Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=CN(N=N1)C1OC(CO[Si](C)(C)C(C)(C)C)C2(OS(=O)(=O)C=C2N)C1O[Si](C)(C)C(C)(C)C

InChIKey

InChIKey=RRAOIANRLSFYQG-UHFFFAOYSA-N

Formula

C24H44N4O8SSi2

Mass

604.87

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Triazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Triazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-ribosyl-1,2,3-triazole - N-glycosyl compound - Glycosyl compound - Organosulfonic acid ester - Monosaccharide - Sulfonic acid ester - 1,2,3-triazole - Heteroaromatic compound - 1,2-oxathiole - Oxolane - Organic sulfonic acid or derivatives - Vinylogous amide - Azole - Organosulfonic acid or derivatives - Trialkylheterosilane - Silyl ether - Carboxylic acid ester - Carboxylic acid derivative - Enamine - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic metalloid moeity - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organonitrogen compound - Organooxygen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organosilicon compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as triazole ribonucleosides and ribonucleotides. These are nucleoside derivatives containing a ribose (or deoxyribose) moiety which is N-glycosylated to a triazole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

Previous Back Next