Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](O[C@@H]2CO[Si](O[Si](O[C@@H]12)(C(C)C)C(C)C)(C(C)C)C(C)C)N1C=NC2=C1NC(NC(=O)C(C)C)=NC2=O

InChIKey

InChIKey=UOKIEARTPZHFMJ-RKCWLVDCSA-N

Formula

C27H47N5O7Si2

Mass

609.871

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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 - Imidazopyrimidine - Purine - N-arylamide - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Organoheterocyclic compound - Organic metalloid salt - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterosilane - Organosilicon compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Carbonyl group - 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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