LY2795050

CAS No. 1346133-08-1

LY2795050( —— )

Catalog No. M23506 CAS No. 1346133-08-1

LY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 105 In Stock
5MG 177 In Stock
10MG 285 In Stock
25MG 470 In Stock
50MG 672 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LY2795050
  • Note
    Research use only, not for human use.
  • Brief Description
    LY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).
  • Description
    LY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).
  • In Vitro
    LY2795050 displays high affinity with a Ki value of 0.72 nM for the KOR and has antagonist activity with a Kb value of 0.63 nM.
  • In Vivo
    LY2795050 (i.p., 0.032-0.1mg/kg, 30 min) prevents dose-dependent grooming deficits produced by U50,488 in male and female mice.LY2795050 (i.p., 0.032-0.1mg/kg, 0-150 min) has sexual dimorphism in some behavioral effects. Animal Model:C57BL/6J mice(gonadally intact, adult, male and female)Dosage:0.032-0.1 mg/kg Administration:i.p., 0.032-0.1mg/kg, 30 minResult:Could dose-dependently prevent the self-grooming deficits caused by U50,488 with a 30-min pre-treatment.Not effected in blocking the effects of U50,488 with smaller dose (0.032mg/kg) in either males or females.Decreased immobility in the FST in males at a dose of 0.1mg/kg, but not in females, up to a dose of 0.32mg/kg.Prevented and also reversed (at 0.32mg/kg) the locomotor-depressant effects of U50,488 (10mg/kg), in males and females.
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    κ-opioid receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1346133-08-1
  • Formula Weight
    407.89
  • Molecular Formula
    C23H21ClN3O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:50 mg/mL (122.58 mM; Need ultrasonic)
  • SMILES
    O=C(N)C1=CC=C(OC2=CC=C(CN3[C@H](C4=CC=CN=C4)CCC3)C=C2)C(Cl)=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Mitch, Charles H.; Quimby, Steven J.; Diaz, Nuria; et al. Discovery of Aminobenzyloxyarylamides as κ Opioid Receptor Selective Antagonists: Application to Preclinical Development of a κ Opioid Receptor Antagonist Receptor Occupancy Tracer. Journal of Medicinal Chemistry (2011), 54(23), 8000-8012.
molnova catalog
related products
  • (-)-U-50488 hydrochl...

    The more active enantiomer of (±)-U-50488, a potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects.

  • 6-GNTI dihydrochlori...

    6'-GNTI dihydrochloride is a κ-opioid receptor (KOR) agonist that favors activation of G-protein-mediated signaling over recruitment of β-aspirin 2. 6'-GNTI dihydrochloride only activates the Akt pathway in striatal neurons.

  • [Nphe1]Nociceptin(1-...

    Selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.