Compound Identification
SMILES
OCC1OC(C(O)C1O)N1C(Cl)=C(C=O)C2=CC(Cl)=C(Cl)C=C12
InChIKey
InChIKey=QJLFDUROSXZMQK-UHFFFAOYSA-N
Formula
C14H12Cl3NO5
Mass
380.6
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 N-alkylindoles Pentoses Indoles Aryl-aldehydes Substituted pyrroles Aryl chlorides Benzenoids Vinylogous amides Oxolanes Vinylogous halides Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Organic oxides Organochlorides Organonitrogen compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - Pentose monosaccharide - Indole - Indole or derivatives - Aryl-aldehyde - Aryl chloride - Aryl halide - Monosaccharide - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Oxolane - Pyrrole - Vinylogous amide - Vinylogous halide - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - 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