Structure Information
Structure

Compound Identification

SMILES

CN(C)C1=CC=CC=C1CN1C=C(CCNC2=NC=NC3=C2N=CN3[C@@H]2O[C@@H]([C@H]3OC(C)(C)O[C@@H]23)C(=O)NC2CC2)C2=CC=CC=C12

InChIKey

InChIKey=BGLADYDPIWTAFZ-YQQRZDPSSA-N

Formula

C35H40N8O4

Mass

636.757

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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 - 6-alkylaminopurine - 6-aminopurine - 3-alkylindole - N-alkylindole - Indole - Indole or derivatives - Purine - Imidazopyrimidine - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Ketal - N-substituted imidazole - Imidolactam - Benzenoid - Substituted pyrrole - Pyrimidine - Monocyclic benzene moiety - Meta-dioxolane - Azole - Imidazole - Heteroaromatic compound - Oxolane - Pyrrole - Secondary carboxylic acid amide - Tertiary amine - Amino acid or derivatives - Carboxamide group - Oxacycle - Organoheterocyclic compound - Azacycle - Acetal - Carboxylic acid derivative - Organooxygen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Amine - Organonitrogen compound - 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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