所有图片(3)
About This Item
经验公式(希尔记法):
C24H24N5O15P3 · xC6H15N × yH2O
CAS号:
分子量:
715.39 (anhydrous free acid basis)
MDL编号:
UNSPSC代码:
12352202
PubChem化学物质编号:
NACRES:
NA.77
推荐产品
生物来源
synthetic (organic)
方案
≥93%
表单
powder
溶解性
water: 50 mg/mL, clear, colorless to faintly yellow
储存温度
−20°C
SMILES字符串
CCN(CC)CC.Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](OC(=O)c4ccc(cc4)C(=O)c5ccccc5)[C@H]3O
InChI
1S/C24H24N5O15P3.C6H15N/c25-21-17-22(27-11-26-21)29(12-28-17)23-19(31)20(16(41-23)10-40-46(36,37)44-47(38,39)43-45(33,34)35)42-24(32)15-8-6-14(7-9-15)18(30)13-4-2-1-3-5-13;1-4-7(5-2)6-3/h1-9,11-12,16,19-20,23,31H,10H2,(H,36,37)(H,38,39)(H2,25,26,27)(H2,33,34,35);4-6H2,1-3H3/t16-,19-,20-,23-;/m1./s1
InChI key
HVOVBTNCGADRTH-WBLDMZOZSA-N
相关类别
一般描述
2′(3′)-O-(4-苄基苯甲酰基)腺苷5′-三磷酸酯是ATP的光反应类似物。
应用
2′(3′)-O-(4-苯甲酰基苯甲酰基)腺苷5′-三磷酸三乙铵盐已被用作大鼠肾脏切片、I型糖尿病诱发大鼠和星形胶质细胞−神经元共培养物中的P2X4受体激动剂。它还被用作等渗E3培养基中的合成ATP类似物。
可用作蛋白质和酶光亲和标记结合ATP。
生化/生理作用
2′(3′)-O-(4-苄基苯甲酰基)腺苷5′-三磷酸三乙铵盐是一种选择性嘌呤能受体(P2X)激动剂。在同源二聚体P2X7受体上,它比ATP更有效。它还可有效激活P2X1、P2X2和P2X3受体。可用作蛋白质和酶光亲和标记结合ATP。
选择性P2X嘌呤能激动剂。 在同源二聚体P2X7受体上,它比ATP更有效。
其他说明
混合异构体
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
其他客户在看
Juan Francisco Codocedo et al.
PloS one, 8(3), e57626-e57626 (2013-03-09)
To assess the putative role of adenosine triphosphate (ATP) upon nitric oxide (NO) production in the hippocampus, we used as a model both rat hippocampal slices and isolated hippocampal neurons in culture, lacking glial cells. In hippocampal slices, additions of
Covalent binding of 3'-O-(4-benzoyl) benzoyl adenosine 5'-triphosphate (BzATP) to the isolated alpha and beta subunits and the alpha 3 beta 3 core complex of TF1. Covalent binding of BzATP prevents association of alpha and beta subunits and induces dissociation of the alpha 3 beta 3 core complex.
BarZvi D, et al.
The Journal of Biological Chemistry, 267(16), 11029-11033 (1992)
Diabetes-induced Neuropathic Mechanical Hyperalgesia Depends on P2X4 Receptor Activation in Dorsal Root Ganglia
Teixeira JM, et al.
Neuroscience, 398, 158-170 (2019)
Molecular and functional properties of P2X receptors?recent progress and persisting challenges
Kaczmarek-Hajek K, et al.
Purinergic Signaling, 8(3), 375-417 (2012)
Ji Zhao et al.
Molecular neurodegeneration, 4, 4-4 (2009-01-16)
Insulin-degrading enzyme (IDE) is a ubiquitously expressed zinc-metalloprotease that degrades several pathophysiologically significant extracellular substrates, including insulin and the amyloid beta-protein (Abeta), and accumulating evidence suggests that IDE dysfunction may be operative in both type 2 diabetes mellitus and Alzheimer
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