Compound Identification
SMILES
CCOC(=O)C1=CN=C(N1)[C@@H]1O[C@H](COCC2=CC=CC=C2)[C@@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1
InChIKey
InChIKey=HAGIOCBRSCTZKE-SKKKGAJSSA-N
Formula
C32H34N2O6
Mass
542.632
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
C2-linked imidazole ribonucleosides and ribonucleotides
Intermediate Tree Nodes
Not available
Direct Parent
C2-linked imidazole ribonucleosides and ribonucleotides
Alternative Parents
C-glycosyl compounds Pentoses Benzylethers Carbonylimidazoles Oxolanes Heteroaromatic compounds Carboxylic acid esters Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
C2-linked imidazole ribonucleoside - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Benzylether - Imidazole-4-carbonyl group - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Azole - Heteroaromatic compound - Oxolane - Imidazole - Carboxylic acid ester - Oxacycle - Carboxylic acid derivative - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as c2-linked imidazole ribonucleosides and ribonucleotides. These are nucleoside and nucleotide analogues with a structure that consists of an imidazole ring system which is substituted at the C2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
External Descriptors
Not available