LY 2456302
CAS No. 1174130-61-0
LY 2456302 ( CERC-501 | JSPA 0658 | Aticaprant )
产品货号. M10590 CAS No. 1174130-61-0
LY 2456302 (CERC-501, JSPA 0658, Aticaprant) 是一种有效、选择性、短效的 κ-阿片受体 (KOR) 拮抗剂,Ki 为 0.81 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥708 | 有现货 |
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| 10MG | ¥1093 | 有现货 |
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| 25MG | ¥1823 | 有现货 |
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| 50MG | ¥2911 | 有现货 |
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| 100MG | ¥4041 | 有现货 |
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| 200MG | ¥5697 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥777 | 有现货 |
|
生物学信息
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产品名称LY 2456302
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述LY 2456302 (CERC-501, JSPA 0658, Aticaprant) 是一种有效、选择性、短效的 κ-阿片受体 (KOR) 拮抗剂,Ki 为 0.81 nM。
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产品描述LY 2456302 (CERC-501, JSPA 0658, Aticaprant) is a potent, selective, short-acting antagonist of κ-opioid receptor (KOR) with Ki of 0.81 nM; displays >30-fold selectivity over MOR and DOR; selectively and potently occupies central kappa opioid receptors in vivo (ED50=0.33 mg/kg); produces antidepressant-like effects in the mouse forced swim test and enhanced the effects of imipramine and citalopram; orally-bioavailable and excellent pharmacokinetic properties.Depression Phase 2 Clinical.
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体外实验Aticaprant (CERC-501) binds with high affinity to the human kappa opioid receptor with a 30-fold higher affinity over the human mu opioid receptor and 190-fold higher affinity over the human delta opioid receptor. Aticaprant (CERC-501) shows no appreciable affinity for several non-opioid cell surface G-protein-coupled receptor targets, including monoaminergic, muscarinic, cholinergic, and adrenergic receptors or ion channel/transporter binding targets or the central benzodiazepine binding site.
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体内实验Aticaprant (CERC-501) has a rapid absorption (tmax=1-2 h) and good oral bioavailability (F=25%). Oral Aticaprant (CERC-501) administration selectively and potently occupies central kappa opioid receptors (ED50=0.33 mg/kg), without evidence of mu or delta receptor occupancy. LY2456302 potently blocks kappa-agonist-mediated analgesia and disruption of prepulse inhibition, without affecting mu-agonist-mediated effects at doses >30-fold higher. Aticaprant (CERC-501) produces antidepressant-like effects in the mouse forced swim test and enhances the effects of imipramine and citalopram. Aticaprant (CERC-501) reduces ethanol self-administration in alcohol-preferring rats. Aticaprant (CERC-501) alleviates the nicotine withdrawal syndrome, as evidenced by decreased expression of nicotine withdrawal induced anxiety-related behavior, somatic signs, and CPA, and increased hotplate latency in nicotine withdrawn mice following pre-treatment.
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同义词CERC-501 | JSPA 0658 | Aticaprant
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通路Endocrinology/Hormones
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靶点Opioid Receptor
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受体Opioid Receptor
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研究领域Neurological Disease
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适应症Depression
化学信息
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CAS Number1174130-61-0
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分子量418.512
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分子式C26H27FN2O2
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 100 mg/mL 238.95 mM
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SMILESO=C(N)C1=CC=C(OC2=CC=C(CN3[C@H](C4=CC(C)=CC(C)=C4)CCC3)C=C2)C(F)=C1
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化学全称4-(4-(((2S)-2-(3,5-dimethylphenyl)-1-pyrrolidinyl)methyl)phenoxy)-3-fluoro-benzamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Rorick-Kehn LM, et al. Neuropharmacology. 2014 Feb;77:131-44.
2. Jackson KJ, et al. Neuropharmacology. 2015 Oct;97:270-4.
3. Naganawa M, et al. J Pharmacol Exp Ther. 2016 Feb;356(2):260-6.
产品手册
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