AES-350
- Product Name
- AES-350
- CAS No.
- 847249-57-4
- Chemical Name
- AES-350
- Synonyms
- AES-350;4-(4-tert-butylbenzamido)-N-hydroxybenzamide;4-[[4-(1,1-dimethylethyl)benzoyl]amino]-N-hydroxy-benzamide;Benzamide, 4-[[4-(1,1-dimethylethyl)benzoyl]amino]-N-hydroxy-;Histone deacetylases,AES 350,MV4-11,AES-350,Apoptosis,acute myeloid leukemia,AML,Inhibitor,inhibit,AES350,HDAC
- CBNumber
- CB28571007
- Molecular Formula
- C18H20N2O3
- Formula Weight
- 312.36
- MOL File
- 847249-57-4.mol
AES-350 Property
- Density
- 1.218±0.06 g/cm3(Predicted)
- storage temp.
- 4°C, protect from light
- solubility
- DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml,Ethanol: 1 mg/ml
- form
- A crystalline solid
- pka
- 8.93±0.10(Predicted)
- color
- Off-white to light yellow
AES-350 Chemical Properties,Usage,Production
Uses
AES-350 is a potent and orally active HDAC6 inhibitor with an IC50 and a Ki of 0.0244 μM and 0.035 μM, respectively. AES-350 is also against HDAC3, HDAC8 in an enzymatic activity assay with IC50 values of 0.187 μM and 0.245 μM, respectively. AES-350 triggers apoptosis in AML cells through HDAC inhibition and can be used for acute myeloid leukemia (AML) research[1].
in vivo
AES-350 (oral gavage; 20 mg/kg; single dose) exhibits a relative good pharmacokinetic (PK) properties in CD-1 mice. The single dose oral bioavailability (F%) of 51 is 19.8%. In comparison, the reported F% for SAHA in mice is significantly lower (8%)[1].
IC 50
HDAC6: 24.4 nM (IC50); HDAC3: 187 nM (IC50); HDAC11: 245 nM (IC50)
References
[1] Andrew E Shouksmith, et al. Class I/IIb-Selective HDAC Inhibitor Exhibits Oral Bioavailability and Therapeutic Efficacy in Acute Myeloid Leukemia. DOI:10.1021/acsmedchemlett.9b00471
AES-350 Preparation Products And Raw materials
Raw materials
Preparation Products
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