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Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)N1C=C(N=N1)C1=NC2=C(N=CN=C2N)N1[C@@H]1O[C@@H]2CO[Si](O[Si](O[C@H]2[C@H]1O)(C(C)C)C(C)C)(C(C)C)C(C)C

InChIKey

InChIKey=OOHAJEWFLWNLLX-YUGARCTCSA-N

Formula

C31H46N8O6Si2

Mass

682.929

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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 - Phenyltriazole - Phenyl-1,2,3-triazole - 6-aminopurine - Imidazopyrimidine - Purine - Methoxyaniline - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Aminopyrimidine - Alkyl aryl ether - Imidolactam - Benzenoid - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - 1,2,3-triazole - Triazole - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Azacycle - Organoheterosilane - Organoheterocyclic compound - Organic metalloid salt - Ether - Oxacycle - Amine - Alcohol - Hydrocarbon derivative - Organic metalloid moeity - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Primary amine - Organic nitrogen compound - Organosilicon 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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