Structure Information
Structure

Compound Identification

SMILES

NC1=NC(SCCNC(=O)CCC2=CC(I)=C(O)C=C2)=NC2=C1N=CN2C1OC(CO)C(O)C1O

InChIKey

InChIKey=HMDUDYOOQWFSCQ-UHFFFAOYSA-N

Formula

C21H25IN6O6S

Mass

616.43

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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 - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - 2-halophenol - 2-iodophenol - Aminopyrimidine - 1-hydroxy-2-unsubstituted benzenoid - Halobenzene - Iodobenzene - Phenol - Alkylarylthioether - Fatty amide - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Aryl iodide - Aryl halide - Benzenoid - Imidolactam - Fatty acyl - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Tetrahydrofuran - Carboxamide group - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Sulfenyl compound - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Azacycle - Thioether - Primary amine - Organic oxygen compound - Alcohol - Amine - Organopnictogen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organoiodide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - 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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