Nexturastat A

CAS号

1403783-31-2

分子式

C19H23N3O3

主要靶点

HDAC

仅限科研使用

Cat No : CM04417

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Synonyms

inhibit|HDAC|HDAC6|Histone deacetylases|Nexturastat A|Inhibitor



产品信息

CAS号 1403783-31-2
分子式 C19H23N3O3
主要靶点 HDAC
主要通路 表观遗传|DNA 损伤和修复
分子量 341.4
纯度 99.57%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
别名 inhibit|HDAC|HDAC6|Histone deacetylases|Nexturastat A|Inhibitor

靶点活性

HDAC6:5 nM

体内活性

Nexturastat A对B16鼠黑色素瘤细胞的生长有显著抑制作用(GI50:14.3 μM)。在B16鼠黑色素瘤细胞中,Nexturastat A剂量依赖性增加乙酰化的α-微管蛋白水平,但不影响组蛋白H3乙酰化伴随的脓肿。

溶解度

Ethanol:2 mg/mL (5.85 mM);H2O:< 1 mg/mL (insoluble or slightly soluble);DMSO:63 mg/mL (184.5 mM)

细胞实验

B16 murine melanoma cells are plated at 5000/well in 96 well flat bottom plates. The following day, media is changed to that containing various concentrations of HDACi or matched DMSO vehicle concentrations diluted in complete medium done in triplicate. Cells are incubated for 48 hours at 37°C and 5% CO2. Density of viable, metabolically active cells is quantified using a standard MTS assay as per manufacturer’s instructions. Briefly, 20μL of reagent are added per well and incubated at 37°C for 3 hours. Absorbances at 490 nM are measured spectrophotometrically with background subtraction at 690 nM. All values are then normalized and expressed as a percentage of medium control (100%). (Only for Reference)

参考文献

1.Bergman JA, et al. J Med Chem. 2012, 55(22), 9891-9899.

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