Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](OC[C@H]1O[C@H]([C@H](OC2(C3=CC=CC=C3)C3=CC=CC=C3OC3=CC=CC=C23)[C@@H]1OC1(C2=CC=CC=C2)C2=CC=CC=C2OC2=CC=CC=C12)N1C=NC2=C1N=CN=C2NC(=O)C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=TWSVUPNYZHFPDK-ZHTVQUSFSA-N

Formula

C71H59N5O7Si

Mass

1122.366

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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 - Dibenzopyran - Xanthene - Diaryl ether - Glycosyl compound - N-glycosyl compound - Benzopyran - 1-benzopyran - Benzamide - Benzoic acid or derivatives - Benzylether - Imidazopyrimidine - Purine - Benzoyl - Alkylarylsilane - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Heteroaromatic compound - Azole - Imidazole - Silyl ether - Secondary carboxylic acid amide - Carboxamide group - Organoheterosilane - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic metalloid moeity - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organosilicon compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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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