Structure Information
Structure

Compound Identification

SMILES

C[C@H](N)C(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=ISYFCRWDMNBLTM-MACXSXHHSA-N

Formula

C13H19N6O8P

Mass

418.303

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Purine ribonucleoside monophosphates

Direct Parent

5'-acylphosphoadenosines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-acylphosphoadenosine - Pentose phosphate - Pentose-5-phosphate - N-glycosyl compound - Alanine or derivatives - Glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Phosphoethanolamine - Monoalkyl phosphate - Acyl phosphate - Aminopyrimidine - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Phosphoric acid ester - N-substituted imidazole - Monosaccharide - Alkyl phosphate - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-acylphosphoadenosines. These are ribonucleoside derivatives containing an adenoside moiety, where the phosphate group is acylated.

External Descriptors

Not available

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