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Adenosine 2′:3′-cyclic monophosphate sodium salt_Molecular_structure_CAS_37063-35-7)
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Adenosine 2′:3′-cyclic monophosphate sodium salt

Catalog No. A9376 Name Sigma Aldrich
CAS Number 37063-35-7 Website http://www.sigmaaldrich.com
M. F. C10H12N5NaO6P Telephone 1-800-521-8956
M. W. 352.195711 Fax
Purity ≥97% Email
Storage Chembase ID: 133872

SYNONYMS

Title
腺苷 2′:3′-循环磷酸钠盐 钠盐
IUPAC name
4-(6-amino-9H-purin-9-yl)-2-hydroxy-6-(hydroxymethyl)-tetrahydro-2H-1,3,5,2λ5-furo[3,4-d][1,3,2λ5]dioxaphosphol-2-one sodium
IUPAC Traditional name
4-(6-aminopurin-9-yl)-2-hydroxy-6-(hydroxymethyl)-tetrahydro-1,3,5,2λ5-furo[3,4-d][1,3,2λ5]dioxaphosphol-2-one sodium
Synonyms
2′,3′-cAMP sodium salt

DATABASE IDS

CAS Number 37063-35-7
EC Number 253-328-3
MDL Number MFCD00005757
PubChem SID 24891439

PROPERTIES

Purity ≥97%
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Caution
Caution: Do not confuse with the common adenosine 2′(3′)-monophosphate (mixed isomers).
Application
Adenosine 2′,3′-cyclic monophosphate (2′,3′-cAMP) is believed to serve as an extracellular source of adenosine. The release of extracellular 2′,3′-cAMP occurs in response to injury. 2′,3′-cAMP may be used to study the distribution and specificity of its degrading enzymes in the context of unique biological activities. 2′,3′-cAMP may also be used to study apoptosis induced at the level of mitochondrial permeability transition pores. 2′,3′-cAMP is converted into 2′-AMP and 3′-AMP which inhibit proliferation of preglomerular vascular smooth muscle cells and glomerular mesangial cells via A2B receptors.

REFERENCES