Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OC[C@H]1O[C@H]([C@@H](OCC=C)[C@@H]1O[Si](C)(C)C(C)(C)C)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=AHVFMYOJHCECEX-XBZNOJLSSA-N

Formula

C26H37N5O6SSi

Mass

575.76

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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 - P-methylbenzenesulfonate - Benzenesulfonate ester - N-glycosyl compound - Glycosyl compound - Tosyl compound - Benzenesulfonate - 6-aminopurine - Arylsulfonic acid or derivatives - Purine - Benzenesulfonyl group - Imidazopyrimidine - Aminopyrimidine - Toluene - Monocyclic benzene moiety - Imidolactam - Benzenoid - Organosulfonic acid ester - Primary aromatic amine - N-substituted imidazole - Monosaccharide - Pyrimidine - Azole - Trialkylheterosilane - Imidazole - Heteroaromatic compound - Oxolane - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Silyl ether - Dialkyl ether - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Ether - Oxacycle - Organoheterosilane - Primary amine - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organopnictogen compound - Organic nitrogen compound - Amine - 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

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