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BI-3802 能够抑制 BCL6 的Bric-à-brac (BTB) 结构域,IC50 ≤3 nM。它可诱导 BCL6 蛋白聚集,并促进 E3 连接酶SIAH1介导的蛋白降解。BI-3802显示出抗肿瘤活性。
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BI-3802 能够抑制 BCL6 的Bric-à-brac (BTB) 结构域,IC50 ≤3 nM。它可诱导 BCL6 蛋白聚集,并促进 E3 连接酶SIAH1介导的蛋白降解。BI-3802显示出抗肿瘤活性。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,260 | 现货 | |
5 mg | ¥ 2,970 | 现货 | |
10 mg | ¥ 4,390 | 现货 | |
25 mg | ¥ 6,870 | 现货 | |
50 mg | ¥ 9,460 | 现货 | |
100 mg | ¥ 12,700 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 2,990 | 现货 |
产品描述 | BI-3802, a highly potent BCL6 degrader, targets and inhibits the Bric-à-brac (BTB) domain of BCL6, exhibiting an IC50 value of ≤3 nM. It induces polymerization of BCL6 and facilitates its degradation in a manner dependent on the E3 ligase SIAH1, demonstrating notable antitumor activity[1][2]. |
靶点活性 | BCL6 BTB:≤ 3 nM |
体外活性 | BI-3802 对细胞内BCL6展现了43 nM的IC50值[1]。BI-3802促进了BCL6与SIAH1之间的相互作用(EC50 = 64 nM)[2]。 |
分子量 | 484.98 |
分子式 | C24H29ClN6O3 |
CAS No. | 2166387-65-9 |
Smiles | CNC(=O)COc1cc2cc(Nc3nc(ncc3Cl)N3C[C@@H](C)C[C@@H](C)C3)ccc2n(C)c1=O |
密度 | 1.35 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||
溶解度信息 | DMSO: 5 mg/mL (10.31 mM), Sonication is recommended. | ||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||
DMSO
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