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 |
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| 5MG | 177 | In Stock |
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| 10MG | 285 | In Stock |
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| 25MG | 470 | In Stock |
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| 50MG | 672 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameLY2795050
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NoteResearch use only, not for human use.
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Brief DescriptionLY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).
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DescriptionLY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).
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In VitroLY2795050 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.
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In VivoLY2795050 (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.
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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Recptorκ-opioid receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number1346133-08-1
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Formula Weight407.89
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Molecular FormulaC23H21ClN3O2
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Purity>98% (HPLC)
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SolubilityDMSO:50 mg/mL (122.58 mM; Need ultrasonic)
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SMILESO=C(N)C1=CC=C(OC2=CC=C(CN3[C@H](C4=CC=CN=C4)CCC3)C=C2)C(Cl)=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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.
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