Tamsulosin is a potent and selective α1a adrenergic receptor antagonist.
Tamsulosin exhibits high plasma-protein binding, largely to α1-acid glycoprotein. It is metabolized, mainly by cytochrome P450 (CYP) 3A4 and CYP2D6 to co
For research use only. We do not sell to patients.
Name | Tamsulosin hydrochloride |
---|---|
Iupac Chemical Name | Tamsulosin hydrochloride |
Synonyms | Tamsulosina hydrochloride, Tamsulosinum hydrochloride |
Molecular Formula | C20H28N2O5S·HCl |
Molecular Weight | 444.97 |
Smile | CCOc1ccccc1OCCN[C@H](C)Cc2ccc(c(c2)S(=O)(=O)N)OC.Cl |
InChiKey | ZZIZZTHXZRDOFM-XFULWGLBSA-N |
InChi | InChI=1S/C20H28N2O5S.ClH/c1-4-26-17-7-5-6-8-18(17)27-12-11-22-15(2)13-16-9-10-19(25-3)20(14-16)28(21,23)24;/h5-10,14-15,22H,4,11-13H2,1-3H3,(H2,21,23,24);1H/t15-;/m1./s1 |
CAS Number | 106463-17-6 |
MDL | MFCD00922997 |
Related CAS |
Packaging | Price | Availability | Purity | Shipping Time |
---|---|---|---|---|
Bulk | Enquiry | Enquiry | Enquiry |
Formulation | crystalline solid |
---|---|
Purity | 98% |
Storage | 3 years -20℃powder |
Solubility | Soluble in DMSO |
Handling | |
Shipping Condition | Shipped under ambient temperature as non-hazardous chemical. |
HS Code |
Targets | |
---|---|
Mechanism | |
Cell study | |
Animal study | |
Clinical study |