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5-Iodotubercidin (NSC-113939) 是一种 ATP 类似物,有效抑制腺苷激酶,IC50为 26 nM。它可以激活磷酸化酶和糖原合成酶,在离体肝细胞中启动糖原合成。它也抑制 CK1、胰岛素受体酪氨酸激酶、磷酸化酶激酶、PKA、CK2、PKC 和 Haspin 。


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5-Iodotubercidin (NSC-113939) 是一种 ATP 类似物,有效抑制腺苷激酶,IC50为 26 nM。它可以激活磷酸化酶和糖原合成酶,在离体肝细胞中启动糖原合成。它也抑制 CK1、胰岛素受体酪氨酸激酶、磷酸化酶激酶、PKA、CK2、PKC 和 Haspin 。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 283 | In stock | |
| 5 mg | ¥ 645 | In stock | |
| 10 mg | ¥ 1,090 | In stock | |
| 25 mg | ¥ 2,510 | In stock | |
| 50 mg | ¥ 3,730 | In stock | |
| 100 mg | ¥ 5,330 | In stock | |
| 200 mg | ¥ 7,400 | 待询 | |
| 1 mL x 10 mM (in DMSO) | ¥ 593 | In stock | 
5-Iodotubercidin 相关产品
| 产品描述 | 5-Iodotubercidin (NSC-113939) is a potent adenosine kinase inhibitor with IC50 of 26 nM. It inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC. | 
| 靶点活性 |  Adenosine kinase:NA | 
| 体外活性 | 5-Iodotubercidin(Itu)是一种具有抗肿瘤活性的基因毒性药物,能够激活Atm-p53途径。与其他核苷类似物相比,Itu独特之处在于它以p53依赖的方式诱导G2阶段阻滞。此外,在较高剂量下,Itu可能激活p53独立途径,这可能与p53合作,杀死细胞并抑制肿瘤生长。Itu代谢产物整合到DNA中会导致DNA断裂,从而触发DNA损伤响应。Itu可能是一种具有独特作用机制的潜在化疗化合物[2]。 | 
| 体内活性 | 5-Iodotubercidin是一种在大鼠大脑中强效的腺苷激酶抑制剂。该化合物在小鼠中表现出显著的降血压、肌肉松弛及降低体温作用,这些效果可被茶碱(一种腺苷受体拮抗剂)阻断。尽管已知5-Iodotubercidin (1 mg/kg, i.p.)在缺血发作前使用可以增强脑片段中的细胞外腺苷水平,但其在通过运动或组织病理学指标评估时,未能提供任何脑保护作用。 | 
| 激酶实验 | AK activity is measured in a radiochemical assay. The final reaction volume is 100 μL and contained 70 mM Tris-maleate (pH 7.0), 0.1% (w/v) bovine serum albumin, 1.0 mM MgCl2, 1.0 mM ATP, 1.0 μM [U-14C]adenosine (400-600 mCi/mmol) and various inhibitor concentrations. Inhibitors are prepared as 10 mM stock solutions in DMSO. The final DMSO concentration in the assay is 5% (v/v). Eleven different concentration of the test solutions ranging from 0.001 to 10.0 μM are utilized to determine a dose response curve of the inhibition of the enzyme. Reactions are started by adding the appropriate amount of purified human recombinant AK and incubated for 20 min at 37°C. The reactions are terminated by addition of the potent AKI GP3269. A 30-μL aliquot of each reaction is spotted on DEAE cellulose filter paper (cut in squares of appr 1×1 cm) and air-dried for 30 min. The dry filters are then washed for 3 min in deionized water to remove residual [U-14C]adenosine, rinsed with ethanol and dried at 90°C for 20 min. The filter papers are counted in 5.5 mL of Ready Safe liquid scintillation cocktail using a Beckman LS3801 scintillation counter. Control AK activity is determined from the amount of [14C]AMP formed in the presence of 5% DMSO. The concentration of inhibitor required to inhibit 50% of the AK activity (IC50) is determined graphically from plots of inhibitor concentration versus percent (%) control enzyme activity. | 
| 细胞实验 | HeLa cells are grown in DME supplemented with 10% fetal bovine serum (FBS) and 2 mM?l-glutamine. Nocodazole is used at a concentration of 3.3 μM unless differently specified. Thymidine (2.5 mM) is used in the asssay. For transfection, FuGENE 6 Transfection Agent is used at a 3:1 ratio with plasmid DNA. Cells are analyzed 24-48 h after transfection. | 
| 动物实验 | Animal Models: Male Mongolian gerbilsFormulation: salineDosages: 1, 2.5 and 5 mg/kgAdministration: i.p. | 
| 别名 | NSC 113939, 5-碘代杀结核菌素, 5-ITu | 
| 分子量 | 392.15 | 
| 分子式 | C11H13IN4O4 | 
| CAS No. | 24386-93-4 | 
| Smiles | Nc1ncnc2n(cc(I)c12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 
| 密度 | 2.49 g/cm3 (Predicted) | 
| 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: 19.6 mg/mL (49.98 mM), Sonication is recommended.  | |||||||||||||||||||||||||
| 溶液配制表 | ||||||||||||||||||||||||||
| DMSO 
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 比如您的给药剂量是 10 mg/kg ,每只动物体重 20 g ,给药体积 100 μL ,
比如您的给药剂量是 10 mg/kg ,每只动物体重 20 g ,给药体积 100 μL ,  一共给药动物 10 只 ,您使用的配方为 5%
 一共给药动物 10 只 ,您使用的配方为 5%  DMSO+ 30%PEG300+ 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为 2 mg/mL 。
DMSO+ 30%PEG300+ 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为 2 mg/mL 。 
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