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(Cl)N=C2NCC1=CC(I)=CC=C1)C(C)C

InChIKey

InChIKey=LUAJXYDIXCJGPH-ZYWWQZICSA-N

Formula

C29H43ClIN5O5Si2

Mass

760.22

Export to:

JSON SDF CSV

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-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - 2-halopyrimidine - Halobenzene - Halopyrimidine - Iodobenzene - Secondary aliphatic/aromatic amine - Aryl chloride - Aryl halide - Aryl iodide - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Azole - Tetrahydrofuran - Heteroaromatic compound - Imidazole - Secondary alcohol - Secondary amine - Organoheterocyclic compound - Organoheterosilane - Organic metalloid salt - Azacycle - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Organohalogen compound - Alcohol - Amine - Organochloride - Organic salt - Organoiodide - Organonitrogen compound - Organosilicon 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

Previous Back Next