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Thiomyristoyl 是一种高效特异性SIRT2抑制剂,IC50值为28 nM。


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Thiomyristoyl 是一种高效特异性SIRT2抑制剂,IC50值为28 nM。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 611 | In Stock | |
| 2 mg | ¥ 886 | In Stock | |
| 5 mg | ¥ 1,530 | In Stock | |
| 10 mg | ¥ 2,430 | In Stock | |
| 25 mg | ¥ 4,120 | In Stock | |
| 50 mg | ¥ 5,870 | In Stock | |
| 100 mg | ¥ 8,150 | In Stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,970 | In Stock |
Thiomyristoyl 相关产品
| 产品描述 | Thiomyristoyl is an effective and selective SIRT2 inhibitor (IC50: 28 nM). It inhibits SIRT1 (IC50: 98 μM) but no effect on SIRT3 even at 200 μM. |
| 靶点活性 | SIRT1:98 μM, SIRT2:28 nM |
| 体外活性 | 在乳腺癌小鼠模型中,Thiomyristoyl可抑制SIRT2及肿瘤生长,并降低c-Myc蛋白水平.Thiomyristoyl的抗癌效应与c-Myc水平降低成正相关. |
| 体内活性 | Thiomyristoyl对SIRT3/5/6/7抑制效果很弱。Thiomyristoyl可降低体外癌症细胞中c-MYC的水平,在不同细胞系中其对c-MYC水平的降低程度与细胞系本身对Thiomyristoyl的敏感性成正比。 |
| 细胞实验 | Human MCF-7 cells are grown in DMEM media contained 10% (vol/vol) heat-inactivated fetal bovine serum and 1% penicillin-streptomycin and treated with in the presence of 200 nM TSA for 6 hr. The acetylation level of p53 protein is determined by western blot using anti-acetyl-p53 (K382) antibody. β-actin serves as a loading control. (Only for Reference) |
| 分子量 | 581.85 |
| 分子式 | C34H51N3O3S |
| CAS No. | 1429749-41-6 |
| Smiles | CCCCCCCCCCCCCC(=S)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccccc1 |
| 密度 | 1.077 g/cm3 (Predicted) |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 100 mg/mL (171.87 mM), Sonication is recommended. Chloroform: Soluble H2O: < 1 mg/mL (insoluble or slightly soluble) | |||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (6.87 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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