
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥389 | 有现货 |
![]() ![]() |
5MG | ¥648 | 有现货 |
![]() ![]() |
10MG | ¥1037 | 有现货 |
![]() ![]() |
25MG | ¥2203 | 有现货 |
![]() ![]() |
50MG | ¥3467 | 有现货 |
![]() ![]() |
100MG | ¥5176 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称LY 2456302
-
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
-
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。
-
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.
-
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.
-
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.
-
同义词CERC-501 | JSPA 0658 | Aticaprant
-
通路Endocrinology/Hormones
-
靶点Opioid Receptor
-
受体Opioid Receptor
-
研究领域Neurological Disease
-
适应症Depression
化学信息
-
CAS Number1174130-61-0
-
分子量418.512
-
分子式C26H27FN2O2
-
纯度>98% (HPLC)
-
溶解度DMSO : ≥ 100 mg/mL 238.95 mM
-
SMILESO=C(N)C1=CC=C(OC2=CC=C(CN3[C@H](C4=CC(C)=CC(C)=C4)CCC3)C=C2)C(F)=C1
-
化学全称4-(4-(((2S)-2-(3,5-dimethylphenyl)-1-pyrrolidinyl)methyl)phenoxy)-3-fluoro-benzamide
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
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




关联产品
-
Trimebutine CTB salt
Trimebutine CTB salt (GIC-1001) is an opioid receptor agonist used in the study of pain.
-
BTRX-335140
BTRX-335140 是一种有效、选择性、口服活性 κ 阿片受体 (KOR) 拮抗剂,对 κOR、μOR 和 δOR 具有拮抗剂活性,IC50 值分别为 0.8 nM、110 nM 和 6500 nM。
-
LY 2456302
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。