Silodosin

CAS No. 160970-54-7

Silodosin ( KAD 3213;KMD 3213 )

Catalog No. M12319 CAS No. 160970-54-7

A highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 29 In Stock
10MG 47 In Stock
25MG 68 In Stock
50MG 82 In Stock
100MG 97 In Stock
200MG 122 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Silodosin
  • Note
    Research use only, not for human use.
  • Brief Description
    A highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively.
  • Description
    A highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively; inhibits norepinephrine-induced increases intracellular Ca2+ concentrations in CHO cells with IC50 of 0.32 nM; inhibits intraurethral pressure (IUP) response in vivo.Other Indication Approved
  • Synonyms
    KAD 3213;KMD 3213
  • Pathway
    Angiogenesis
  • Target
    Adrenergic Receptor
  • Recptor
    β-adrenergicreceptor
  • Research Area
    Other Indications
  • Indication
    Other Disease

Chemical Information

  • CAS Number
    160970-54-7
  • Formula Weight
    495.53
  • Molecular Formula
    C25H32F3N3O4
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C(C1=CC(C[C@H](NCCOC2=CC=CC=C2OCC(F)(F)F)C)=CC3=C1N(CCCO)CC3)N
  • Chemical Name
    1H-Indole-7-carboxamide, 2,3-dihydro-1-(3-hydroxypropyl)-5-[(2R)-2-[[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Shibata K, et al. Mol Pharmacol. 1995 Aug;48(2):250-8.
2. Yamagishi R, et al. Eur J Pharmacol. 1996 Nov 7;315(1):73-9.
3. Yamada S, et al. Life Sci. 1998;62(17-18):1585-9.
4. Akiyama K, et al. J Pharmacol Exp Ther. 1999 Oct;291(1):81-91.
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