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AES-350

CAS No. : 847249-57-4

MCE 站：AES-350

产品活性：AES-350 是一种有效的口服活性 HDAC6 抑制剂，IC₅₀ 和 K_i 分别为 0.0244 μM 和 0.035 μM。AES-350 对 HDAC-3、-8 和 -11 的 IC₅₀ 值分别为 0.187 μM、0.245 μM 和 >1 μM。AES-350 通过抑制 HDAC 诱导 AML 细胞凋亡，可用于急性髓系白血病 (AML) 研究。

研究领域：Cell Cycle/DNA Damage  |  Epigenetics

作用靶点：HDAC

In Vitro: In contrast, AES-350 has submicromolar activity (IC₅₀=0.58±0.13 μM) against MV4-11 cells than to that of vorinostat (IC₅₀=0.31±0.061 μM). AES-350 is more ligand efficient and exemplifies a large therapeutic index (IC₅₀>30 μM in noncancerous MRC-9 cells). AES-350 is also shown to be effective in AML-3 (acute myeloid leukemia) cells (IC₅₀=0.73 ± 0.12 μM).
AES-350 (0.25-4 μM; 18 hours) induces MV4-11 cells apoptosis in a dose-dependent manner. The late apoptosis ratios are 8.74%, 11.7%,16.08%, 30.97%, and 38.48%, respectively at 0.25 μM-4 μM.
An ELISA is performed using HeLa cervical cancer cell lysates, and HeLa cells highly express HDAC6 and are sensitive to AES-350. Correspondingly, ELISA assays depicted a dose-dependent increase in HDAC6 inhibition (IC₅₀=0.58±0.13 μM), Western blot analysis shows that AES-350 (0.1-10 μM) induces a dose-dependent increase in acetylated α-tubulin (Ac-α-tubulin), a substrate of HDAC.

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%).

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