Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(COCCO)C=N2.NC(=O)C1=NN(C=N1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey

InChIKey=JJVXTBAWCWLLQC-AFSAJRODSA-N

Formula

C16H23N9O8

Mass

469.415

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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

Not available

Substituents

N-ribosyl-1,2,4-triazole - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Purine - 2-heteroaryl carboxamide - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - 1,2,4-triazole - Triazole - Secondary alcohol - Carboxamide group - Primary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Amine - Primary alcohol - Primary amine - Organonitrogen compound - Organic nitrogen compound - Organooxygen 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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