Compound Identification
SMILES
NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=NC=C(N1)C=O
InChIKey
InChIKey=KBOQZPODEJKBFW-WOUKDFQISA-N
Formula
C12H15N5O5
Mass
309.282
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Imidazole ribonucleosides and ribonucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Imidazole ribonucleosides and ribonucleotides
Alternative Parents
Glycosylamines Pentoses Aryl-aldehydes Carbonylimidazoles N-substituted imidazoles Aminoimidazoles Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Imidazole ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazole-4-carbonyl group - Aryl-aldehyde - Aminoimidazole - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Aldehyde - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as imidazole ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.
External Descriptors
Not available