Compound Identification
SMILES
C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C(=O)N(C)C2=C1NC(N)=NC2=O
InChIKey
InChIKey=FXRRKFRBGDPMRZ-UUOKFMHZSA-N
Formula
C11H15N5O5
Mass
297.271
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
Glycosylamines 6-oxopurines Hypoxanthines Aminopyrimidines and derivatives Pyrimidones N-substituted imidazoles Heteroaromatic compounds Vinylogous amides Oxolanes 1,2-diols Secondary alcohols Ureas Oxacyclic compounds Azacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Pyrimidine - Azole - Oxolane - Imidazole - Vinylogous amide - Heteroaromatic compound - 1,2-diol - Urea - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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