Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CN=NN1[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@]2(OS(=O)(=O)C=C2NC(C)=O)[C@H]1O[Si](C)(C)C(C)(C)C

InChIKey

InChIKey=LSWAAHIEFHSEIA-FBROZUCGSA-N

Formula

C25H44N4O9SSi2

Mass

632.88

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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 - Sulfonic acid ester - Organosulfonic acid ester - Monosaccharide - Azole - Organosulfonic acid or derivatives - Triazole - 1,2,3-triazole - Heteroaromatic compound - 1,2-oxathiole - Oxolane - Acetamide - Trialkylheterosilane - Methyl ester - Organic sulfonic acid or derivatives - Silyl ether - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Carboxylic acid derivative - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic metalloid moeity - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - 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

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