Names | |
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IUPAC name
5′-Adenylic acid
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Systematic IUPAC name
[(2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate | |
Other names
Adenosine 5'-monophosphate
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.000.455 |
KEGG | |
MeSH | Adenosine+monophosphate |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H14N5O7P | |
Molar mass | 347.22 g/mol |
Appearance | white crystalline powder |
Density | 2.32 g/mL |
Melting point | 178 to 185 °C (352 to 365 °F; 451 to 458 K) |
Boiling point | 798.5 °C (1,469.3 °F; 1,071.7 K) |
Acidity (pKa) | 0.9[citation needed], 3.8, 6.1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Adenosine monophosphate (AMP), also known as 5'-adenylic acid, is a nucleotide. AMP consists of a phosphate group, the sugar ribose, and the nucleobase adenine. It is an ester of phosphoric acid and the nucleoside adenosine.[1] As a substituent it takes the form of the prefix adenylyl-.[2]
AMP plays an important role in many cellular metabolic processes, being interconverted to adenosine triphosphate (ATP) and adenosine diphosphate (ADP), as well as allosterically activating enzymes such as myophosphorylase-b. AMP is also a component in the synthesis of RNA.[3] AMP is present in all known forms of life.[4]