C145
2-Chloroadenosine triphosphate tetrasodium hydrate
solid, ≥90% (HPLC)
Synonym(s):
2-Chloro-ATP tetrasodium hydrate, 2-Chloroadenosine 5′-triphosphate tetrasodium hydrate
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About This Item
Empirical Formula (Hill Notation):
C10H11ClN5Na4O13P3 · xH2O
Molecular Weight:
629.55 (anhydrous basis)
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
SMILES string
O.[Na+].[Na+].[Na+].[Na+].Nc1nc(Cl)nc2n(cnc12)[C@@H]3O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]3O
assay
≥90% (HPLC)
form
solid
storage condition
desiccated
color
white
solubility
H2O: soluble
εmax
17,800 at 273 nm in methanol, 20,900 at 215 nm in methanol
storage temp.
−20°C
Gene Information
Biochem/physiol Actions
P2Y purinoceptor agonist.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Neuro-modulatory roles of purine nucleosides and nucleotides: their receptors and ligands.
Williams, et al.
Neurotransmissions, 6 (1990)
Three new adenosine triphosphate analogs. Synthesis and effects on isolated gut.
G R Gough et al.
Journal of medicinal chemistry, 16(10), 1188-1190 (1973-10-01)
G Burnstock et al.
British journal of pharmacology, 79(4), 907-913 (1983-08-01)
ATP, 2-chloro-ATP, 2-methylthio-ATP, and their unnatural L-enantiomers, were synthesized and their effects tested on the guinea-pig taenia coli and urinary bladder, and the stimulated frog ventricle. The potent P2-purinoceptor agonists, 2-chloro-ATP and 2-methylthio-ATP were, respectively, 30 and 200 times more
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