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TrkA-IN-3 是一种选择性小分子抑制剂,IC50 值为 22.4 nM。TrkA-IN-3 可靶向神经生长因子受体 TrkA 的酪氨酸激酶活性,从而阻断其下游信号通路。在体外实验中,TrkA-IN-3 能够抑制 TrkA 阳性细胞的增殖和信号转导,常用于研究神经元生长、疼痛信号传递及相关肿瘤细胞的生物学机制。
别名 TrkA 抑制剂 3
TrkA-IN-3 是一种选择性小分子抑制剂,IC50 值为 22.4 nM。TrkA-IN-3 可靶向神经生长因子受体 TrkA 的酪氨酸激酶活性,从而阻断其下游信号通路。在体外实验中,TrkA-IN-3 能够抑制 TrkA 阳性细胞的增殖和信号转导,常用于研究神经元生长、疼痛信号传递及相关肿瘤细胞的生物学机制。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 1,290 | 现货 | |
| 5 mg | ¥ 2,880 | 现货 | |
| 10 mg | ¥ 4,970 | 现货 | |
| 25 mg | ¥ 7,570 | 现货 | |
| 50 mg | ¥ 9,870 | 现货 | |
| 100 mg | ¥ 13,700 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 2,970 | 现货 |
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| 产品描述 | TrkA-IN-3 is a selective small-molecule inhibitor with an IC₅₀ value of 22.4 nM. TrkA-IN-3 targets the tyrosine kinase activity of the nerve growth factor receptor TrkA, thereby blocking its downstream signaling pathways. In vitro, TrkA-IN-3 inhibits the proliferation and signal transduction of TrkA-positive cells and is commonly used to study the biological mechanisms underlying neuronal growth, pain signaling, and related tumor cells. |
| 靶点活性 | TrkA:22.4 nM |
| 别名 | TrkA 抑制剂 3 |
| 分子量 | 466.41 |
| 分子式 | C24H17F3N4O3 |
| CAS No. | 3026111-73-6 |
| Smiles | O=C(O)C1=CN=C(C=2C=CC=CC2)C(=C1)NC(=O)C=3C=CC(=C(C3)C4=NN(C=C4)C)C(F)(F)F |
| 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. 实际储存温度请以COA为准 | ||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 40 mg/mL (85.76 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。 | |||||||||||||||||||||||||||||||
对于不同动物的给药剂量换算,您也可以参考 更多