Compound Identification
SMILES
CN(N=O)C(=O)NCC1OC(C(O)C1O)N1C=CC(N)=NC1=O
InChIKey
InChIKey=KAJWGHVYZHHQSN-UHFFFAOYSA-N
Formula
C11H16N6O6
Mass
328.285
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 Aminopyrimidines and derivatives N-methylnitrosoureas Pyrimidones Imidolactams Hydropyrimidines Oxolanes Nitrosamides Heteroaromatic compounds Semicarbazides 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary amines
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - N-methylnitrosourea - Pyrimidone - Hydropyrimidine - Monosaccharide - Nitrosourea - Pyrimidine - Imidolactam - Heteroaromatic compound - Semicarbazide - Nitrosamide - Oxolane - Secondary alcohol - Organic n-nitroso compound - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitroso compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Amine - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxide - Primary amine - Aromatic heteromonocyclic 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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