Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCCC1=CC=C(CCC(=O)N[C@H](CC(O)=O)C(O)=O)C=C1)N=C2N

InChIKey

InChIKey=NVFHZJAWBNENJM-QNLLXNTNSA-N

Formula

C27H34N8O9

Mass

614.616

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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 - Aspartic acid or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Acyl-homoserine - Acyl-d-homoserine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Benzenoid - Imidolactam - Fatty amide - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Pyrimidine - Fatty acyl - N-substituted imidazole - Imidazole - Heteroaromatic compound - Azole - Oxolane - Amino acid - 1,2-diol - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Carboxylic acid derivative - Carboxylic acid - Carbonyl group - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Amine - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - 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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