Pifithrin-α 抑制剂,MDM-2/p53
| 英文名 | PIFITHRIN-ALPHA | CAS号 | 63208-82-2 |
| 产品编号 | FSY0327 | 分子式 | C16H19BrN2Os |
| 产品分类 | 化合物与抑制剂 | 分子量 | 367.30 |
| 纯度 | ≥98% (HPLC) | 储存条件 | -20℃ |
产品描述:
一种p53抑制剂,抑制p53依赖性的p53应答基因转录。
本Pifithrin-α为Pifithrin-α• hydrobromide,简称Pftα,是一种常用的p53抑制剂。Pifithrin-α能可逆性地抑制p53依赖的基因转录激活,例如cyclin G, p21/waf1和mdm2;也可以抑制p53介导的细胞凋亡。本产品为进口分装,纯度大于98%。可以用于细胞培养,也可以用于动物实验。
产品特性:
CAS NO:63208-82-2
MW:367.30
MF:C16H18N2OS·HBr,
溶解性:可溶于DMSO或甲醇。溶于DMSO(20 mg/mL)
包装:5mg 25mg 100mg in glass bottle
Pifithrin-α is a reversible inhibitor of p53-mediated apoptosis and p53-dependent gene transcription such as cyclin G, p21/waf1, and mdm2 expression. Pifithrin-α enhances cell survival after genotoxic stress such as UV irradiation and treatment with cytotoxic compounds including doxorubicin, etopoxide, paclitaxel, and cytosine-β-D-arabinofuranoside. Pifithrin-α protects mice from lethal whole body γ-irradiation without an increase in cancer incidence. The protective effect is not seen in p53-null mice or cells expressing a dominant negative mutant of the p53 gene. Protection is conferred by the transient expression of p53 in p53-deficient cell lines.