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5-Aminoimidazole-4-carboxamide-1-β-D-ribofuranoside-13C2,15N_Molecular_structure_CAS_)
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5-Aminoimidazole-4-carboxamide-1-β-D-ribofuranoside-13C2,15N

Catalog No. A611702 Name Toronto Research Chemicals
CAS Number Website http://www.trc-canada.com
M. F. C9H14N4O5 Telephone +1 (416) 665-9696
M. W. 261.20997857 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage -20°C Freezer Chembase ID: 160202

SYNONYMS

IUPAC name
5-amino-1-[(2R,3S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl](4,5-13C2,3-15N)-1H-imidazole-4-carboxamide
IUPAC Traditional name
5-amino-1-[(2R,3S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl](4,5-13C2,3-15N)imidazole-4-carboxamide
Synonyms
GP 1-110-13C2,15N
5-Amino-4-imidazolecarboxamide Riboside-13C2,15N
Arasine-13C2,15N
AICAR-13C2,15N
5-Aminoimidazole-4-carboxamide-1-β-D-ribofuranoside-13C2,15N
Acadesine-13C2,15N
NSC 105823-13C2,15N

DATABASE IDS

PROPERTIES

Certificate of Analysis Download
Apperance White Solid
Melting Point 187-192°C
Solubility DMSO
Solubility Methanol
MSDS Link Download
Storage Condition -20°C Freezer

DETAILS

Description (English)
A labelled nucleoside analogue that is able to enter nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP breakdown. Adenosine-regulating agents (ARAs) have been recognized for therapeutic potential in myocardi

REFERENCES

  • Mullane, K., et al.: Trends Cardiovasc Med., 3, 227 (1993)
  • Browne, G.J., et al.: J. Biol. Chem., 279, 13, 12220 (2004)