ChemicalBook--->CAS DataBase List--->1346133-08-1

1346133-08-1

1346133-08-1 Structure

1346133-08-1 Structure
IdentificationBack Directory
[Name]

LY-2795050
[CAS]

1346133-08-1
[Synonyms]

LY2795050
LY-2795050
LY 2795050
LY 2795050; LY-2795050
LY2795050;LY 2795050;LY-2795050;1346133-08-1
3-chloro-4-[4-[ [ (2S)-2-(3-pyridyl)pyrrolidin-1-yl]methyl]phenoxy]benzamide
(S)-3-chloro-4-(4-((2-(pyridin-3-yl)pyrrolidin-1-yl)methyl)phenoxy)benzamide
Benzamide, 3-chloro-4-[4-[[(2S)-2-(3-pyridinyl)-1-pyrrolidinyl]methyl]phenoxy]-
[Molecular Formula]

C23H22ClN3O2
[MOL File]

1346133-08-1.mol
[Molecular Weight]

407.89
Chemical PropertiesBack Directory
[Boiling point ]

532.4±50.0 °C(Predicted)
[density ]

1.287±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 50 mg/mL (122.58 mM; Need ultrasonic)
[form ]

Powder
[pka]

15.57±0.50(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

LY2795050 is a short-acting selective κ(kappa)-opioid receptor (KOR) antagonist. LY2795050 has high affinity for the KOR with Ki value of 0.72 nM. LY2795050 can be used for the research of central nervous system dysfunction[1][2].
[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[2].
LY2795050 (i.p., 0.032-0.1mg/kg, 0-150 min) has sexual dimorphism in some behavioral effects[2].

Animal Model:C57BL/6J mice[2]
(gonadally intact, adult, male and female)
Dosage:0.032-0.1 mg/kg
Administration:i.p., 0.032-0.1mg/kg, 30 min
Result: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.
[References]

[1] Ming-Qiang Zheng, et al. Synthesis and evaluation of 11C-LY2795050 as a κ-opioid receptor antagonist radiotracer for PET imaging. J Nucl Med DOI:10.2967/jnumed.112.109512
[2] Eduardo R Butelman, et al. Profile of a short-acting κ-antagonist, LY2795050, on self-grooming behaviors, forced swim test and locomotor activity: sex comparison in mice. J Psychopharmacol. 2021 May;35(5):579-590. DOI:10.1177/0269881121996883
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