B6396
2′(3′)-O-(4-苯甲酰苯甲酰)腺苷5′-三磷酸 三乙铵盐
≥93%
别名:
Bz-ATP, 苯甲酰苯甲酰-ATP
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选择尺寸
关于此项目
经验公式（希尔记法）:
C24H24N5O15P3 · xC6H15N × yH2O
化学文摘社编号:
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
生物来源
synthetic (organic)
质量水平
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
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)
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)
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
Molecular and functional properties of P2X receptors?recent progress and persisting challenges
Kaczmarek-Hajek K, et al.
Purinergic Signaling, 8(3), 375-417 (2012)
Diabetes-induced Neuropathic Mechanical Hyperalgesia Depends on P2X4 Receptor Activation in Dorsal Root Ganglia
Teixeira JM, et al.
Neuroscience, 398, 158-170 (2019)
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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