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Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?)

Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?) structure

Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?) 

structure
  • CAS No:

    20398-34-9

  • Formula:

    C10H15N5O10P2.xNa

  • Chemical Name:

    Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?)

  • Synonyms:

    Adenosine 5′-(trihydrogen diphosphate),sodium salt (1:?);Adenosine 5′-(trihydrogen pyrophosphate),sodium salt;Adenosine 5′-(trihydrogen diphosphate),sodium salt;Sodium adenosine diphosphate;ADP sodium salt;Adenosine 5′-diphosphate sodium salt;Sodium adenosine 5′-diphosphate

  • Categories:

    Biochemical Engineering  >  Nucleoside Drugs

Description

Adenosine 5'-diphosphate (ADP) sodium salt is a nucleoside diphosphate, which is the product of ATP dephosphorylation by ATPases. Adenosine 5'-diphosphate sodium salt induces human platelet aggregation and inhibits stimulated adenylate cyclase by an action at P2T-purinoceptors[1][2][3].

Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?) Basic Attributes

493.15

492.975250

218-249-0

29349990

Characteristics

241

2.49 g/cm3

877.7°C at 760 mmHg

484.6ºC

Safety Information

NONH for all modes of transport

1

R20/21/22

S36/37

Xn: Harmful;

Adenosine 5′-(trihydrogen diphosphate), sodium salt (1:?) Use and Manufacturing

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 ADP receptors P2Y1, P2Y12 and P2X1. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors.

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