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4097-04-5

4097-04-5 Structure

4097-04-5 Structure
IdentificationBack Directory
[Name]

A[5']P5[5']A SODIUM SALT
[CAS]

4097-04-5
[Synonyms]

A(5′)P5(5′)A
A[5']P5[5']A SODIUM SALT
DIADENOSINE PENTAPHOSPHATE SODIUM SALT
Diadenosine pentaphosphate pentasodium
5'-ester with adenosine pentasodium salt
P1,P5-Di(adenosine-5
Diadenosine pentaphosphate pentasodium salt
P1,P5-DI(ADENOSINE-5') PENTAPHOSPHATESOD IUM
P1,P5-DI(ADENOSINE-5') PENTAPHOSPHATE SODIUM SALT
Adenosine 5'-(hexahydrogen pentaphosphate) P''''→
P1,P5-di(adenosine-5')pentaphosphate pentasodium salt 5H2O
Adenosine-5'-pentaphosphateε-5'-adenosyl α,β,γ,δ,ε-pentasodium salt
P1,P5-Di(adenosine-5′) pentaphosphate pentasodium
P1,P5-Di(adenosine-5') pentaphosphate pentasodium salt
Adenosine 5'-(hexahydrogen pentaphosphate) P''''-5'-ester with adenosine pentasodium salt
Adenosine 5'-(hexahydrogen pentaphosphate), 5'->5'-ester with adenosine, pentasodium salt
[EINECS(EC#)]

223-852-7
[Molecular Formula]

C20H24N10Na5O22P5
[MDL Number]

MFCD00077718
[MOL File]

4097-04-5.mol
[Molecular Weight]

1026.28
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: 50 mg/mL
[form ]

powder
[color ]

white to white with yellow cast
[biological source]

synthetic (organic)
[Water Solubility ]

H2O: 50mg/mL
[BRN ]

4949216
[InChIKey]

NNMFUJJMJIYTSP-CSMIRWGRSA-I
Safety DataBack Directory
[WGK Germany ]

3
[F ]

10-21
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

P1,P5-Di(adenosine-5′) pentaphosphate pentasodium salt has been used as:
  • an adenylate kinase (AK) inhibitor in: sarcoma osteogenic (Saos-2) cells
  • mitochondrial lysates during ATP synthesis
  • tetramethylrhodamine methyl ester (TMRM) based membrane potential assay
  • chromoplasts

[General Description]

P1,P5-Di(adenosine-5′) pentaphosphate (Ap5A) is a diadenosine polyphosphate, which has a tail-to-tail dimer structure. Ap5A is synthesized in a twostep process involving the formation of adenosine 5′-tetraphosphate (P4A) from the ATP and trimeta-phosphate (P3). In the second step, P4A is converted to Ap5A. The synthesis of Ap5A requires a pH optimum in the range of 7.5 to 8.5 and is modulated by metal ions.
[Biochem/physiol Actions]

A diadenosine polyphosphate stored in secretory granules of thrombocytes, chromaffin and neuronal cells. After release into the extracellular space, it affects a variety of biological activities in a wide range of target tissues. In the nervous system it acts through various purinergic receptors. It also activates 5′-nucleotidase and inhibits adenosine kinase activity in vitro. Ap5A is metabolized by soluble enzymes in the blood plasma and by membrane-bound ectoenzymes of a number of cell types including endothelial and smooth muscle cells. In cardiac muscle, pM to nM concentrations significantly increase the open-probability of ryanodine-receptor (RyR2) gates, with prolonged action due to slow dissociation from the receptor.
[IC 50]

Human Endogenous Metabolite
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