Structure Information
Structure

Compound Identification

SMILES

CCC(=O)O[C@@H]1[C@@H](CO[P@]2(=O)OCC[C@H](O2)C2=CC(Cl)=CC=C2)O[C@H]([C@@H]1OC(=O)CC)N1C=NC(=N1)C(N)=O

InChIKey

InChIKey=NQAGAPDBOSZUOC-OXARTRFTSA-N

Formula

C23H28ClN4O10P

Mass

586.92

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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

Pentose phosphate - Pentose-5-phosphate - N-ribosyl-1,2,4-triazole - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - 2-heteroaryl carboxamide - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Benzenoid - Oxolane - 1,2,4-triazole - Triazole - Heteroaromatic compound - Azole - Primary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organochloride - 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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