化合物TJ191 T9104
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
10 mg | 1522415-97-9 | ¥997.00 | 询底价 |
1 mg | 1522415-97-9 | ¥283.00 | 询底价 |
5 mg | 1522415-97-9 | ¥663.00 | 询底价 |
50 mg | 1522415-97-9 | ¥3,320.00 | 询底价 |
2 mg | 1522415-97-9 | ¥395.00 | 询底价 |
100 mg | 1522415-97-9 | ¥4,890.00 | 询底价 |
25 mg | 1522415-97-9 | ¥1,980.00 | 询底价 |
1 mL | 1522415-97-9 | ¥628.00 | 询底价 |
500 mg | 1522415-97-9 | ¥9,870.00 | 询底价 |
Product Introduction
Bioactivity
英文名: TJ191
描述: TJ191 是一种选择性抗癌试剂,靶向低 TβRIII 表达的恶性T 细胞白血病/淋巴瘤细胞,可研究癌症。
体外活性: TJ191 (0.1-3 μM; 8 or 24 hours) induces CEM cell apoptosis in a concentration- and time-dependent manner. Even at 0.3 μM, TJ191 induces the maximum apoptotic rate of 80% after 24 h.?TJ191(0-100 μM; 24 hours) exhibits pronounced anti-proliferative activity in malignant cell lines, the IC50 values are 0.13 μM, 0.13±0.08 μM, 0.26±0.19 μM, 0.22±0.11 μM, 1.5±0.02 μM, 0.32±0.086 μM, 3.1±0.5 μM, 0.26±0.16 μM in CEM, JURKAT, MOLT-3, MOLT-4, SUP-T1, MT-2, C8166 and HSB-2 cells, respectively. But has no effects in HUT-78 (IC50=17±10 μM) and MT-4 (IC50=47 ± 5 μM) cells.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 55 mg/mL (215.37 mM)
关键字: cancer | Apoptosis | PMBC | MOLT-3 | CEM | inhibit | C8166 | Inhibitor | MOLT-4 | MT-2 | TJ 191 | TJ-191 | TJ191 | HSB-2 | SUP-T1 | JURKAT
相关产品: PD168393 | TVB-3166 | Bendamustine | Talampanel | MYCMI-6 | DCH36_06 | Tetrahydroxyquinone | Quercetin | Dehydrocrenatidine | Vatalanib dihydrochloride
相关库: Anti-Cancer Compound Library | Bioactive Compounds Library Max | Anti-Cancer Active Compound Library | Hematonosis Compound Library | Apoptosis Compound Library | NO PAINS Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途