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Submit ReviewPifithrin-μ inhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL. Displays no effect on the transactivational or cell cycle checkpoint control function of p53. Potentially increases reprogramming efficiency of human somatic cells to induced pluripotent stem cells (iPSCs) by silencing p53. Pifithrin-μ reduces cell death induced by γ-radiation in vitro and protects mice from doses of radiation that cause lethal hematopoietic syndrome. Selectively inhibits heat shock protein 70 (HSP70) activity.
分子量 | 181.21 |
公式 | C8H7NO2S |
储存 | Store at +4°C |
纯度 | ≥99% (HPLC) |
CAS Number | 64984-31-2 |
PubChem ID | 327653 |
InChI Key | ZZUZYEMRHCMVTB-UHFFFAOYSA-N |
Smiles | NS(=O)(=O)C#CC1=CC=CC=C1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 13.12 | 100 | |
ethanol | 13.12 | 100 |
以下数据基于产品分子量 181.21。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 5.52 mL | 27.59 mL | 55.18 mL |
5 mM | 1.1 mL | 5.52 mL | 11.04 mL |
10 mM | 0.55 mL | 2.76 mL | 5.52 mL |
50 mM | 0.11 mL | 0.55 mL | 1.1 mL |
参考文献是支持产品生物活性的出版物。
Strom et al (2006) Small-molecule inhibitor of p53 binding to mitochondria protects mice from gamma radiation. Nat.Chem.Biol. 2 474 PMID: 16862141
Leu et al (2009) A small molecule inhibitor of inducible heat shock protein 70 (HSP70). Mol.Cell 36 15 PMID: 19818706
Kawamura et al (2009) Linking the p53 tumor suppressor pathway to somatic cell reprogramming. Nature 460 1140 PMID: 19668186
Steele et al (2009) 2-phenylacetylenesulfonamide (PAS) induces p53-independent apoptotic killing of B-chronic lymphocytic leukemia (CLL) cells. Blood 114 1217 PMID: 19515722
If you know of a relevant reference for Pifithrin-μ, please let us know.
关键词: Pifithrin-mu, Pifithrin-mu supplier, inhibitors, inhibits, p53-mitochondrial, binding, Transcription, Factors, MDM2, p14ARF, Pifithrin-mu, NSC303580, NSC, 303580, p53, Stem, Cell, Reprogramming, Hsp70, 2653, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Pifithrin-μ 的部分引用包括:
Kojima et al (2010) The novel tryptamine derivative JNJ-26854165 induces wild-type p53- and E2F1-mediated apoptosis in acute myeloid and lymphoid leukemias. Mol Cancer Ther 9 2545 PMID: 20736344
Li et al (2018) Zinc deficiency causes neural tube defects through attenuation of p53 ubiquitylation. Development 145 PMID: 30545932
Nemade et al (2018) Cell death mechanisms of the anti-cancer drug EPEG on human cardiomyocytes isolated from pluripotent stem cells. Arch Toxicol 92 1507 PMID: 29397400
Xia et al (2014) EZH2 silencing with RNA interference induces G2/M arrest in human lung cancer cells in vitro. Biomed Res Int 2014 348728 PMID: 24745014
Blatzer et al (2015) Blocking Hsp70 Enhances the Efficiency of amphote. B Treatment against Resistant Aspergillus terreus Strains. Antimicrob Agents Chemother 59 3778 PMID: 25870060
Wang et al (2013) Active Constituents from Liriope platyphylla Root against Cancer Growth In Vitro. PLoS One 2013 857929 PMID: 23762164
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Pifithrin-µ were dissolved in DMSO and used at a final concentration of 50 µM for pifithrin-µ according to previous studies in which 10-50 µM pifithrin-µ were employed.
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