化合物SU16f T16947
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 |
---|---|---|---|
25 mg | 251356-45-3 | ¥1,190.00 | 询底价 |
1 mL | 251356-45-3 | ¥525.00 | 询底价 |
1 mg | 251356-45-3 | ¥237.00 | 询底价 |
50 mg | 251356-45-3 | ¥1,780.00 | 询底价 |
10 mg | 251356-45-3 | ¥696.00 | 询底价 |
5 mg | 251356-45-3 | ¥475.00 | 询底价 |
100 mg | 251356-45-3 | ¥2,610.00 | 询底价 |
Product Introduction
Bioactivity
英文名: SU16f
描述: SU16f (3-substituted indolin-2-one 16f) 是一种有效的,选择性 PDGFRβ 抑制剂,对 PDGFRβ,PDGFR1,PDGFR2 的 IC50 分别为 10 nM,140 nM,2.29 μM。SU16f 抑制 PDGFRβ 受体从而可以阻断胃癌来源的间充质干细胞 (GC-MSC) 条件培养基在胃癌细胞增殖和迁移中的促进作用。
体外活性: SU16f (20 μM; for 8 hours) significantly abolishes PDGFRβ activation in SGC-7901 by GC-MSC-CM. SU16f (20 μM; for 8 hours) pretreatment inhibits the promoting role of GC-MSC-CM in SGC-7901 cell proliferation. SU16f pretreatment leads to downregulation of p-AKT, Bcl-xl, and Bcl-2 levels and upregulation of Bax expression in SGC-7901 cells by GC-MSC-CM. SU16f pretreatment causes the upregulation of E-cadherin and downregulation of N-cadherin, Vimentin, and α-SMA [1].
存储条件: store at low temperaturePowder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 25 mg/mL (64.69 mM)
关键字: SU16f
相关产品: Sennoside B | 5Z-7-Oxozeaenol | Ilorasertib | Sunitinib Malate | Sorafenib tosylate | JI-101 | Seralutinib | GZD856 | Lenvatinib mesylate | Ponatinib
相关库: PDGFR inhibitor kit | Anti-Cancer Compound Library | Membrane Protein-targeted Compound Library | Anti-Lung Cancer Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Kinase Inhibitor Library | Tyrosine Kinase Inhibitor Library | Anti-Cancer Active 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