Compound Identification
SMILES
[2H]OC([2H])([2H])[C@@]1([2H])C(=C([2H])[2H])[C@@]([2H])(N2C([2H])=NC3=C2N=C(N([2H])[2H])N([2H])C3=O)C([2H])([2H])[C@]1([2H])O[2H]
InChIKey
InChIKey=QDGZDCVAUDNJFG-QVDNGDBDSA-N
Formula
C12H15N5O3
Mass
292.376
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
Hypoxanthines 6-oxopurines Pyrimidones N-substituted imidazoles Cyclopentanols Vinylogous amides Heteroaromatic compounds Lactams Cyclic alcohols and derivatives Azacyclic compounds Primary amines Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Pyrimidone - Cyclopentanol - N-substituted imidazole - Pyrimidine - Azole - Cyclic alcohol - Imidazole - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Azacycle - Organoheterocyclic compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Alcohol - Primary amine - 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