Compound Identification
SMILES
CCCCCCCCCC1=C(N)NC(=O)C2=C1N(C=N2)[C@H]1C[C@H](O)[C@@H](CO)O1
InChIKey
InChIKey=ZIQRWBFWCZVDFI-ARFHVFGLSA-N
Formula
C20H32N4O4
Mass
392.5
Taxonomic Classification
Taxonomy Tree
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides
Alternative Parents
Imidazopyridinones Imidazo-[4,5-c]pyridines Pyridinones Aminopyridines and derivatives N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Secondary alcohols Lactams Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Imidazole[4,5-c]pyridine ribonucleoside,ribonucleotide or analogue - Imidazopyridinone - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - Pyridinone - N-substituted imidazole - Pyridine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Oxolane - Lactam - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Primary amine - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole[4,5-c]pyridine ring system. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
External Descriptors
Not available