Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=VAWJHLCGHNFLHF-WFMPWKQPSA-N

Formula

C14H21N6O8PS

Mass

464.39

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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 - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - Hydroxy fatty acid - Aminopyrimidine - Thia fatty acid - Phosphoric monoester monoamide - Organic phosphoric acid derivative - Pyrimidine - N-substituted imidazole - Phosphoric acid ester - Monosaccharide - Organic phosphoric acid amide - Imidolactam - Fatty acyl - Heteroaromatic compound - Oxolane - Imidazole - Azole - 1,2-diol - Secondary alcohol - Amino acid or derivatives - Amino acid - Alkylthiol - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Carbonyl group - Alcohol - Organic oxygen compound - Organic oxide - Amine - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - 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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