Compound Identification
SMILES
CNC(=O)[C@H]1S[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2NC
InChIKey
InChIKey=KQEDWUPJFFHILG-QMWPFBOUSA-N
Formula
C12H15ClN6O3S
Mass
358.8
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Nucleoside and nucleotide analogues
Alternative Parents
6-alkylaminopurines 2-halopyrimidines Aminopyrimidines and derivatives Aryl chlorides Imidolactams N-substituted imidazoles Thiolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Secondary carboxylic acid amides Dialkylthioethers Azacyclic compounds Carbonyl compounds Organochlorides Amines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Aryl halide - Pyrimidine - N-substituted imidazole - Aryl chloride - Imidolactam - Thiolane - Heteroaromatic compound - Azole - Imidazole - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Thioether - Dialkylthioether - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.
External Descriptors
Not available