Structure Information
Structure

Compound Identification

SMILES

CC(C)[Si]1(OC[C@H]2O[C@H]([C@H](OCC=C)[C@@H]2O[Si](O1)(C(C)C)C(C)C)N1C=NC2=C1N=CN=C2NC(=O)C(C)(C)C)C(C)C

InChIKey

InChIKey=BLANTYJMVLFJMD-ZYWWQZICSA-N

Formula

C30H51N5O6Si2

Mass

633.937

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