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ADX88178

CAS No. 1235318-89-4

ADX88178 ( ADX-88178 | ADX 88178 | ADX88178 )

产品货号. M17210 CAS No. 1235318-89-4

ADX88178 是代谢型谷氨酸受体 4 (mGluR4) 的有效正变构调节剂,对人 mGluR4 的 EC50 为 4 nM。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥437 有现货
5MG ¥721 有现货
10MG ¥1191 有现货
25MG ¥2130 有现货
50MG ¥3443 有现货
100MG ¥5046 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
    ADX88178
  • 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
    ADX88178 是代谢型谷氨酸受体 4 (mGluR4) 的有效正变构调节剂,对人 mGluR4 的 EC50 为 4 nM。
  • 产品描述
    ADX-88178 is a novel potent, selective, and brain-penetrant positive allosteric modulator of the mGlu4 receptor in rodent models of anxiety, obsessive compulsive disorder (OCD), fear, depression, and psychosis. ADX88178 dose-dependently reduced the number of buried marbles in the marble burying test and increased open-arm exploration in the elevated plus maze (EPM) test, indicative of anxiolytic-like efficacy.
  • 体外实验
    ADX88178 is developed as a potent and selective mGluR4 positive allosteric modulator. ADX88178 is used as a novel radioligand for imaging of metabotropic glutamate receptor subtype 4 (mGluR4). ADX88178 potentiates glutamate-mediated activation of human mGluR4 with EC50 values of 4 nM without significant effects on other mGluRs (EC50 > 30 μM). ADX88178 is novel potent, selective, and brain-penetrant positive allosteric modulator of the mGlu4.Microglia are pretreated with 1, 10 or 100 nM ADX88178 or 100 nM LAP4 for 30 min followed by LPS treatment for 24 h prior to collecting culture supernatant for ELISA measurement of TNFα levels. The pre-treatment with ADX88178 and LAP4 both significantly attenuate LPS-induced TNFα levels. As little as 1 nM of ADX88178 is sufficient to inhibit TNFα, and is as effective at concentrations of 10 and 100 nM.
  • 体内实验
    In mice, ADX88178 (1-30 mg/kg p.o.) dose-dependently increases the number of open-arm entries. Specifically, at 3, 10, and 30 mg/kg ADX88178, there are 5-, 7-, and almost 13-fold increases in the number of open-arm entries, respectively, when compared with the vehicle-treated controls. Also, ADX88178 dose-dependently increases the time spent in the open arms. Specifically, at 3, 10, and 30 mg/kg ADX88178, there are 8-, 12-, and 24-fold increases in the time spent in the open arms when compared with the vehicle-treated controls. In rats, ADX88178 (10-100 mg/kg p.o.) dose-dependently increases the number of open-arm entries in the rat EPM test. Specifically, at 10, 30, and 100 mg/kg ADX88178, there are 5-, 8-, and more than 10-fold increases in the number of open-arm entries, respectively, when compared with the vehicle-treated controls. Also, ADX88178 dose-dependently increases the time spent in the open arms. Specifically, at 10, 30, and 100 mg/kg ADX88178, there are 7.5-, 11-, and 13-fold increases in time spent in the open arms when compared with the vehicle-treated controls.
  • 同义词
    ADX-88178 | ADX 88178 | ADX88178
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    human mGluR4
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1235318-89-4
  • 分子量
    272.33
  • 分子式
    C12H12N6S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 50 mg/mL 183.60 mM
  • SMILES
    Cc1nc(Nc2nc(c3c[nH]nc3)c(C)s2)ncc1
  • 化学全称
    5-methyl-N-(4-methylpyrimidin-2-yl)-4-(1H-pyrazol-4-yl)thiazol-2-amine

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. Fujinaga M, et al. Bioorg Med Chem Lett. 2016 Jan 15;26(2):370-4.
产品手册
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