Name | adenosine 2'-phosphate |
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Synonyms |
Adenosine Monophosphate Hydrate (2'- and 3'- mixture) from Yeast
MFCD00151215 Adenosine 2'-monophosphate Adenylic Acid Hydrate (2'- and 3'- mixture) from Yeast Methionyl adenylate adenosine 2'-monophosphoric acid Adenosine 2'(3')-monophosphate mixed isomers Adenosine 2'-phosphate 2'(3')-AMP Hydrate (2'- and 3'- mixture) from Yeast Methioninyl adenylate 2'-Adenylic acid EINECS 204-990-7 L-METHIONYL ADENYLATE 2'-adenosine monophosphate |
Description | Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite A2A adenosine receptor A2B adenosine receptor |
In Vitro | Adenosine-2'-monophosphate (2'-AMP) (0-100 µM; daily for 4 days) inhibits proliferation of preglomerular vascular smooth muscle cells and glomerular mesangial cells via A2B receptors[1]. Adenosine-2'-monophosphate (30 μM; 24 hours) inhibits LPS induced (100 ng/ml) TNF-α and CXCL10 production in primary murine microglia[1]. |
References |
Density | 2.3±0.1 g/cm3 |
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Boiling Point | 815.5±75.0 °C at 760 mmHg |
Molecular Formula | C10H14N5O7P |
Molecular Weight | 347.221 |
Flash Point | 447.0±37.1 °C |
Exact Mass | 347.063080 |
PSA | 195.88000 |
LogP | -1.74 |
Vapour Pressure | 0.0±3.1 mmHg at 25°C |
Index of Refraction | 1.905 |
Storage condition | −20°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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RIDADR | NONH for all modes of transport |
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WGK Germany | 3 |
RTECS | AU7480300 |
Precursor 8 | |
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DownStream 8 | |