Guanosine-5'-triphosphate disodium salt
(Synonyms: 鸟苷-5'-三磷酸二钠盐,5'-GTP disodium salt) 目录号 : GC61932
Guanosine-5'-triphosphate disodium salt是一种在生物合成和细胞信号转导中发挥关键作用的核苷酸。
Cas No.:56001-37-7
Sample solution is provided at 25 µL, 10mM.
Guanosine-5'-triphosphate disodium salt is a nucleotide that plays a critical role in biosynthesis and cellular signal transduction[1]. Guanosine-5'-triphosphate disodium salt serves as a phosphate group donor, participates in protein synthesis processes, and activates G protein-mediated signaling pathways[2]. Guanosine-5'-triphosphate disodium salt acts as a high-energy mononucleotide precursor in the enzymatic biosynthesis of DNA and RNA. Guanosine-5'-triphosphate disodium salt can promoting the differentiation of myogenic cells and showing potential for applications in studies such as skeletal muscle regeneration[3-4].
In vitro, treatment of PC12 cells with Guanosine-5'-triphosphate disodium salt (300μM) for 48 hours promotes neurite outgrowth[5]. Treatment of C2C12 mouse myoblasts with Guanosine-5'-triphosphate disodium salt (500μM) for 48 hours induces a transient increase in intracellular calcium concentration, activates intermediate-conductance calcium-activated potassium channels (IKCa), and leads to membrane hyperpolarization[6]. Exposure of human myogenic precursor cells to Guanosine-5'-triphosphate disodium salt (500μM) for 24 hours significantly upregulates the expression of the myogenic regulator Myogenin and specifically enhances the expression of miR-133a and miR-133b[7]. Treatment of PC12 cells with Guanosine-5'-triphosphate disodium salt (300μM) for 48 hours induces a sustained increase in intracellular calcium concentration by activating specific GTP-binding sites on the cell surface (Kd=52.9μM), an effect dependent on the activation of L-type voltage-gated calcium channels[8].
References:
[1] Pendergrass JC, Haley BE. Inhibition of brain tubulin-guanosine 5'-triphosphate interactions by mercury: similarity to observations in Alzheimer's diseased brain. Met Ions Biol Syst. 1997;34:461-78.
[2] Kaziro Y. The role of guanosine 5'-triphosphate in polypeptide chain elongation. Biochim Biophys Acta. 1978 Sep 21;505(1):95-127.
[3] Lin D, Cui F, Bu Q, et al. The expression and clinical significance of GTP-binding RAS-like 3 (ARHI) and microRNA 221 and 222 in prostate cancer. J Int Med Res. 2011;39(5):1870-5.
[4] Pietrangelo T, Guarnieri S, Fulle S, et al. Signal transduction events induced by extracellular guanosine 5' triphosphate in excitable cells. Purinergic Signal. 2006 Nov;2(4):633-6.
[5] Gysbers JW, Rathbone MP. GTP and guanosine synergistically enhance NGF-induced neurite outgrowth from PC12 cells. Int J Dev Neurosci. 1996 Feb;14(1):19-34.
[6] Pietrangelo T, Fioretti B, Mancinelli R, et al. Extracellular guanosine-5'-triphosphate modulates myogenesis via intermediate Ca(2+)-activated K+ currents in C2C12 mouse cells. J Physiol. 2006 May 1;572(Pt 3):721-33.
[7] Pietrangelo T, Di Filippo ES, Locatelli M, et al. Extracellular Guanosine 5'-Triphosphate Induces Human Muscle Satellite Cells to Release Exosomes Stuffed With Guanosine. Front Pharmacol. 2018 Mar 16;9:152.
[8] Gysbers JW, Guarnieri S, Mariggiò MA, et al. Extracellular guanosine 5' triphosphate enhances nerve growth factor-induced neurite outgrowth via increases in intracellular calcium. Neuroscience. 2000;96(4):817-24.
Guanosine-5'-triphosphate disodium salt是一种在生物合成和细胞信号转导中发挥关键作用的核苷酸[1]。Guanosine-5'-triphosphate disodium salt能够作为磷酸基团的供体,参与蛋白质的合成过程并激活G蛋白介导的信号通路[2]。Guanosine-5'-triphosphate disodium salt还是DNA和RNA酶促生物合成中高能量的单核苷酸单元前体,并可上调特定microRNA的表达,从而促进肌源性细胞的分化,在骨骼肌再生等研究中具有应用潜力[3-4]。
在体外,Guanosine-5'-triphosphate disodium salt(300μM)处理PC12细胞48小时,可促进神经突生长[5]。Guanosine-5'-triphosphate disodium salt(500μM)处理C2C12小鼠成肌细胞48小时,可诱导细胞内钙离子浓度瞬时升高,激活中间电导钙激活钾通道(IKCa),引起细胞膜超极化[6]。Guanosine-5'-triphosphate disodium salt(500μM)处理人肌源性前体细胞24小时,可显著上调成肌调节因子Myogenin基因表达,并特异性促进miR-133a和miR-133b的表达[7]。Guanosine-5'-triphosphate disodium salt(300μM)处理PC12细胞48小时,可通过激活细胞表面特异性GTP结合位点(Kd= 52.9μM)诱导细胞内钙离子浓度持续升高,该效应依赖于L型电压门控钙通道的激活[8]。
| Cell experiment [1]: | |
Cell lines | PC12 cells (rat pheochromocytoma cell line) |
Preparation Method | PC12 cells were maintained in RPMI-1640 medium supplemented with 5% fetal calf serum and 5% heat-inactivated horse serum. For neurite outgrowth assays, cells were plated on poly-DL-ornithine-coated plates in medium containing 1.5% serum and treated with Guanosine-5'-triphosphate disodium salt (300µM) in the presence or absence of 40ng/ml Nerve Growth Factor (NGF). |
Reaction Conditions | 300µM; 48h. |
Applications | Extracellular Guanosine-5'-triphosphate disodium salt synergistically enhanced NGF-induced neurite outgrowth, increasing the proportion of cells with neurites from 20-35% (NGF alone) to 40-65%. This effect was mediated by a sustained increase in intracellular Ca²⁺ concentration ([Ca²⁺]i) via influx through L-type voltage-gated calcium channels and Ca²⁺-induced Ca²⁺ release (CICR) from intracellular ryanodine-sensitive stores. |
References: | |
| Cas No. | 56001-37-7 | SDF | |
| 别名 | 鸟苷-5'-三磷酸二钠盐,5'-GTP disodium salt | ||
| Canonical SMILES | O[C@@H]([C@H]([C@H](N1C=NC2=C1N=C(N)NC2=O)O3)O)[C@H]3COP([O-])(OP(O)(OP([O-])(O)=O)=O)=O.[Na+].[Na+] | ||
| 分子式 | C10H14N5Na2O14P3 | 分子量 | 567.14 |
| 溶解度 | Water : 125 mg/mL (220.40 mM) | 储存条件 | 4°C, protect from light |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
||
| Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
![]() |
1 mg | 5 mg | 10 mg |
| 1 mM | 1.7632 mL | 8.8162 mL | 17.6323 mL |
| 5 mM | 352.6 μL | 1.7632 mL | 3.5265 mL |
| 10 mM | 176.3 μL | 881.6 μL | 1.7632 mL |
| 第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
| 给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
| 第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
















