Compound Identification
SMILES
CO[C@@H]1[C@@H](CO)O[C@H]([C@@H]1O)N1C=NC2=C1N=C1N(C)C=NN1C2=O
InChIKey
InChIKey=JHQHYEIJOGMDQR-WOUKDFQISA-N
Formula
C13H16N6O5
Mass
336.308
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
Glycosylamines 6-oxopurines Hypoxanthines Triazolopyrimidines Pyrimidones N-substituted imidazoles Monosaccharides Vinylogous amides Triazoles Oxolanes Heteroaromatic compounds Secondary alcohols Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Triazolopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Vinylogous amide - Oxolane - Heteroaromatic compound - 1,2,4-triazole - Triazole - Lactam - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Dialkyl ether - Ether - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Primary alcohol - Alcohol - Organic oxygen 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