Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=NN(C=N1)[C@@H]1O[C@H](COC(=O)[C@H]2C[C@@H](O)CN2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=ZMYRLEMUBAWPJH-GDQZAIIHSA-N

Formula

C13H19N5O7

Mass

357.323

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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 heteromonocyclic compounds

Substituents

N-ribosyl-1,2,4-triazole - Alpha-amino acid ester - Proline or derivatives - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Pentose monosaccharide - 2-heteroaryl carboxamide - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Monosaccharide - Azole - Heteroaromatic compound - Oxolane - Pyrrolidine - Triazole - 1,2,4-triazole - Secondary alcohol - Amino acid or derivatives - 1,2-aminoalcohol - Carboxamide group - Carboxylic acid ester - 1,2-diol - Primary carboxylic acid amide - Monocarboxylic acid or derivatives - Azacycle - Oxacycle - Secondary aliphatic amine - Organoheterocyclic compound - Carboxylic acid derivative - Secondary amine - Hydrocarbon derivative - Carbonyl group - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Alcohol - Organic oxide - Organic oxygen compound - Aromatic heteromonocyclic 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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