Structure Information
Structure

Compound Identification

SMILES

Cl.CC(C)[C@H](N)C(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=NC(=N1)C(N)=O

InChIKey

InChIKey=BZAMJGAXDMZZKX-JSNLFJDGSA-N

Formula

C13H22ClN5O6

Mass

379.8

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