Compound Identification
SMILES
CC(=O)N\N=C\C1=C(Cl)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=CC(Cl)=C(Cl)C=C12
InChIKey
InChIKey=YZEOGUDFUWSXFB-XKODNMHPSA-N
Formula
C16H16Cl3N3O5
Mass
436.67
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
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
Glycosylamines Pentoses N-alkylindoles Indoles Substituted pyrroles Aryl chlorides Benzenoids Acetamides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organonitrogen compounds Organic oxides Organochlorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - N-alkylindole - Indole or derivatives - Indole - Monosaccharide - Aryl chloride - Benzenoid - Substituted pyrrole - Aryl halide - Heteroaromatic compound - Acetamide - Oxolane - Pyrrole - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Azacycle - Alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Carbonyl group - Primary alcohol - Organic oxide - Hydrocarbon derivative - 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