Compound Identification
SMILES
NC(=O)N\N=C\C1=C(Cl)N(C2O[C@H](CO)[C@@H](O)[C@H]2O)C2=CC(Cl)=C(Cl)C=C12
InChIKey
InChIKey=ZIMFOVRECXJPIO-ICLWVSMASA-N
Formula
C15H15Cl3N4O5
Mass
437.66
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 Semicarbazones Aryl chlorides Benzenoids Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organochlorides Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - N-alkylindole - Indole - Indole or derivatives - Aryl chloride - Aryl halide - Monosaccharide - Benzenoid - Substituted pyrrole - Semicarbazone - Oxolane - Heteroaromatic compound - Semicarbazide - Pyrrole - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Organohalogen compound - Primary alcohol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - 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