Name | ac-93253 iodide |
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Description | AC-93253 is a selective, potent SIRT2 inhibitor. AC93253 can inhibit SIRT2 with an IC50 value of 6 μM. AC93253 can be used for the research of tumors[1]. |
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Related Catalog | |
Target |
SIRT1:45.3 μM (IC50) SIRT2:6 μM (IC50) SIRT3:24.6 μM (IC50) |
In Vitro | AC93253 可抑制 SIRT1、SIRT2 和 SIRT3,IC50 值分别为 45.3 μM、6 μM 和 24.6 μM[1]。 AC-93253(0、2、5、10 μM;16 h)显著增强微管蛋白、p53 和组蛋白 H4 的乙酰化[1]。 AC-93253 对四种肿瘤细胞系表现出选择性细胞毒性,IC50 值范围为 10 - 100 nM[1]。 AC-93253 显著触发细胞凋亡[1]。 Western Blot Analysis[1] Cell Line: NCI-H460 cells, HeLa cells Concentration: 0, 2, 5, 10 μM Incubation Time: 16 h Result: Increased the acetylation levels of a-tubulin in a dose-dependent manner. Increased the level of histone protein and p53. |
References |
Molecular Formula | C23H25IN2S |
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Molecular Weight | 488.42700 |
Exact Mass | 488.07800 |
PSA | 35.36000 |
LogP | 2.60240 |
RIDADR | NONH for all modes of transport |
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~% 108527-83-9 |
Literature: Hamer et al. Journal of the Chemical Society, 1948 , p. 1872,887 |
Precursor 2 | |
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DownStream 0 |