Compound Identification
SMILES
CCN1N=NC(=N1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(CNS(=O)(=O)CC(C)C)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1
InChIKey
InChIKey=JUAMPWCKIMEGCG-OVDFTCDZSA-N
Formula
C31H38N10O5S
Mass
662.77
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
Diphenylmethanes 6-alkylaminopurines Glycosylamines Aminopyrimidines and derivatives Organosulfonamides Organic sulfonamides Imidolactams N-substituted imidazoles Tetrazoles Aminosulfonyl compounds Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Amines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5'-deoxyribonucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Imidolactam - Organosulfonic acid or derivatives - Azole - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Tetrazole - Oxolane - Sulfonyl - Heteroaromatic compound - Imidazole - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Alcohol - Organonitrogen compound - Organic nitrogen compound - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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