Compound Identification
SMILES
NC1=NC2=C(NC(N)=NC2=O)N1C1OC(CSC2=CC=CC=C2)C(O)C1O
InChIKey
InChIKey=PXTVGMNFEPZMRB-UHFFFAOYSA-N
Formula
C16H18N6O4S
Mass
390.42
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
5'-deoxyribonucleosides
- Subclass 5'-deoxy-5'-thionucleosides
-
Class
5'-deoxyribonucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
5'-deoxyribonucleosides
Subclass
5'-deoxy-5'-thionucleosides
Intermediate Tree Nodes
Not available
Direct Parent
5'-deoxy-5'-thionucleosides
Alternative Parents
Glycosylamines 6-oxopurines Pentoses Hypoxanthines Thiophenol ethers Pyrimidones Alkylarylthioethers Aminopyrimidines and derivatives Aminoimidazoles N-substituted imidazoles Benzene and substituted derivatives Vinylogous amides Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxy-5'-thionucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Pyrimidone - Alkylarylthioether - Benzenoid - Aminoimidazole - Monocyclic benzene moiety - Monosaccharide - Pyrimidine - N-substituted imidazole - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - 1,2-diol - Secondary alcohol - Azacycle - Oxacycle - Organoheterocyclic compound - Thioether - Sulfenyl compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Amine - Organosulfur compound - Organic nitrogen compound - Organonitrogen compound - Primary amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 5'-deoxy-5'-thionucleosides. These are 5'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.
External Descriptors
Not available