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首页 / 抑制剂/激动剂 / G蛋白偶联受体/G蛋白 / P2Y受体 / Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 {[allProObj[0].p_purity_real_show]}

货号:A203590 同义名: UDP-D-Glucose disodium salt; UDPG

Uridine 5′-diphosphoglucose disodium salt是一种葡萄糖含量寡糖、多糖、糖蛋白和糖脂的前体,并且是 P2Y14 受体的激动剂。

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 化学结构 CAS号:28053-08-9
Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 化学结构
CAS号:28053-08-9
Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 3D分子结构
CAS号:28053-08-9
Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 化学结构 CAS号:28053-08-9
Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 3D分子结构 CAS号:28053-08-9
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Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 纯度/质量文件 产品仅供科研

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Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 细胞实验

Cell Line
Concentration Treated Time Description References
RBL-2H3 mast cells 10 µM 1-60 minutes To investigate the effect of UDPG on MAPK activation. Results showed that UDPG induced phosphorylation of ERK1/2, P38, and JNK, and ERK1/2 activation was PTX-sensitive. Biochem Pharmacol. 2010 Mar 15;79(6):873-9
COS-7 cells 0.35 ± 0.12 µM 20 minutes To evaluate the agonist activity of UDPG at the P2Y14 receptor, showing an EC50 of 0.35 ± 0.12 µM. J Med Chem. 2007 May 3;50(9):2030-9
RBL-2H3 mast cells 1150 ± 320 nM (EC50) 20 minutes To investigate the role of UDPG in mediating mast cell degranulation via P2Y14 receptor. Results showed that UDPG and its analog MRS2690 enhanced antigen-induced HEX release in a concentration-dependent manner, and this effect was blocked by pertussis toxin and P2Y14 receptor-specific siRNA. Biochem Pharmacol. 2010 Mar 15;79(6):873-9
Rat cortical neurons 100 µM 24 hours To evaluate the effect of UDP-G on neuronal apoptosis, results showed UDP-G decreased cell viability, increased apoptotic marker CC3 levels and TUNEL positive neurons Stroke. 2024 May;55(5):1381-1392
INS-1 832/13 cells 10 µM 24 hours To investigate the effect of UDP-G on cell proliferation, results showed that UDP-G suppressed cell proliferation under high glucose conditions. J Biol Chem. 2020 Nov 6;295(45):15245-15252
INS-1 832/13 cells 10 µM 60 minutes To investigate the effect of UDP-G on GSIS, results showed that UDP-G suppressed GSIS and was associated with suppression of cAMP. J Biol Chem. 2020 Nov 6;295(45):15245-15252
Human pancreatic islets 10 µM 60 minutes To investigate the effect of UDP-G on glucose-stimulated insulin secretion (GSIS), results showed that UDP-G dose-dependently suppressed GSIS. J Biol Chem. 2020 Nov 6;295(45):15245-15252
INS-1 832/13 cells 10 µM 72 hours To investigate the effect of UDP-G on apoptosis, results showed that UDP-G increased apoptosis under high glucose conditions. J Biol Chem. 2020 Nov 6;295(45):15245-15252
Human pancreatic islets 10 µM 72 hours To investigate the effect of UDP-G on islet cell reductive capacity, results showed that UDP-G decreased the reductive capacity of islets. J Biol Chem. 2020 Nov 6;295(45):15245-15252

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Sprague-Dawley rats Subarachnoid hemorrhage model Intranasal administration 7.1 mg/kg Administered at 1h after SAH, short-term study at 24h, long-term study at 28 days To evaluate the role of UDP-G/P2Y14 signaling in SAH, results showed PPTN improved neurological function and reduced neuronal apoptosis, while UDP-G exacerbated these outcomes Stroke. 2024 May;55(5):1381-1392

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 参考文献

[1]DietrichKeppler, et al. Uridine-5′-diphosphoglucose. Methods of Enzymatic Analysis (Second English Edition). 1974;4:2225-2228.

[2]Das A, et al. Human P2Y(14) receptor agonists: truncation of the hexose moiety of uridine-5'-diphosphoglucose and its replacement with alkyl and aryl groups. J Med Chem. 2010 Jan 14;53(1):471-80.

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.64mL

0.33mL

0.16mL

8.19mL

1.64mL

0.82mL

16.39mL

3.28mL

1.64mL

Uridine 5′-diphosphoglucose disodium salt/二磷酸尿苷葡萄糖二钠盐 技术信息

CAS号28053-08-9
分子式C15H22N2Na2O17P2
分子量 610.27
SMILES Code O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)OP([O-])(OP([O-])(OC[C@H]2O[C@H]([C@@H]([C@@H]2O)O)N3C=CC(NC3=O)=O)=O)=O.[Na+].[Na+]
MDL No. MFCD00077895
别名 UDP-D-Glucose disodium salt; UDPG; UYD77NZ2JQ; Uridine 5'-diphosphoglucose disodium; Disodium UDP-glucose; 28053-08-9; Uridine(5')disodiodiphospho(1)-alpha-D-glucose; UDP-α-D-Glucose sodium salt; UDP-Glc; Uridine 5'-diphosphoglucose disodium salt
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 110 mg/mL(180.25 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 250 mg/mL(409.66 mM)

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
方案 二
配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
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