10g
Release date	2024/11/20

Product Introduction

Bioactivity

Name	Tamsulosin hydrochloride
Description	Tamsulosin hydrochloride (Flomax hydrochloride) is the hydrochloride salt of tamsulosin, a sulfonamide derivative with α1 adrenergic antagonist activity.
In vivo	Tamsulosin exhibits high plasma-protein binding, largely to α1-acid glycoprotein. It is metabolized, mainly by cytochrome P450 (CYP) 3A4 and CYP2D6 to compounds with low abundance, and 8.7–15% of an oral dose is excreted renally as the parent compound. The pharmacokinetics of tamsulosin are not affected to a major extent by age, and pharmacokinetic alterations in renally impaired patients relate largely to an increased concentration of α1-acid glycoprotein. Pharmacokinetic alterations with hepatic impairment are also only moderate, thus neither renal nor mild to moderate hepatic impairment necessitates dose adjustment. Early studies of tamsulosin IR in experimental animals, such as rats and dogs, showed rapid absorption of tamsulosin after oral administration (within 30–90 minutes) but absolute bioavailability of only 7–23% in rats and 30–42% in dogs. The absolute bioavailability of tamsulosin MR in fasted humans is approximately 100%. The tmax is typically about 5 hours (reported range of mean values 2.9-5.6 hours) in the fasted state and about 6 hours in the fed state (range 5.2-7.0 hours). Animal studies involving intravenous injection of radiolabelled tamsulosin and measurement of radiolabel in various tissues after 10 minutes have shown the presence of the drug in various tissues, ranked in the following order: kidney>lung≈heart>submaxillary gland>liver ≈spleen≈aorta≈vas deferens> prostate>>cerebral cortex, the latter being close to detection limits. Tamsulosin may not pass the blood-brain barrier.
Storage	Powder: -20°C for 3 years \| In solvent: -80°C for 1 year \| Shipping with blue ice.
Solubility Information	DMSO : 50 mg/mL (112.37 mM) H2O : 4.5 mg/mL (10 mM)
Keywords	Adrenergic Receptor \| LY 253351 \| LY-253351 \| Tamsulosin hydrochloride \| Inhibitor \| LY253351 \| Beta Receptor \| inhibit \| Tamsulosin \| Flomax Hydrochloride \| Tamsulosin Hydrochloride
Inhibitors Related	Olanzapine \| Mirtazapine \| Octopamine hydrochloride \| Gemfibrozil \| Dexmedetomidine hydrochloride \| Phenylephrine hydrochloride \| Isoprenaline hydrochloride \| Amitriptyline hydrochloride \| Trazodone hydrochloride \| Mianserin hydrochloride
Related Compound Libraries	Bioactive Compound Library \| Anti-Neurodegenerative Disease Compound Library \| Membrane Protein-targeted Compound Library \| Anti-Cancer Clinical Compound Library \| Drug Repurposing Compound Library \| Inhibitor Library \| Anti-Cancer Approved Drug Library \| Bioactive Compounds Library Max \| GPCR Compound Library \| Anti-Cancer Drug Library

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