Compound Identification
SMILES
O[C@@H]1[C@@H](CCl)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2NN1CCC(CC1)SC1=CC=CC=C1
InChIKey
InChIKey=ZWMXNEWPLAOIAZ-WVSUBDOOSA-N
Formula
C21H24Cl2N6O3S
Mass
511.42
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 Pentoses Purines and purine derivatives Thiophenol ethers 2-halopyrimidines Alkylarylthioethers Aryl chlorides Benzene and substituted derivatives Piperidines Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Sulfenyl compounds Azacyclic compounds Alkylhydrazines Oxacyclic compounds Hydrocarbon derivatives Alkyl chlorides Organochlorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - 2-halopyrimidine - Halopyrimidine - Alkylarylthioether - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Piperidine - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Oxolane - Azole - Imidazole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Sulfenyl compound - Azacycle - Thioether - Oxacycle - Alkylhydrazine - Alkyl chloride - Hydrazine derivative - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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