Inosinic acid

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Inosinic acid
2D structure for Inosinic acid
Chemical Name [3,4-dihydroxy-5-(6-hydroxypurin-9-yl)-oxolan-2-yl]methoxyphosphonic acid
Chemical Formula C10H13N4O8P
CAS Number 131-99-7
Chemical Information HMDB00175
Biochemical Taxonomy

  • Nucleotides

Functional Taxonomy Not Available
Nutritional Taxonomy Not Available
Metabolic Pathways

  • Alanine and Aspartate Metabolism
  • Nicotinate and Nicotinamide Metabolism
  • Purine Metabolism
  • Starch and Sucrose Metabolism

Biofluid Location

  • Blood
  • Cellular Cytoplasm
  • Cerebrospinal Fluid (CSF)

Tissue Location

  • All Tissues

Normal Biofluid Concentrations

  • Blood: 63.0 +/- 41.0 uM
  • Cellular Cytoplasm: 10 uM
  • Cerebrospinal Fluid (CSF): 3.19 (0.00 +/- 19.70) uM

Normal Tissue Concentrations Not Available
Diseases / Conditions Related to Nutrition

  • Complex febrile seizures
  • Simple ffebrile seizures

Other (Monogenic Disorders) Not Available
Abnormal Biofluid Concentrations

  • Cerebrospinal Fluid (CSF) (Complex febrile seizures): 2.48 (0.00 +/- 27.20) uM
  • Cerebrospinal Fluid (CSF) (Simple ffebrile seizures): 2.31(0.00-41.40) uM

Abnormal Tissue Concentrations Not Available
Physiological Processes Not Available
Authors:
Affiliations:

Contents

Introduction

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A purine nucleotide which has hypoxanthine as the base and one phosphate group esterified to the sugar moiety. Inosinic acid is a nucleotide present in muscle and other tissues. It is formed by the deamination of AMP and when hydrolysed produces inosine. Inosinic acid is the ribonucleotide of hypoxanthine and is the first compound formed during the synthesis of purine. (Wikipedia)

Biological Function

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Catabolism

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Diseases / Conditions Related to Nutrition

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  • Complex febrile seizures
  • Simple ffebrile seizures

Other (Monogenic) Disorders

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Nutritional Information

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Drivers for biological variation

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Vulnerable groups

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Other resources

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Links

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