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Guanosine 5'-diphosphate

Synonyms: 鸟苷-5ˊ-二磷酸, GDP
货号 T7210Cas号 146-91-8 一键复制产品信息纯度: 99.89%
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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

一键复制产品信息
Rating icon 很棒

纯度: 99.89%

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
其他形式的 “Guanosine 5'-diphosphate”:
规格价格库存数量
5 mg
¥ 348
现货
10 mg
¥ 497
现货
25 mg
¥ 732
现货
50 mg
¥ 867
现货
100 mg
¥ 1,590
现货
200 mg
¥ 2,390
现货
500 mg
¥ 3,970
现货
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选择批次:
纯度: 99.89%
颜色: 白色
资源下载: COA HNMR LCMS产品操作手册

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)
储存&溶解度
存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

实际储存温度请以COA为准

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
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

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:
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 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 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:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 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: DMSOPEG300PEG400Tween 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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