Compound Identification
SMILES
CC(O)=O.CCC1(O)C(=O)OCC2=C1C=C1C3N=C4C=CC(O)C(CN(C)C)=C4C=C3CN1C2=O
InChIKey
InChIKey=GLKBKYCWKTWPGV-UHFFFAOYSA-N
Formula
C25H29N3O7
Mass
483.521
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
- Class Pyranopyridines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyranopyridines
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyranopyridines
Alternative Parents
Pyridinones Tertiary alcohols Heteroaromatic compounds Trialkylamines Secondary alcohols Amino acids and derivatives Carboxylic acid esters Ketimines Lactams Lactones Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organopnictogen compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds
Molecular Framework
Not available
Substituents
Pyranopyridine - Pyridinone - Pyridine - Heteroaromatic compound - Tertiary alcohol - Amino acid or derivatives - Carboxylic acid ester - Ketimine - Lactam - Lactone - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Imine - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyranopyridines. These are polycyclic aromatic compounds containing a pyran ring fused to a pyridine ring.
External Descriptors
Not available