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Results for "

Silodosin

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

3

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-10122
    Silodosin
    2 Publications Verification

    KAD 3213; KMD 3213

    		 Adrenergic Receptor Bacterial Endocrinology Cancer
    Silodosin (KAD 3213; KMD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH .
    <em>Silodosin</em>
  • HY-144165S
    Silodosin metabolite-d4

    		Isotope-Labeled Compounds Others
    Silodosin metabolite-d4 is the deuterium labeled Silodosin metabolite[1].
    <em>Silodosin</em> metabolite-d4
  • HY-10122R
    Silodosin (Standard)

    		Adrenergic Receptor Bacterial Endocrinology Cancer
    Silodosin (Standard) is the analytical standard of Silodosin. This product is intended for research and analytical applications. Silodosin (KAD 3213; KMD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH .
    <em>Silodosin</em> (Standard)
  • HY-144166S
    Silodosin glucuronide-d4 lithium

    		Isotope-Labeled Compounds Others
    Silodosin glucuronide-d4 (lithium) is the deuterium labeled Silodosin glucuronide lithium[1].
    <em>Silodosin</em> glucuronide-d4 lithium
  • HY-10122S
    Silodosin-d4

    		Isotope-Labeled Compounds Adrenergic Receptor Endocrinology Cancer
    Silodosin-d4 is the deuterium labeled Silodosin. Silodosin (KAD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH[1][3].
    <em>Silodosin</em>-d4

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