| 名称 | MC1568 |
| 描述 | MC1568 is a specific HDAC inhibitor for maize HD1-A (IC50: 100 nM, in a cell-free assay). It is 34-fold more selective for HD1-A than HD1-B. |
| 细胞实验 | The 3T3-L1 cells are propagated and differentiated using a cocktail of isobutylmethylxanthine, dexamethasone, and insulin. From the second day post-confluence and throughout the differentiation period of 8 days, the 3T3-L1 cells are induced by: (1) no induction: at post-confluence and throughout the differentiation period of 8 days, the cells are incubated with DMSO or MC1568. (2) troglitazone: at post-confluence and throughout the differentiation period of 8 days, the cells are induced with 5 μM troglitazone, MC1568, or both. (3) rosiglitazone: at post-confluence and throughout the differentiation period of 8 days, the cells are incubated with 1?μM rosiglitazone and either DMSO or MC1568. (4) rosiglitazone and dexamethasone: at post-confluence, the cells received 1?μM of rosiglitazone and 390?ng/mL dexamethasone. Throughout the differentiation period of 8 days, the cells are induced with 1?μM of rosiglitazone and either DMSO or MC1568. All medium is renewed every second day.(Only for Reference) |
| 激酶实验 | Maize HD2, HD1-B, and HD1-A Enzyme Inhibition.: The enzyme liberats tritiated acetic acid from the substrate, which is quantified by scintillation counting. IC50 values are results of triple determinations. A 50 μL sample of maize enzyme (at 30 °C) is incubated (30 min) with 10 μL of total [3H]acetate-prelabeled chicken reticulocyte histones (2 mg/mL). Reaction is stopped by addition of 50 μL of 1 M HCl/0.4 M acetate and 800 μL of ethyl acetate. After centrifugation (1×104 g, 5 min), an aliquot of 600 μL of the upper phase is counted for radioactivity in 3 mL of liquid scintillation cocktail. MC1568 is tested at a starting concentration of 40 μM, and active substances are diluted further. NaB, VPA, TSA, SAHA, 85 TPX, HC-toxin, and tubacin are used as the reference compounds, and blank solvents are used as negative controls. |
| 体外活性 | 在胰脏移植研究中,MC1568增强内分泌β和δ-cells细胞,并使Pax4的表达增强. 在鼠体内,MC1568（50 mg/kg）组织选择性地显著抑制HDAC. 在PPRE-Luc鼠体内,MC1568（50 mg/kg）主要损害心脏和脂肪组织部位PPARγ信号.作用于骨骼肌和心脏时,MC1568抑制HDAC4/5的活性,不影响HDAC3活性,故MEF2-HDAC复合体处于未激活状态. |
| 体内活性 | MC1568对HDAC II的选择性抑制效果（IC50：220 nM）是I型的176倍。作用于C2C12细胞时,MC1568（5 μM）通过降低肌细胞增强因子2D的表达,使HDAC4-HDAC3-MEF2D复合体稳定,并抑制分化诱导的MEF2D乙酰化,从而使肌细胞生成被阻断。MC1568（5或10 μM）可使RAR和PPARγ调节的分化诱导信号通路受干扰。 在MCF-7细胞中,MC1568（20 μM）使乙酰化H3和H4组蛋白的累积增强,并提高乙酰基微管蛋白的水平,表明MC1568可抑制HDAC6。作用于人类乳腺癌ZR-75.1细胞裂解物时,MC1568对HDAC1无抑制作用,但是可使HDAC4受抑制。作用于F9细胞时,MC1568选择性抑制内胚分化,对VA诱导的早幼粒NB4细胞成熟无影响。作用于3T3-L1细胞时,MC1568使PPARγ诱导的脂肪生成降低。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | H2O : < 1 mg/mL (insoluble or slightly soluble)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 11 mg/mL (35 mM), Sonication is recommended.
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| 关键字 | MC-1568 | MC1568 | MC 1568 | Inhibitor | inhibit | Histone deacetylases | HDAC | HD1-B (Maize) | HD1-A (Maize) |
| 相关产品 | Valproic acid sodium salt | 4-Phenylbutyric acid | Valproic Acid | Sodium butanoate | Panobinostat | Manganese chloride (tetrahydrate) | Methoxyacetic acid | Theophylline | Acefylline | Curcumin | Theophylline monohydrate | Sodium 4-phenylbutyrate |
| 相关库 | 抑制剂库 | 抗乳腺癌化合物库 | 经典已知活性库 | 抗癌化合物库 | 已知活性化合物库 | 自噬库 | 抗胰腺癌化合物库 | 组蛋白修饰化合物库 | 抗衰老化合物库 | HIF-1化合物库 | 血液病分子库 | 细胞重编程化合物库 |