Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=CC(=CC=C1)[C@@H]1O[C@H](COP(O)(=O)CP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChIKey

InChIKey=VTBRDAVDKUPNCF-YQQLFLHASA-N

Formula

C23H30N6O13P2

Mass

660.47

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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

Not available

Direct Parent

Purine ribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside monophosphate - Phenolic glycoside - C-glycosyl compound - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Benzamide - Imidazopyrimidine - Benzoic acid or derivatives - Bisphosphonate - Purine - Benzoyl - Aminopyrimidine - Pyrimidine - Benzenoid - Imidolactam - Monocyclic benzene moiety - Phosphonic acid ester - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Organophosphonic acid - Organophosphonic acid derivative - Amino acid or derivatives - 1,2-diol - Primary carboxylic acid amide - Secondary alcohol - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Dialkyl ether - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Primary amine - Organophosphorus compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

External Descriptors

Not available

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