Compound Identification
SMILES
C[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N)N=C2S(N)=O
InChIKey
InChIKey=WRTXNEGYBLKACV-PCOJCEOPSA-N
Formula
C10H14N6O4S
Mass
314.32
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 Aminopyrimidines and derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Sulfinic acid amides Secondary alcohols Aminosulfinyl compounds 1,2-diols Oxacyclic compounds Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Sulfinic acid amide - Secondary alcohol - Aminosulfinyl compound - Sulfinic acid derivative - 1,2-diol - Azacycle - Oxacycle - Organoheterocyclic compound - Sulfinyl compound - Primary amine - Amine - Hydrocarbon derivative - Alcohol - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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