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Merck

A6779

Sigma-Aldrich

高碘酸氧化腺苷 5′-三磷酸 钠盐

≥97%

别名:

oATP, 腺苷 5′-三磷酸-2′,3′-二醛

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About This Item

经验公式(希尔记法):
C10H14N5O13P3
CAS号:
分子量:
505.17
MDL號碼:
分類程式碼代碼:
41106305
eCl@ss:
32160414
PubChem物質ID:
NACRES:
NA.51

生物源

bacterial (corynebacterium sp)

化驗

≥97%

形狀

powder

儲存溫度

−20°C

SMILES 字串

[Na].Nc1ncnc2n(cnc12)[C@H](O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C=O)C=O

InChI

1S/C10H14N5O13P3.Na.H/c11-9-8-10(13-4-12-9)15(5-14-8)7(2-17)26-6(1-16)3-25-30(21,22)28-31(23,24)27-29(18,19)20;;/h1-2,4-7H,3H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20);;/t6-,7+;;/m0../s1

InChI 密鑰

IHQATUPGVKMGLT-AUCRBCQYSA-N

相关类别

一般說明

腺苷-5′-三磷酸-2′,3′-二醛是二醛的一种衍生物。

應用

腺苷-5′-三磷酸,高碘酸氧化钠盐已被用于:
  • 作为嘌呤能受体的拮抗剂(P2×7抑制P2×7通路)
  • 作为通过Ca2+评估P2x7-R活性的非特异性激动剂
  • 评估细胞内ATP水平升高的生理意义
  • 评估Flcn缺陷细胞中用于破骨细胞生成的P2rx7表达升高的生理意义

生化/生理作用

腺苷-5′-三磷酸-2′,3′-二醛被认为是P2×7受体的一种抑制剂。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Frontiers in pharmacology, 8, 638-638 (2017-09-29)
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Small (Weinheim an der Bergstrasse, Germany), 12(43), 5998-6011 (2016-09-21)
Exocytosis of single-walled carbon nanotubes (SWCNTs) determines therapeutic efficiency and toxicity of nanoproducts but its underlying mechanism remains elusive. In this study, it is found that the exocytosis mechanism of SWCNTs is mediated mainly through the activation of P2X7 receptor
Ursula Schenk et al.
Science signaling, 1(39), ra6-ra6 (2008-10-02)
T cell receptor (TCR) stimulation results in the influx of Ca(2+), which is buffered by mitochondria and promotes adenosine triphosphate (ATP) synthesis. We found that ATP released from activated T cells through pannexin-1 hemichannels activated purinergic P2X receptors (P2XRs) to
William Foulsham et al.
Scientific reports, 9(1), 8617-8617 (2019-06-15)
Adenosine triphosphate (ATP) is released into the extracellular environment during transplantation, and acts via purinergic receptors to amplify the alloimmune response. Here, using a well-established murine model of allogeneic corneal transplantation, we investigated the immunomodulatory mechanisms of the purinergic receptor

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