Dictionary:
in·o·sin·ic acid (ĭn'ə-sĭn'ĭk, ī'nə-) ![]() |
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| Inosinic acid | |
|---|---|
| Identifiers | |
| CAS number | 131-99-7 |
| PubChem | 8582 |
| MeSH | Inosine+monophosphate |
| Properties | |
| Molecular formula | C10H13N4O8P |
| Molar mass | 348.206 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Inosinic acid or inosine monophosphate (IMP) is a nucleoside monophosphate. Inosinic acid is important in metabolism. It is the ribonucleotide of hypoxanthine and the first nucleotide formed during the synthesis of purine. It is formed by the deamination of adenosine monophosphate, and is hydrolysed to form inosine.
Important derivatives of inosinic acid include purine nucleotides found in nucleic acids and adenosine triphosphate, which is used to store chemical energy in muscle and other tissues.
In the food industry, inosinic acid and its salts such as disodium inosinate are used as flavour enhancers.
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| inosinic | |
| poly I:C (synthetic polymer of inosine) | |
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