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FTIDC 是非竞争性和选择性的口服变构代谢型谷氨酸受体 1 拮抗剂,对人 mGluR1a 的IC50为 5.8 nM。
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FTIDC 是非竞争性和选择性的口服变构代谢型谷氨酸受体 1 拮抗剂,对人 mGluR1a 的IC50为 5.8 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 917 | In stock | |
2 mg | ¥ 1,370 | In stock | |
5 mg | ¥ 2,360 | In stock | |
10 mg | ¥ 3,770 | In stock | |
25 mg | ¥ 5,930 | In stock | |
50 mg | ¥ 8,190 | In stock | |
100 mg | ¥ 10,800 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 2,530 | In stock |
FTIDC 相关产品
产品描述 | FTIDC is a highly potent and selective allosteric antagonist of mGluR1 receptors and shows very weak potency against human and rat mGluR5 receptors. The inhibition of FTIDC for mGluR1 receptors is shown to be in noncompetitive manner and displays IC50 values of 5.8 and 3.1 nM for human and mouse mGluR1 expressed in CHO cells respectively. |
靶点活性 | mGlu5:6200 nM, mGluR1(mouse):3.1 nM, mGluR1(human):5.8 nM |
分子量 | 358.41 |
分子式 | C18H23FN6O |
CAS No. | 873551-53-2 |
Smiles | CC(C)N(C)C(=O)N1CCC(=CC1)c1nnn(c1C)-c1cccnc1F |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 35.8 mg/mL (99.89 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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