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Tamsulosin hydrochloride
Cat. No.:
0225LY-1211
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
Tamsulosin hydrochloride is the hydrochloride salt form of tamsulosin, a sulfonamide derivative that exhibits alpha-1 adrenergic antagonist activity.
Synonym:
Flomax; Flomax hydrochloride; 106463-17-6; Omnic; Tamsulosin HCl; Pradif; Harnal; Urolosin; Secotex; Josir; Alna; Omic; Omix; Amsulosin hydrochloride; (R)-Tamsulosin Hydrochloride; (R)-5-(2-((2-(2-Ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide hydrochloride; Tamsulosin (hydrochloride); R-(-)-(-)-(R)-5-(2-((2-(o-Ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide monohydrochloride; 5-[(2R)-2-[[2-(2-Ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesulfonamide hydrochloride; 5-[(2R)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide;hydrochloride; R-(-)-5-(2-((2-(2-Ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide hydrochloride
CAS No.:
106463-17-6
Compound CID:
5362376
Formula:
C20H29ClN2O5S
Formula Weight:
444.97
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Tamsulosin hydrochloride can be used in prostate research to investigate the selective blockade of alpha-1A and alpha-1D adrenoceptors.
Library Information
Target:
α1A-Adrenergic receptor; α1B-Adrenergic receptor; α1D-Adrenergic receptor
Receptor:
GPCR
Pathways:
Neuronal signaling; GPCR/G protein signaling
Plate Number:
AOCL-16
Plate Location:
e8
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
50 mg/mL; 112.37 mM
Water Max Solubility:
4.5 mg/mL; 10.11 mM
