Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](OC[C@H]1O[C@H]([C@H](OCCON2C(=O)C3=CC=CC=C3C2=O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC(=O)C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=BWHOMMYROPQBDJ-WDZRAGPMSA-N

Formula

C43H42N6O8Si

Mass

798.928

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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 - Phthalimide - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Isoindolone - Purine - Benzamide - Benzoic acid or derivatives - Isoindole or derivatives - Isoindole - Isoindoline - Imidazopyrimidine - Benzoyl - Alkylarylsilane - Benzenoid - Imidolactam - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Monosaccharide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Silyl ether - Carboxamide group - Organoheterosilane - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organosilicon compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Organic metalloid moeity - 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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