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(Rac)-JBJ-04-125-02 (JBJ-04-125-02) 是 JBJ-04-125-02 的消旋体,是选择性突变,可口服的 EGFR 变构抑制剂,对EGFRL858R/T790M 的IC50为 0.26 nM。
(Rac)-JBJ-04-125-02 (JBJ-04-125-02) 是 JBJ-04-125-02 的消旋体,是选择性突变,可口服的 EGFR 变构抑制剂,对EGFRL858R/T790M 的IC50为 0.26 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 847 | In stock | |
5 mg | ¥ 2,280 | In stock | |
10 mg | ¥ 3,660 | In stock | |
25 mg | ¥ 5,890 | In stock | |
50 mg | ¥ 8,190 | In stock | |
100 mg | ¥ 10,800 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 2,730 | In stock |
(Rac)-JBJ-04-125-02 相关产品
产品描述 | (Rac)-JBJ-04-125-02 (JBJ-04-125-02) is effective as a single agent in both in vitro and in vivo models of EGFR-mutant lung cancer. |
靶点活性 | EGFR:0.26 nM |
体外活性 | (Rac)-JBJ-04-125-02为JBJ-04-125-02的外消旋体。JBJ-04-125-02是一种强效、突变选择性、变构位点特异性以及可口服的EGFR抑制剂,针对EGFRL858R/T790M的IC50为0.26 nM[1]。 |
体内活性 | Osimertinib与JBJ-04-125-02的组合,比单独使用任何一种化合物都是一种效果显著更佳的治疗方法[1]。 |
动物实验 | Ba/F3, H1975, H3255GR and H3255DR cells were treated with increasing concentrations of inhibitors for 72 hours and growth or the inhibition of growth was assessed by MTS assay according to previously established methods. |
别名 | JBJ-04-125-02 |
分子量 | 543.61 |
分子式 | C29H26FN5O3S |
CAS No. | 2140807-05-0 |
Smiles | Oc1ccc(F)cc1C(N1Cc2ccc(cc2C1=O)-c1ccc(cc1)N1CCNCC1)C(=O)Nc1nccs1 |
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: 55 mg/mL (101.18 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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