ACY-957

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Chemical Structure| 1609389-52-7 同义名 : HDAC Inhibitor C001
CAS号 : 1609389-52-7
货号 : A792202
分子式 : C24H23N5OS
纯度 : 99%
分子量 : 429.537
MDL号 : MFCD30342405
存储条件:

Pure form Keep in dark place,Sealed in dry,2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 85 mg/mL(197.89 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 HDAC inhibitor C001 is an inhibitor of HDACs with IC50 of 4 nM (HDAC1), 15 nM (HDAC2), 114 nM (HDAC3), and can increase Gata2 expression, which may be useful in treatment of Gata2-deficiency-associated diseases, including leukemia and other blood cell disorders.
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.33mL

0.47mL

0.23mL

11.64mL

2.33mL

1.16mL

23.28mL

4.66mL

2.33mL

参考文献

[1]Shearstone JR, Golonzhka O, Chonkar A, Tamang D, van Duzer JH, Jones SS, Jarpe MB. Chemical Inhibition of Histone Deacetylases 1 and 2 Induces Fetal Hemoglobin through Activation of GATA2. PLoS One. 2016 Apr 13;11(4):e0153767. doi: 10.1371/journal.pone.0153767. PMID: 27073918; PMCID: PMC4830539.

[2]Mehraei M, Bashirov R, Tüzmen Ş. Target-based drug discovery for [Formula: see text]-globin disorders: drug target prediction using quantitative modeling with hybrid functional Petri nets. J Bioinform Comput Biol. 2016 Oct;14(5):1650026. doi: 10.1142/S0219720016500268. Epub 2016 Jun 21. PMID: 27431020.