Structure Information
Structure

Compound Identification

SMILES

CC1(C)CC(CC(C)(C)N1O)NC(=O)CSC1=NC=NC2=C1N=CN2C1OC(CO)C(O)C1O

InChIKey

InChIKey=YYHDRJJZCBPMKH-UHFFFAOYSA-N

Formula

C21H32N6O6S

Mass

496.58

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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 - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Alkylarylthioether - Monosaccharide - N-substituted imidazole - Piperidine - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Tetrahydrofuran - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Sulfenyl compound - Thioether - Carboxylic acid derivative - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Organopnictogen 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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