Adenosine-2'-monophosphate structure
|
Common Name | Adenosine-2'-monophosphate | ||
---|---|---|---|---|
CAS Number | 130-49-4 | Molecular Weight | 347.221 | |
Density | 2.3±0.1 g/cm3 | Boiling Point | 815.5±75.0 °C at 760 mmHg | |
Molecular Formula | C10H14N5O7P | Melting Point | N/A | |
MSDS | USA | Flash Point | 447.0±37.1 °C |
Use of Adenosine-2'-monophosphateAdenosine-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]. |
Name | adenosine 2'-phosphate |
---|---|
Synonym | More Synonyms |
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]. |
---|---|
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 |
---|---|
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
|
RIDADR | NONH for all modes of transport |
---|---|
WGK Germany | 3 |
RTECS | AU7480300 |
Precursor 8 | |
---|---|
DownStream 8 | |
The RimL transacetylase provides resistance to translation inhibitor microcin C.
J. Bacteriol. 196(19) , 3377-85, (2014) Peptide-nucleotide antibiotic microcin C (McC) is produced by some Escherichia coli strains. Inside a sensitive cell, McC is processed, releasing a nonhydrolyzable analog of aspartyl-adenylate, which ... |
|
Aprataxin resolves adenylated RNA-DNA junctions to maintain genome integrity.
Nature 506(7486) , 111-5, (2014) Faithful maintenance and propagation of eukaryotic genomes is ensured by three-step DNA ligation reactions used by ATP-dependent DNA ligases. Paradoxically, when DNA ligases encounter nicked DNA struc... |
|
Eukaryotic elongation factor 2 kinase regulates the cold stress response by slowing translation elongation.
Biochem. J. 465(2) , 227-38, (2015) Cells respond to external stress conditions by controlling gene expression, a process which occurs rapidly via post-transcriptional regulation at the level of protein synthesis. Global control of tran... |
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 |