Structure Information
Structure

Compound Identification

SMILES

CC(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C(Cl)=C(C=O)C2=CC(Cl)=C(Cl)C=C12

InChIKey

InChIKey=IWWRQXBJTJDXFB-IXYNUQLISA-N

Formula

C16H14Cl3NO6

Mass

422.64

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Indole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Indole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - Indole - Indole or derivatives - Aryl-aldehyde - Aryl chloride - Aryl halide - Monosaccharide - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Tetrahydrofuran - Vinylogous amide - Vinylogous halide - Secondary alcohol - Carboxylic acid ester - 1,2-diol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organochloride - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Aldehyde - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as indole ribonucleosides and ribonucleotides. These are compounds in which the C-1 of a ribosyl (or deoxyribosyl) moiety is linked to the N1-position of an indole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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