Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP([O-])(=O)OC=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=WEMRJXXSNYFBKN-IOSLPCCCSA-M

Formula

C11H13N5O8P

Mass

374.226

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