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Adenosine-5'-diphosphate

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产品名称: Adenosine-5'-diphosphate
产品型号: GOY-Y0520
产品展商: 谷研
产品文档: 无相关文档
发布时间:2023-04-11

简单介绍

Adenosine-5'-diphosphate≥ 21.35mg/mL in DMSO with gentle warming


Adenosine-5'-diphosphate  的详细介绍

性能参数

产品名称

Adenosine-5'-diphosphate

规格

100mg 250mg 500mg 1g

货号

GOY-Y0520

 含量

>98.00%

CAS

58-64-0

别名

Adenosine Pyrophosphate,ADP,5′-ADP

 

 

化学名

adenosine 5'-(trihydrogen diphosphate)

分子式

C10H15N5O10P2

分子量

分子 427.2

溶解度

≥ 21.35mg/mL in DMSO with gentle warming

储存条件

Store at -20°C

General tips

 

用途

仅供科研

价格

电询

详细内容

IC50: 67 nM for P2X2/3

Adenosine-5'-diphosphate is an agonist of purinergic receptors.

Purinergic receptors, also known as purinoceptors, are a family of plasma membrane molecules that are found in almost all mammalian tissues. Within the field of purinergic signalling, these receptors have been implicated in learning and memory, locomotor and feeding behavior, and sleep. More specifically, purinergic receptors are involved in several cellular functions, such as proliferation and migration of neural stem cells, vascular reactivity, apoptosis and cytokine secretion.

In vitro: Adenosine 5'-diphosphate (ADP) is an adenine nucleotide having two phosphate groups esterified to the sugar moiety at the 5’ position. ADP is formed through dephosphorylation of adenosine 5’-triphosphate (ATP) by ATPases and can be converted back to ATP by ATP synthases. ADP can also be metabolized to adenosine 5’-monophosphate (AMP) and 2’-deoxyadenosine 5’-diphosphate (dADP). ADP can modulate several receptors, such as activating certain purinergic receptors and inhibiting others, inhibiting rat ecto-5’nucleotidase (Ki = 0.91 nM), as well as regulating the phosphorylation status of AMP-activated protein kinase [1, 2].

In vivo: Up to now, there is no animal in vivo data reported.

Clinical trial: So far, no clinical study has been conducted.

References:

1.  Azran, S.,Frster, D.,Danino, O., et al. Highly efficient biocompatible neuroprotectants with dual activity as antioxidants and P2Y receptor agonists. J. Med. Chem. 56(12), 4938-4952 (2013).

2.  Jarvis, M.F.,Bianchi, B.,Uchic, J.T., et al. [3H]A-317491, a novel high-affinity non-nucleotide antagonist that specifically labels human P2X2/3 and P2X3 receptors. Journal of Pharmacology and Experimental Therapeutics 310(1), 407-416 (2004).

 

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