Compound Identification
SMILES
O[C@@H]1[C@@H](CCC(=O)C2=CC(=CC=C2)C([O-])=O)O[C@@H]([C@@H]1O)N1C=NC2=C1NC=NC2=O
InChIKey
InChIKey=VEDWXCWBMDQNCV-DRRHNWJESA-M
Formula
C19H17N4O7
Mass
413.367
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class 5'-deoxyribonucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
5'-deoxyribonucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
5'-deoxyribonucleosides
Alternative Parents
Alkyl-phenylketones Butyrophenones Glycosylamines 6-oxopurines Hypoxanthines Benzoic acids Benzoyl derivatives Aryl alkyl ketones Pyrimidones N-substituted imidazoles Monosaccharides Heteroaromatic compounds Oxolanes Vinylogous amides 1,2-diols Secondary alcohols Carboxylic acid salts Carboxylic acids Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic anions
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Alkyl-phenylketone - N-glycosyl compound - Glycosyl compound - Butyrophenone - 6-oxopurine - Hypoxanthine - Phenylketone - Imidazopyrimidine - Benzoic acid or derivatives - Benzoic acid - Purine - Benzoyl - Aryl alkyl ketone - Aryl ketone - Pyrimidone - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Heteroaromatic compound - Imidazole - Azole - Oxolane - Vinylogous amide - Carboxylic acid salt - 1,2-diol - Ketone - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organonitrogen compound - Organic anion - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
External Descriptors
Not available