Compound Identification
SMILES
CN(C)\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=SLOWIEFADADHMU-TXMPWXBFSA-N
Formula
C16H18Cl3N3O4
Mass
422.69
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 Substituted pyrroles Benzenoids Aryl chlorides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Hydrazones Azacyclic compounds Organochlorides 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 chloride - Aryl halide - Monosaccharide - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Oxolane - Pyrrole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrazone - Alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - 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