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@]11OS(=O)(=O)C=C1N)N1C=C(N=N1)C(N)=O

InChIKey

InChIKey=HRZLJIOJVATSPB-ZRAXVTTISA-N

Formula

C22H41N5O7SSi2

Mass

575.83

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

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