Structure Information
Structure

Compound Identification

SMILES

[NH4+].OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCCCCC1=CC=C(C=C1)S([O-])(=O)=O

InChIKey

InChIKey=BGGWHMBTSMMTAM-WQDVGBTGSA-N

Formula

C20H28N6O7S

Mass

496.54

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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 - Phenylbutylamine - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Imidazopyrimidine - Purine - 1-sulfo,2-unsubstituted aromatic compound - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Quaternary ammonium salt - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azole - Heteroaromatic compound - Oxolane - Imidazole - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic zwitterion - Primary alcohol - Organic oxygen compound - Organic salt - Amine - Organonitrogen compound - Organooxygen 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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