Substance

ID:357693

P1,P5-Di(adenosine-5′) pentaphosphate trilithium salt

Names and Identifiers
IUPAC name
pentalithium(1+) ion ({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)[({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphinato]oxy}phosphinato)oxy]phosphinate
IUPAC Traditional name
pentalithium(1+) ion Ap5A
Synonyms
Diadenosine pentaphosphate trilithium saltP1,P5-Di(adenosine-5′) pentaphosphate trilithium saltA(5′)P5(5′)A trilithium salt
Registration numbers
MDL Number
CAS Number
EC Number
Properties
Safety Information
MSDS Link
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature
-20°C
German water hazard class
3
Product Information
Impurities
≤5% water
Purity
≥95% (HPLC)
Empirical Formula (Hill Notation)
C20H26Li3N10O22P5
Molecule Details
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.1
Molecular Spectra
No Data Available
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References
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