A4386
腺苷-5′-二磷酸 双环己铵盐
≥95% (HPLC), crystalline, bacterial
别名:
A2P5P, ADP
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关于此项目
经验公式（希尔记法）:
C10H15N5O10P2 · 2C6H13N
化学文摘社编号:
分子量:
625.55
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
产品名称
腺苷-5′-二磷酸 双环己铵盐, ≥95% (HPLC), crystalline, bacterial
InChI
1S/C10H15N5O10P2.2C6H13N/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20;2*7-6-4-2-1-3-5-6/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20);2*6H,1-5,7H2/t4-,6-,7-,10-;;/m1../s1
SMILES string
NC1CCCCC1.NC2CCCCC2.Nc3ncnc4n(cnc34)[C@@H]5O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]5O
InChI key
SCOUEIPNDLFPCX-IDIVVRGQSA-N
biological source
bacterial
assay
≥95% (HPLC)
form
crystalline
solubility
H2O: soluble, clear to slightly hazy, colorless to faintly yellow
storage temp.
−20°C
Quality Level
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相关类别
Application
5′-二磷酸腺苷（ADP）是通过ATP合酶转化为ATP而参与能量储存和核酸代谢的腺嘌呤核苷酸。ADP通过其与ADP受体P2Y1、P2Y12和P2X1的相互作用影响血小板活化。 在通过ecto-ADP酶转化为腺苷后，通过腺苷受体抑制血小板活化。
腺苷-5′-二磷酸二环己胺盐已被用作发光测定（luminometry）中的标准品。它也已用于苏拉明抑制分析。
Disclaimer
稳定，不吸潮
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
The trypanocidal drug suramin and other trypan blue mimetics are inhibitors of pyruvate kinases and bind to the adenosine site
Morgan HP, et al.
The Journal of Biological Chemistry, 286(36), 31232-31240 (2011)
Effects of anticoagulants used during blood collection on human platelet function
May J A and Heptinstall S
Platelets and megakaryocytes, 3-11 (2004)
Béatrice Hechler et al.
Purinergic signalling, 7(3), 293-303 (2011-07-28)
Following vessel wall injury, platelets adhere to the exposed subendothelium, become activated and release mediators such as TXA(2) and nucleotides stored at very high concentration in the so-called dense granules. Released nucleotides and other soluble agents act in a positive
David Erlinge
Advances in pharmacology (San Diego, Calif.), 61, 417-439 (2011-05-19)
The purine- and pyrimidine-sensitive P2Y receptors belong to the large group of G-protein-coupled receptors that are the target of approximately one-third of the pharmaceutical drugs used in the clinic today. It is therefore not unexpected that the P2Y receptors could
Sarah Jones et al.
British journal of haematology, 153(1), 83-91 (2011-02-22)
ADP is considered a weak platelet agonist due to the limited aggregation responses it induces in vitro at physiological concentrations of extracellular Ca(2+) [(Ca(2+) )(o) ]. Lowering [Ca(2+) ](o) paradoxically enhances ADP-evoked aggregation, an effect that has been attributed to
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