Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](OC[C@H]1O[C@H]([C@H](OCCO)[C@H]1O)N1C=NC2=C1NC(N)=NC2=O)(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=JICPENBGQXVPMP-PCEGQDSGSA-N

Formula

C28H35N5O6Si

Mass

565.702

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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 - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Alkylarylsilane - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Silyl ether - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Dialkyl ether - Ether - Organoheterosilane - Primary amine - Organosilicon compound - Hydrocarbon derivative - Organic oxide - Alcohol - Amine - Organic nitrogen compound - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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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