Structure Information
Structure

Compound Identification

SMILES

COCC1=CN=NN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)C2(OS(=O)(=O)C=C2N)[C@H]1O[Si](C)(C)C(C)(C)C

InChIKey

InChIKey=HEFBGDPRGSYXQT-MLJUJGDHSA-N

Formula

C23H44N4O7SSi2

Mass

576.86

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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 - Monosaccharide - Sulfonic acid ester - Organosulfonic acid ester - Azole - 1,2-oxathiole - Organic sulfonic acid or derivatives - Trialkylheterosilane - Organosulfonic acid or derivatives - Tetrahydrofuran - Triazole - 1,2,3-triazole - Heteroaromatic compound - Silyl ether - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Dialkyl ether - Enamine - Organoheterosilane - Ether - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organosilicon compound - Primary amine - Amine - Hydrocarbon derivative - Primary aliphatic amine - Organic salt - Organic oxide - Organic nitrogen compound - Organic oxygen 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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