Compound Identification
SMILES
CCN1N=NC(=N1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N=C2N)N(CO)CCC1=CC=CC=C1
InChIKey
InChIKey=XZYZSWXYIKFJBN-KSVNGYGVSA-N
Formula
C21H26N10O4
Mass
482.505
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 6-aminopurines Dialkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Benzene and substituted derivatives Tetrazoles Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Alkanolamines Azacyclic compounds Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Tetrazole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Alkanolamine - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Primary amine - Amine - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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