Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1C[C@@H](C=C1)C([N+]([O-])=O)S(=O)(=O)C1=CC=CC=C1
InChIKey
InChIKey=DFUWWRLTPQRLFE-XGDHHHFCSA-N
Formula
C17H16N6O4S
Mass
400.41
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-aminopurines Benzenesulfonyl compounds Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Sulfones Heteroaromatic compounds C-nitro compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Hydrocarbon derivatives Organic salts Organic zwitterions Primary amines Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-aminopurine - Benzenesulfonyl group - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Sulfone - Sulfonyl - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic oxoazanium - Azacycle - Organic salt - Organic zwitterion - Organic oxygen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Organosulfur compound - Primary amine - Organic oxide - Organic nitrogen 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