英文名:2-[2-Chloro-4-[(1,5-dihydro-3-methyl-5-oxo-1-pheny
外观:
纯度:请咨询卖家
分子式:C22H21ClN2O5
分子量:428.87
最小起售量:10g/20g/100g/1kg
中文同义词:
MDMX小分子抑制剂(SJ-172550);化合物SJ-172550
英文名称:
2-[2-Chloro-4-[(1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene)methyl]-6-ethoxyphenoxy]aceticacidmethylester
英文同义词:
2-[2-Chloro-4-[(1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene)methyl]-6-ethoxyphenoxy]aceticacidmethylester;SJ 172550;MDMX Antagonist, SJ-172550;CS-1226;MDMX Antagonist, SJ-172550 - CAS 431979-47-4 - Calbiochem;Acetic acid, 2-[2-chloro-4-[(1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene)methyl]-6-ethoxyphenoxy]-, methyl ester
沸点
560.8±60.0 °C(Predicted)
密度
1.27±0.1 g/cm3(Predicted)
酸度系数(pKa)
-0.30±0.40(Predicted)
生物活性
SJ-172550是MDMX的小分子抑制剂; 与野生型p53肽竞争性结合于MDMX的EC50值为5 μM。
体外研究
The p53 pathway is disrupted in virtually every human tumor. SJ-172550 binds the p53-binding pocket of MDMX, thereby displacing p53. SJ-172550 binds reversibly to MDMX and effectively kills retinoblastoma cells in which the expression of MDMX is amplified. The effect of SJ-172550 is additive when combined with an MDM2 inhibitor nutlin-3a. SJ-172550 acts through a complicated mechanism in which the compound forms a covalent but reversible complex with MDMX and locks MDMX into a conformation that is unable to bind p53. The relative stability of this complex is influenced by many factors including the reducing potential of the media, the presence of aggregates.