Structure Information
Structure

Compound Identification

SMILES

CN(C)\C=N\C1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](CO[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)[C@@H](OC(=O)CCC(C)=O)[C@H]1OC(=O)CCC(C)=O

InChIKey

InChIKey=VLBANLIZRYRFAA-GPQWOTRVSA-N

Formula

C39H48N6O9Si

Mass

772.931

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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 - N-glycosyl compound - Glycosyl compound - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Gamma-keto acid - Pyrimidone - Alkylarylsilane - Fatty acid ester - Dicarboxylic acid or derivatives - Keto acid - Fatty acyl - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Silyl ether - Carboxylic acid ester - Ketone - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Formamidine - Carboxylic acid amidine - Carboxylic acid derivative - Organoheterosilane - Amidine - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organosilicon compound - Organonitrogen compound - Organic oxygen compound - Organic metalloid moeity - Carbonyl group - Organic nitrogen 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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