Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=GYCVHQYQICRFAX-CKTDUXNWSA-N

Formula

C15H21N7O7

Mass

411.375

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - N-carbamoyl-alpha-amino acid or derivatives - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - N-arylamide - Fatty amide - Fatty acyl - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Tetrahydrofuran - Imidazole - Heteroaromatic compound - Urea - Secondary carboxylic acid amide - Secondary alcohol - Carbonic acid derivative - Carboxamide group - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Alcohol - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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