Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C(Br)=CC2=CC(Cl)=C(Cl)C=C12
InChIKey
InChIKey=TYTULTUOEJHWLH-OJAKKHQRSA-N
Formula
C13H12BrCl2NO4
Mass
397.05
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 bromides Aryl chlorides Benzenoids Substituted pyrroles Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Organobromides Primary alcohols Hydrocarbon derivatives Organochlorides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - Pentose monosaccharide - Indole - Indole or derivatives - Aryl bromide - Aryl chloride - Aryl halide - Benzenoid - Substituted pyrrole - Monosaccharide - Heteroaromatic compound - Oxolane - Pyrrole - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organonitrogen compound - Organochloride - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alcohol - Primary 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