Structure Information
Structure

Compound Identification

SMILES

COC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(CNS(=O)(=O)CC(C)(C)C)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=IYPCMZQJQWIRPD-WFCSWSGSSA-N

Formula

C31H40N6O6S

Mass

624.76

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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 - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Aminopyrimidine - Benzenoid - N-substituted imidazole - Imidolactam - Organosulfonic acid amide - Monosaccharide - Organic sulfonic acid amide - Monocyclic benzene moiety - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Aminosulfonyl compound - Oxolane - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Dialkyl ether - Ether - Oxacycle - Azacycle - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Amine - Organic nitrogen compound - Alcohol - Organic oxygen 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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