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 |
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| 5MG | ¥721 | 有现货 |
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| 10MG | ¥1191 | 有现货 |
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| 25MG | ¥2130 | 有现货 |
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| 50MG | ¥3443 | 有现货 |
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| 100MG | ¥5046 | 有现货 |
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| 200MG | 获取报价 | 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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生物学信息
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产品名称ADX88178
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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。
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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.
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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.
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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.
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同义词ADX-88178 | ADX 88178 | ADX88178
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通路Others
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靶点Other Targets
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受体human mGluR4
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研究领域——
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适应症——
化学信息
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CAS Number1235318-89-4
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分子量272.33
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分子式C12H12N6S
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 50 mg/mL 183.60 mM
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SMILESCc1nc(Nc2nc(c3c[nH]nc3)c(C)s2)ncc1
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化学全称5-methyl-N-(4-methylpyrimidin-2-yl)-4-(1H-pyrazol-4-yl)thiazol-2-amine
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. Fujinaga M, et al. Bioorg Med Chem Lett. 2016 Jan 15;26(2):370-4.
产品手册
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