Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCC(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC1=CC=C(CC(=O)NC2=CC=C(CC(=O)NCCNC(C)=O)C=C2)C=C1

InChIKey

InChIKey=FFAWQJFJAOCKKK-URVPBKGTSA-N

Formula

C48H68N8O8

Mass

885.12

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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-glycosyl compound - Glycosyl compound - 6-aminopurine - Pentose monosaccharide - Phenylacetamide - Imidazopyrimidine - Anilide - Purine - Aniline or substituted anilines - N-arylamide - Aminopyrimidine - Fatty acid ester - Monosaccharide - Fatty acyl - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Acetamide - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Amino acid or derivatives - 1,2-diol - Carboxylic acid ester - Carboxamide group - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Azacycle - Oxacycle - Carboxylic acid derivative - Organonitrogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Amine - 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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