Adenosine 5′-diphosphoribose sodium
(Synonyms: 二磷酸腺苷核糖; ADP ribose sodium) 目录号 : GC19729
Adenosine 5′-diphosphoribose sodium是一种核苷酸衍生物,是Transient receptor potential melastatin 2 (TRPM2)激动剂,在细胞内多种代谢途径中发挥着重要作用。
Cas No.:68414-18-6
Sample solution is provided at 25 µL, 10mM.
Adenosine 5′-diphosphoribose sodium is a nucleotide derivative and an agonist of Transient receptor potential melastatin 2 (TRPM2), playing an important role in various metabolic pathways within cells[1]. Adenosine 5′-diphosphoribose sodium can modulate intracellular signaling pathways, affecting processes such as cell proliferation, differentiation, and apoptosis[2]. Adenosine 5′-diphosphoribose sodium also plays a key role in cellular stress responses, helping cells cope with adverse conditions like oxidative stress[3]. Adenosine 5′-diphosphoribose sodium is closely related to cellular immune responses, participating in the regulation of immune cell activity[4].
In vitro, treatment of RIN-5F cells with Adenosine 5′-diphosphoribose sodium (100μM) increases intracellular calcium ion (Ca²⁺) concentration through the PLC-IP3 pathway[5]. Treatment of microglial cells with Adenosine 5′-diphosphoribose sodium (1mM) induces Ca²⁺ and Mg²⁺ influx[6].
References:
[1] Fliegert R, Bauche A, Wolf Pérez AM, et al. 2'-Deoxyadenosine 5'-diphosphoribose is an endogenous TRPM2 superagonist. Nat Chem Biol. 2017 Sep;13(9):1036-1044.
[2] Vyas S, Chang P. New PARP targets for cancer therapy. Nat Rev Cancer. 2014 Jul;14(7):502-9.
[3] Dousa TP, Chini EN, Beers KW. Adenine nucleotide diphosphates: emerging second messengers acting via intracellular Ca2+ release. Am J Physiol. 1996 Oct;271(4 Pt 1):C1007-24.
[4] Ji D, Luo ZW, Ovcjak A, et al. Role of TRPM2 in brain tumours and potential as a drug target. Acta Pharmacol Sin. 2022 Apr;43(4):759-770.
[5] Ishii M, Shimizu S, Hagiwara T, et al. Extracellular-added ADP-ribose increases intracellular free Ca2+ concentration through Ca2+ release from stores, but not through TRPM2-mediated Ca2+ entry, in rat beta-cell line RIN-5F. J Pharmacol Sci. 2006 Jun;101(2):174-8.
[6] Kraft R, Grimm C, Grosse K, et al. Hydrogen peroxide and ADP-ribose induce TRPM2-mediated calcium influx and cation currents in microglia. Am J Physiol Cell Physiol. 2004 Jan;286(1):C129-37.
Adenosine 5′-diphosphoribose sodium是一种核苷酸衍生物,是Transient receptor potential melastatin 2 (TRPM2)激动剂,在细胞内多种代谢途径中发挥着重要作用[1]。Adenosine 5′-diphosphoribose sodium能够调节细胞内的信号传导通路,影响细胞的增殖、分化和凋亡等过程[2]。Adenosine 5′-diphosphoribose sodium在细胞的应激反应中也扮演着关键角色,帮助细胞应对氧化应激等不利环境[3]。Adenosine 5′-diphosphoribose sodium还与细胞的免疫反应密切相关,参与调节免疫细胞的活性[4]。
在体外,Adenosine 5′-diphosphoribose sodium(100μM)处理RIN-5F细胞,Adenosine 5′-diphosphoribose sodium通过PLC- IP3途径增加细胞内钙离子(Ca²⁺)浓度[5]。Adenosine 5′-diphosphoribose sodium(1mM)处理小胶质细胞,可诱导Ca²⁺内流和Mg²⁺内流[6]。
| Cell experiment [1]: | |
Cell lines | RIN-5F cells (rat pancreatic β-cell line) |
Preparation Method | RIN-5F cells were cultured in RPMI 1640 medium containing 10% fetal bovine serum, 100U/ml penicillin, and 100μg/ml streptomycin at 37°C. Cells were treated with extracellular-addedAdenosine 5′-diphosphoribose sodium (100μM) for 10–20 seconds. |
Reaction Conditions | 100μM; 10–20 seconds |
Applications | Extracellular Adenosine 5′-diphosphoribose sodium induced a transient increase in intracellular free Ca²⁺ concentration through Ca²⁺ release from thapsigargin-sensitive Ca²⁺ stores. |
References: | |
| Cas No. | 68414-18-6 | SDF | |
| 别名 | 二磷酸腺苷核糖; ADP ribose sodium | ||
| Canonical SMILES | O[C@H]([C@@H]1O)[C@@H](O[C@@H]1COP(OP(OC[C@@H](O)[C@@H](O)[C@@H](O)C=O)([O-])=O)(O)=O)N2C(N=CN=C3N)=C3N=C2.[Na+] | ||
| 分子式 | C₁₅H₂₂N₅NaO₁₄P₂ | 分子量 | 581.30 |
| 溶解度 | Water : 125 mg/mL (215.04 mM) | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg |
| 1 mM | 1.7203 mL | 8.6014 mL | 17.2028 mL |
| 5 mM | 344.1 μL | 1.7203 mL | 3.4406 mL |
| 10 mM | 172 μL | 860.1 μL | 1.7203 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) | ||||||||||
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| % 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,
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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。
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