Compound Identification
SMILES
CONC1=NC(Cl)=NC2=C1N=CN2[C@@H]1O[C@H](C=C)[C@@H](O)[C@H]1O
InChIKey
InChIKey=NXIRSLRYLSFOHD-IOSLPCCCSA-N
Formula
C12H14ClN5O4
Mass
327.73
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 Purines and purine derivatives 2-halopyrimidines N-substituted imidazoles Imidolactams Aryl chlorides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds N-organohydroxylamines Azacyclic compounds Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - Imidazopyrimidine - Purine - Halopyrimidine - 2-halopyrimidine - Aryl chloride - Imidolactam - Pyrimidine - N-substituted imidazole - Aryl halide - Heteroaromatic compound - Azole - Oxolane - Imidazole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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