中文名 | BRD73954 |
英文名 | BRD73954 |
别名 | HDAC抑制剂(BRD73954) N1-羟基-N3-(2-苯基乙基)-1,3-苯二甲酰胺 |
英文别名 | CS-1777 BRD73954 BRD-73954 BRD 73954 N1-hydroxy-N3-phenethylisophthalamide N1-Hydroxy-N3-(2-phenylethyl)-1,3-benzenedicarboxamide 1,3-Benzenedicarboxamide, N1-hydroxy-N3-(2-phenylethyl)- BRD73954, 1-N-hydroxy-3-N-(2-phenylethyl)benzene-1,3-dicarboxamide N1-hydroxy-N3-(2-phenylethyl)-1,3-benzenedicarboxamide BRD73954 |
CAS | 1440209-96-0 |
化学式 | C16H16N2O3 |
分子量 | 284.31 |
密度 | 1.245±0.06 g/cm3(Predicted) |
熔点 | 172-175oC |
溶解度 | DMSO (微溶) 、甲醇 (微溶) |
酸度系数 | 8.56±0.10(Predicted) |
存储条件 | under inert gas (nitrogen or Argon) at 2-8°C |
外观 | 固体 |
颜色 | Off-White |
体外研究 | As compared to the other class I and II histone deacetylases (HDACs) (HDAC1, 12 μM; HDAC2, 9 μM; HDAC3, 23μM; HDAC4, >33 μM; HDAC5, >33 μM; HDAC7, 13 μM; HDAC8, 120 nM; HDAC9, >33 μM), BRD73954 maintains excellent selectivity toward HDAC6 and HDAC8 with IC50 of 36 nM and 120 nM, respectively. Treatment with BRD73954 results in a robust increase in α -tubulin acetylation. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.517 ml | 17.586 ml | 35.173 ml |
5 mM | 0.703 ml | 3.517 ml | 7.035 ml |
10 mM | 0.352 ml | 1.759 ml | 3.517 ml |
5 mM | 0.07 ml | 0.352 ml | 0.703 ml |
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