Spiradoline mesylate

CAS No. 87173-97-5

Spiradoline mesylate( U 62066 )

Catalog No. M16337 CAS No. 87173-97-5

Spiradoline (U 62066) is a potent, highly selective κ-opioid agonist that has analgesic diuretic and antitussive effects.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Spiradoline mesylate
  • Note
    Research use only, not for human use.
  • Brief Description
    Spiradoline (U 62066) is a potent, highly selective κ-opioid agonist that has analgesic diuretic and antitussive effects.
  • Description
    Spiradoline (U 62066) is a potent, highly selective κ-opioid agonist that has analgesic diuretic and antitussive effects.Pain Phase 2 Discontinued.
  • In Vitro
    Using the patch-clamp method in isolated rat cardiac myocytes, indicated that Spiradoline mesylate (15 to 500 μM) produces its antiarrythmic effect via blockade of sodium channels (and at the higher doses also of potassium currents) in myocardial tissue. Thus, Spiradoline mesylate reduces the peak sodium current, increased the decay rate of the transient outward potassium current, and reduced the sustained plateau potassium amplitude.
  • In Vivo
    Spiradoline mesylate (U-62066; 0.1-0.4 mg/kg; subcutaneous injection; once; Sprague-Dawley rats) treatment dose-dependently reduces social behaviors in non-stressed adults, producing social avoidance at the highest dose tested, while younger animals displays reduced sensitivity to this socially suppressing effect of Spiradoline mesylate. In stressed animals, the socially suppressing effects of the Spiradoline mesylate are blunted at all ages, with juveniles and adolescents exhibiting increased social preference in response to certain doses of U-62066. Animal Model:Juvenile, adolescent and adult Sprague-Dawley male and female rats exposured to repeated restraint Dosage:0.1 mg/kg, 0.2 mg/kg, 0.3 mg/kg, and 0.4?mg/kg Administration:Subcutaneous injection; once Result:Dose-dependently reduced social behaviors in non-stressed adults, producing social avoidance at the highest dose tested.
  • Synonyms
    U 62066
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    Opioid Receptor
  • Research Area
    Neurological Disease
  • Indication
    Pain

Chemical Information

  • CAS Number
    87173-97-5
  • Formula Weight
    521.494
  • Molecular Formula
    C23H34Cl2N2O5S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ClC1=C(Cl)C=CC(CC(N(C)[C@H]2CC[C@]3(OCCC3)C[C@@H]2N4CCCC4)=O)=C1.CS(O)(=O)=O
  • Chemical Name
    2-(3,4-dichlorophenyl)-N-methyl-N-[(5R,7S,8S)-7-pyrrolidin-1-yl-1-oxaspiro[4.5]decan-8-yl]acetamide mesylate

Shipping & Storage Information

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

Reference

1. Peters GR, et al. J Pharmacol Exp Ther. 1987 Jan;240(1):128-31. 2. Kamei J, et al. Eur J Pharmacol. 1990 Oct 9;187(2):281-6. 3. Kunihara M, et al. Life Sci. 1989;45(13):1191-8.
molnova catalog
related products
  • L-Menthol

    Menthol is a covalent organic compound made synthetically or obtained from peppermint or other mint oils.

  • Loperamide hydrochlo...

    Loperamide HCl is an opioid-receptor agonist used as long-acting synthetic antidiarrheals.

  • Adrenorphin(3TFA)

    Adrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).