Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OCC1OC(C2OC(C)(C)OC12)N1C=NC(=N1)C(N)=O

InChIKey

InChIKey=MORRJCJYNCYOKM-UHFFFAOYSA-N

Formula

C18H22N4O7S

Mass

438.46

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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-1,2,4-triazole - Benzenesulfonate ester - P-methylbenzenesulfonate - Benzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 2-heteroaryl carboxamide - Toluene - Ketal - Organosulfonic acid ester - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Organosulfonic acid or derivatives - Meta-dioxolane - Organic sulfonic acid or derivatives - Heteroaromatic compound - 1,2,4-triazole - Triazole - Azole - Tetrahydrofuran - Sulfonyl - Primary carboxylic acid amide - Carboxamide group - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organopnictogen 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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