Compound Identification
SMILES
CC1=NC=C(COP(O)(O)=O)C(CNOC\C=S(/C)C[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)=C1O
InChIKey
InChIKey=MUYBJLWPDNRHHI-RXMQIEPQSA-N
Formula
C21H30N7O9PS
Mass
587.54
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
Pyridoxamine 5'-phosphates Glycosylamines 6-aminopurines Pentoses Aminopyrimidines and derivatives Hydroxypyridines Methylpyridines Monoalkyl phosphates Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Oxacyclic compounds Thioaldehydes Azacyclic compounds N-organohydroxylamines Hydrocarbon derivatives Primary amines Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Pyridoxamine 5'-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Hydroxypyridine - Aminopyrimidine - Methylpyridine - Monoalkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - N-substituted imidazole - Monosaccharide - Pyrimidine - Pyridine - Heteroaromatic compound - Oxolane - Imidazole - Azole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Thioaldehyde - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Alcohol - Organic nitrogen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organooxygen 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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