SKU:K1384 | M. Wt:495.53 | ||
Formula:C25H32F3N3O4 | Solubility:No | ||
Purity:>99% | Storage:2 years at -20 degrees centigrade | ||
CAS No.:160970-54-7 | Synonyms:KAD 3213, KMD 3213 | ||
Chemical NameN/A |
供货周期: | 一周 |
品牌: | |
规格: | 2mg |
货号: | K1384 |
CAS号: | 160970-54-7 |
SKU:K1384 | M. Wt:495.53 | ||
Formula:C25H32F3N3O4 | Solubility:No | ||
Purity:>99% | Storage:2 years at -20 degrees centigrade | ||
CAS No.:160970-54-7 | Synonyms:KAD 3213, KMD 3213 | ||
Chemical NameN/A |
Description | Silodosin (Rapaflo) | |||||
---|---|---|---|---|---|---|
Targets | alpha(1)-adrenoceptor | |||||
IC50 | N/A | |||||
In vitro | KMD 3213(silodosin, KAD 3213) is an orally active alpha(1)-adrenoceptor antagonist.[1] Silodosin shows higher selectivity for the alpha(1A)-AR subtype than tamsulosin hydrochloride, naftopidil or prazosin hydrochloride.Silodosin strongly antagonizes noradrenaline-induced contractions in rabbit lower urinary tract tissues.[2] silodosin inhibits the phenylephrine-induced increase in intraurethral pressure for a longer time than tamsulosin hydrochloride.[3] | |||||
In vivo | Silodosin is a dual substrate for CYP3A4 and p-glycoprotein. After a single oral dose of (14)C-silodosin in rat, dog and human, the urinary excretion of radioactivity was 15-34%, with that of unchanged silodosin being less than 4%.[4]Intravenously (i.v.) administered silodosin dose-dependently inhibited the HNS-induced increase in IUP with much less hypotensive effect than either tamsulosin or naftopidil, the uroselectivity (ED(15)/ID(50)) of silodosin (237) being significantly higher than those of tamsulosin (1.21) and naftopidil (2.65).[5] | |||||
Clinical Trials | N/A | |||||
Features | N/A |
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