| CAS: | 79756-69-7 | |
| 分子式: | C12H6Cl2O2 | |
| 分子量: | 253.08 | |
| 英文名称: |
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| 用途: | TPI-1是SHP-1的抑制剂;抑制重组SHP-1的IC50值为40 nM。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||
| T877331 | MACKLIN | TPI-1 | ≥98% | 154元/5mg; 263元/10mg; | 咨询 | ||||||||||||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||||||||||||
| T792546 | MACKLIN | TPI-1 | 10mM in DMSO | 909元/1ml; | 咨询 | ||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||
| SML3119 | Sigma-Aldrich | SHP1 Inhibitor, TPI-1 | ≥98% (HPLC) | 1076.74元/5 MG; 4337.05元/25 MG; | 咨询 | ||||||||||||||||||||||||||||||
产品说明 生化/生理作用 TPI-1 is an orally bioavailable, noncytotoxic benzoquinone compound that acts as a potent irreversible inhibitor of SHP-1 (Src homology region 2 domain-containing phosphatase 1) catalytic domain (IC50 ~ 40 nM or 0.01 μg/ml) with selectivity over SHP-2 (IC50 ~ 0.1 μg/ml), MKP1 (IC50 > 1 μg/ml) and CD45. TPI-1 potently induces mouse and human primary IFN-g+ cells both in vitro and in vivo. Effectively inhibits B16 melanoma tumors in mice (1 or 3 mg/kg, s.c., daily) and prolong the survival. TPI-1 is shown to be 50-fold more effective than sodium stibogluconate in cell-based assays and may non-specifically react with cysteine residues. 基本信息
产品性质
安全信息
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