LY-2795050
- Product Name
- LY-2795050
- CAS No.
- 1346133-08-1
- Chemical Name
- LY-2795050
- Synonyms
- LY2795050;LY-2795050;LY 2795050;LY 2795050; LY-2795050;LY2795050, 10 mM in DMSO;LY2795050;LY 2795050;LY-2795050;1346133-08-1;(S)-3-chloro-4-(4-((2-(pyridin-3-yl)pyrrolidin-1-yl)methyl)phenoxy)benzamide;3-chloro-4-[4-[ [ (2S)-2-(3-pyridyl)pyrrolidin-1-yl]methyl]phenoxy]benzamide;3-chloro-4-(4-{[(2S)-2-(pyridin-3-yl)pyrrolidin-1-yl]methyl}phenoxy)benzamide;Benzamide, 3-chloro-4-[4-[[(2S)-2-(3-pyridinyl)-1-pyrrolidinyl]methyl]phenoxy]-
- CBNumber
- CB42666653
- Molecular Formula
- C23H22ClN3O2
- Formula Weight
- 407.89
- MOL File
- 1346133-08-1.mol
LY-2795050 Property
- 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
N-Bromosuccinimide Price
- Product number
- CS-1519
- Product name
- LY2795050
- Purity
- 98.12%
- Packaging
- 5mg
- Price
- $240
- Updated
- 2021/12/16
- Product number
- CS-1519
- Product name
- LY2795050
- Purity
- 98.12%
- Packaging
- 10mg
- Price
- $384
- Updated
- 2021/12/16
- Product number
- CS-1519
- Product name
- LY2795050
- Purity
- 98.12%
- Packaging
- 50mg
- Price
- $900
- Updated
- 2021/12/16
- Product number
- CS-1519
- Product name
- LY2795050
- Purity
- 98.12%
- Packaging
- 100mg
- Price
- $1680
- Updated
- 2021/12/16
- Product number
- DC10815
- Product name
- LY2795050
- Purity
- >98%
- Packaging
- 1g
- Price
- $2600
- Updated
- 2021/12/16
LY-2795050 Chemical Properties,Usage,Production
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
LY-2795050 Preparation Products And Raw materials
Raw materials
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