化合物BPR1J-097 hydrochloride T4261
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 |
---|---|---|---|
100 mg | T4261 | ¥5,490.00 | 询底价 |
25 mg | T4261 | ¥2,580.00 | 询底价 |
50 mg | T4261 | ¥3,830.00 | 询底价 |
10 mg | T4261 | ¥1,530.00 | 询底价 |
1 mL | T4261 | ¥1,190.00 | 询底价 |
1 mg | T4261 | ¥322.00 | 询底价 |
2 mg | T4261 | ¥580.00 | 询底价 |
5 mg | T4261 | ¥935.00 | 询底价 |
Product Introduction
Bioactivity
英文名: BPR1J-097 hydrochloride (1327167-19-0(free base))
描述: BPR1J-097 hydrochloride (1327167-19-0(free base)) 是一种新型小分子 FLT-3抑制剂(IC50=11±7 nM),具有很好的体内抗肿瘤活性。
激酶实验: Cells are treated with THZ531 for 6 hours.After treatment cells are washed 2-fold with cold PBS and then lysed in the following lysis buffer: Hepes(50 mM, pH 7.4), NaCl(150 mM), 1% Nonidet P40 substitute, EDTA(5 mM), DTT(1 mM), and protease/phosphatase cocktails.Lysates are treated with bio-THZ1 or bio-TH531 for pulldown overnight at 4°C.
体内活性: In FLT3-driven AML murine xenograft models, BPR1J-097 inhibited FLT3/signal transducer and activator of transcription 5 phosphorylation and triggered apoptosis in FLT3-driven AML cells and pronounced dose-dependent tumour growth inhibition and regression.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 5.53 mg/mL (10 mM)
关键字: BPR1J 097 hydrochloride (1327167 19 0(free base)) | BPR1J-097 hydrochloride (1327167-19-0(free base)) | BPR-1J-097 hydrochloride (1327167-19-0(free base)) | BPR1J097 hydrochloride (1327167190(free base))
相关产品: BRD7389 | BPR1K871 | KW-2449 | TCS 359 | NVP-AEW541 | TG-89 | FLT3-IN-3 | UNC2025 2HCl (1429881-91-3(free base)) | Tyrphostin AG1296 | R406
相关库: Anti-Cancer Compound Library | Angiogenesis related Compound Library | Anti-Lung Cancer Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Kinase Inhibitor Library | Anti-Cancer Active Compound Library | Tyrosine Kinase Inhibitor 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