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LY2795050 Sale

目录号 : GC19500

A κ-opioid receptor antagonist

LY2795050  Chemical Structure

Cas No.:1346133-08-1

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥1,752.00
现货
2mg
¥1,302.00
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5mg
¥1,953.00
现货
10mg
¥2,968.00
现货
50mg
¥7,031.00
现货
100mg
¥10,937.00
现货

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Sample solution is provided at 25 µL, 10mM.

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LY2795050 is a novel selective κ-opioid Receptor (KOR) antagonist (IC50=0.72 nM) and has the potential as a PET tracer to image KOR in vivo. IC50 Value: 0.72 nM (κ-opioid Receptor); 25.8 nM (κ-opioid) [1] Target: κ-opioid Receptor in vitro: LY2795050 displays full antagonist activity and high binding affinity and selectivity for KOR with a ki value of 0.72 nM [1]. in vivo: In the brain, (11)C-LY2795050 displayed fast uptake kinetics (regional activity peak times of <20 min) and an uptake pattern consistent with the distribution of KOR in primates [1]. The LY2795050 ED50 at MOR was 119 μg/kg based on a 1-site model for 11C-carfentanil. The 1-site binding model was also deemed sufficient to describe the specific binding of 11C-LY2795050 at KOR. The ED50 at KOR estimated from the 1-site model was 15.6 μg/kg. Thus, the ED50 ratio for MOR:KOR was 7.6 [2].

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.
[2]. Zheng MQ, Nabulsi N, Kim SJ, Synthesis and evaluation of 11C-LY2795050 as a κ-opioid receptor antagonist radiotracer for PET imaging. J Nucl Med. 2013 Mar;54(3):455-63.
[3]. Kim SJ, Zheng MQ, Nabulsi N, Determination of the In Vivo Selectivity of a New κ-Opioid Receptor Antagonist PET Tracer 11C-LY2795050 in the Rhesus Monkey. J Nucl Med. 2013 Aug 5.

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1 mg 5 mg 10 mg
1 mM 2.4516 mL 12.2582 mL 24.5164 mL
5 mM 0.4903 mL 2.4516 mL 4.9033 mL
10 mM 0.2452 mL 1.2258 mL 2.4516 mL
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