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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
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 Number
    1174130-61-0
  • 分子量
    418.512
  • 分子式
    C26H27FN2O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 100 mg/mL 238.95 mM
  • SMILES
    O=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
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    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。