Structure Information
Structure

Compound Identification

SMILES

COCC1OC(C(O)C1O)N1C=NC2=C1N=C(CNS(=O)(=O)C1=CC=C(C=C1)C1CCNCC1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=QAJKBIYMAXPTOI-UHFFFAOYSA-N

Formula

C37H43N7O6S

Mass

713.85

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