Structure Information
Structure

Compound Identification

SMILES

CN(CCCCCl)P(=O)(OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC(=N1)C(N)=O)OCC1=CC=CC=C1

InChIKey

InChIKey=RZRJFVUAJYHZQI-ZOOPBYQESA-N

Formula

C20H29ClN5O7P

Mass

517.9

Export to:

JSON SDF CSV

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 - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 2-heteroaryl carboxamide - Phosphoric diester monoamide - Monocyclic benzene moiety - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Benzenoid - Organic phosphoric acid amide - Heteroaromatic compound - 1,2,4-triazole - Triazole - Oxolane - Azole - Secondary alcohol - Primary carboxylic acid amide - 1,2-diol - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxide - Organohalogen compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Alkyl chloride - Organochloride - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organopnictogen compound - Alkyl halide - 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

Previous Back Next