Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)N1C=NC2=C(CCNC3=NC(=O)N(C=C3)[C@@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)N=C(N)N=C12

InChIKey

InChIKey=UHDLGEJLRJSKJO-NJNHCMIBSA-N

Formula

C57H112N8O9Si6

Mass

1222.08

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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 - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Oxolane - Trialkylheterosilane - Silyl ether - Organoheterocyclic compound - Organoheterosilane - Organic metalloid salt - Oxacycle - Azacycle - Organosilicon compound - Organic metalloid moeity - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic oxide - Primary amine - 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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