Compound Identification
SMILES
NC1=NC(=O)C2=C(NC(CSC[C@H]3OC([C@H](O)[C@@H]3O)N3C=NC4=C3N=CN=C4N)=C2)N1
InChIKey
InChIKey=SQLQZCWJQHPUAV-ITAOHXQZSA-N
Formula
C17H19N9O4S
Mass
445.46
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Nucleosides, nucleotides, and analogues
-
Class
5'-deoxyribonucleosides
- Subclass 5'-deoxy-5'-thionucleosides
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Class
5'-deoxyribonucleosides
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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-aminopurines Pentoses Pyrrolo[2,3-d]pyrimidines Aminopyrimidines and derivatives Pyrimidones Substituted pyrroles N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Vinylogous amides 1,2-diols Secondary alcohols Oxacyclic compounds Sulfenyl compounds Dialkylthioethers Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxy-5'-thionucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Imidazopyrimidine - Purine - Pyrrolopyrimidine - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Substituted pyrrole - Imidolactam - Vinylogous amide - Pyrrole - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Dialkylthioether - Azacycle - Sulfenyl compound - Oxacycle - Thioether - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organosulfur compound - Primary amine - Alcohol - 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