Structure Information
Structure

Compound Identification

SMILES

CC(C)[Si]1(OC[C@H]2O[C@H]([C@H](O)[C@@H]2O[Si](O1)(C(C)C)C(C)C)N1C=NC2=C1N=C(N)N=C2OCCC1=CC=C(C=C1)[N+]([O-])=O)C(C)C

InChIKey

InChIKey=ZEHJGUICSCGZDO-CTDWIVFPSA-N

Formula

C30H46N6O8Si2

Mass

674.902

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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 - Hypoxanthine - Imidazopyrimidine - Nitrobenzene - Purine - Nitroaromatic compound - Alkyl aryl ether - Aminopyrimidine - N-substituted imidazole - Monosaccharide - Primary aromatic amine - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Heteroaromatic compound - Imidazole - Oxolane - Azole - Secondary alcohol - Organic nitro compound - C-nitro compound - Organoheterosilane - Organoheterocyclic compound - Ether - Organic metalloid salt - Oxacycle - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Organic metalloid moeity - Organonitrogen compound - Alcohol - Organooxygen compound - Organic oxygen compound - Primary amine - Organic nitrogen compound - Organopnictogen compound - Amine - Organosilicon compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - 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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