A[5']P5[5']A SODIUM SALT
A[5']P5[5']A SODIUM SALT Basic information
- Product Name:
- A[5']P5[5']A SODIUM SALT
- Synonyms:
-
- A[5']P5[5']A SODIUM SALT
- P1,P5-DI(ADENOSINE-5') PENTAPHOSPHATE SODIUM SALT
- Adenosine 5'-(hexahydrogen pentaphosphate), 5'->5'-ester with adenosine, pentasodium salt
- P1,P5-DI(ADENOSINE-5') PENTAPHOSPHATESOD IUM
- P1,P5-di(adenosine-5')pentaphosphate pentasodium salt 5H2O
- Adenosine-5'-pentaphosphateε-5'-adenosyl α,β,γ,δ,ε-pentasodium salt
- A(5′)P5(5′)A
- Diadenosine pentaphosphate pentasodium salt
- CAS:
- 4097-04-5
- MF:
- C20H24N10Na5O22P5
- MW:
- 1026.28
- EINECS:
- 223-852-7
- Mol File:
- 4097-04-5.mol
A[5']P5[5']A SODIUM SALT Chemical Properties
- storage temp.
- -20°C
- solubility
- H2O: 50 mg/mL
- form
- powder
- color
- white to white with yellow cast
- BRN
- 4949216
Safety Information
- WGK Germany
- 3
- F
- 10-21
MSDS
- Language:English Provider:SigmaAldrich
A[5']P5[5']A SODIUM SALT Usage And Synthesis
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.
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