Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@H](O[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)[C@@H](CON=C)O[C@H]1N1C=NC2=C1N=CN=C2NC(=O)C1=CC=CC=C1

InChIKey

InChIKey=MCCBNMBGTLZLCV-WIFIACMTSA-N

Formula

C35H38N6O5Si

Mass

650.811

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