Structure Information
Structure

Compound Identification

SMILES

CCOC(OCC)C1=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=RJNCUZQJIYVUCB-CHJIAWOGSA-N

Formula

C26H50N4O8SSi2

Mass

634.94

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