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Guanosine 5'-diphosphate

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纯度: 99.52%

货号 T7210Cas号 146-91-8

别名 鸟苷-5ˊ-二磷酸, GDP

Guanosine 5'-diphosphate (GDP) 是核苷二磷酸,是潜在的铁动员剂,能够阻断铁调素-铁转运蛋白相互作用并调节白细胞介素-6 (IL-6)/stat-3 途径。

Guanosine 5'-diphosphate

Guanosine 5'-diphosphate

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Rating icon 还可以

纯度: 99.52%

货号 T7210 别名 鸟苷-5ˊ-二磷酸, GDPCas号 146-91-8

Guanosine 5'-diphosphate (GDP) 是核苷二磷酸,是潜在的铁动员剂,能够阻断铁调素-铁转运蛋白相互作用并调节白细胞介素-6 (IL-6)/stat-3 途径。

规格价格库存数量
5 mg
¥ 348
5日内发货
10 mg
¥ 497
5日内发货
25 mg
¥ 732
5日内发货
50 mg
¥ 867
5日内发货
100 mg
¥ 1,590
5日内发货
200 mg
¥ 2,390
5日内发货
500 mg
¥ 3,970
5日内发货
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产品介绍


Guanosine 5'-diphosphate AI Summary
Guanosine 5'-diphosphate demonstrates a broad spectrum of bioactivities across multiple targets and assays. It inhibits fucosyltransferase enzymes, including Fucosyltransferase 4 alpha 1,3 with an IC50 value of 5000.0 nM, Fucosyltransferase (FucT V) with an IC50 value of 67000.0 nM, and human recombinant alpha1,3-fucosyltransferase 9 with a Ki of 77900.0 nM and an IC50 of 59000.0 nM. Moreover, it inhibits Helicobacter pylori recombinant alpha1,3-fucosyltransferase with an inhibition percentage of up to 75.0%. In addition, it has a binding affinity to Escherichia coli KPR (Kd of 373000.0 nM) and shows an inhibition of 8.5% on Trypanosoma brucei brucei DPMS at 1 mM. In terms of receptor activity, Guanosine 5'-diphosphate acts as an agonist at human recombinant P2Y2, P2Y4, and P2Y6 receptors, with respective EC50 values of 54.0, 90.0, and 45000.0 nM, mediated by PLC and [3H]IP production. It also induces phagocytosis in Wistar rat microglia, showing 49.7% activity at 100 uM over 20 minutes. Furthermore, the compound exhibits bioactivity in several other assays: it enhances SMN2 splice variant expression (potency of 14125.4 nM), inhibits Aldehyde Dehydrogenase 1 (ALDH1A1) with a potency of 2818.4 nM, and inhibits Regulator of G Protein Signaling (RGS) 4 with a potency of 597.3 nM. It also shows binding affinity to Mg2+ ions as determined by 31P NMR analysis with activities of 0.5 and 2.0 equiv, and interacts with various mutants of Rab7 GTPase and wild-type Rab7 with Kd values ranging from 25.83 nM to 109.2 nM, suggesting potential modulatory effects on Rab7 GTPase functions..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Guanosine 5'-diphosphate (GDP) as Potential Iron Mobilizer, Preventing the Hepcidin-Ferroportin Interaction and Modulating the Interleukin-6/Stat-3 Pathway.
别名鸟苷-5ˊ-二磷酸, GDP
化学信息
分子量443.2
分子式C10H15N5O11P2
CAS No.146-91-8
SmilesO[C@H]1[C@H](N2C3=C(N=C2)C(=O)N=C(N)N3)O[C@H](COP(OP(=O)(O)O)(=O)O)[C@H]1O
密度2.63 g/cm3 (Predicted)
颜色White
物理性状solid
储存&溶解度
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
H2O: 50 mg/mL (112.82 mM), Sonication is recommended.
溶液配制表
H2O
1mg5mg10mg50mg
1 mM2.2563 mL11.2816 mL22.5632 mL112.8159 mL
5 mM0.4513 mL2.2563 mL4.5126 mL22.5632 mL
10 mM0.2256 mL1.1282 mL2.2563 mL11.2816 mL
20 mM0.1128 mL0.5641 mL1.1282 mL5.6408 mL
50 mM0.0451 mL0.2256 mL0.4513 mL2.2563 mL
100 mM0.0226 mL0.1128 mL0.2256 mL1.1282 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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