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Merck

01897

Sigma-Aldrich

Adenosin-5′-diphosphat Dinatriumsalz

≥90%

Synonym(e):

5′-ADP-Na2

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About This Item

Empirische Formel (Hill-System):
C10H13N5Na2O10P2
CAS-Nummer:
Molekulargewicht:
471.16
Beilstein:
7563620
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41106305
eCl@ss:
32160414
PubChem Substanz-ID:
NACRES:
NA.51

Assay

≥90%

Form

powder or crystals

Optische Aktivität

[α]20/D −29.6±1°, c = 0.5% in 0.5 M Na2HPO4

Verunreinigungen

≤10% water

Lagertemp.

−20°C

SMILES String

[Na+].[Na+].Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP([O-])(=O)OP(O)([O-])=O)[C@@H](O)[C@H]3O

InChI

1S/C10H15N5O10P2.2Na/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;;/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20);;/q;2*+1/p-2/t4-,6-,7-,10-;;/m1../s1

InChIKey

ORKSTPSQHZNDSC-IDIVVRGQSA-L

Verwandte Kategorien

Anwendung

Adenosine 5′-diphosphate disodium salt has been used as a purinergic G protein-coupled receptor P2Y12 agonistin platelet activation tests in blood samples.

Biochem./physiol. Wirkung

Adenosine 5′-diphosphate (ADP) is an adenine nucleotide involved in energy storage and nucleic acid metabolism via its conversion into ATP by ATP synthases. ADP affects platelet activation through its interaction with purinergic receptors P2Y1 and P2Y12. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Cécile H Kicken et al.
PloS one, 12(2), e0172265-e0172265 (2017-02-17)
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Dana Huskens et al.
PloS one, 13(2), e0192079-e0192079 (2018-02-02)
Platelet function testing with flow cytometry has additional value to existing platelet function testing for diagnosing bleeding disorders, monitoring anti-platelet therapy, transfusion medicine and prediction of thrombosis. The major challenge is to use this technique as a diagnostic test. The
Lihui Long et al.
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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

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