Compound Identification
SMILES
O=C(C1CCC2C3CCCN4CCCC(CN2C1=O)C34)C1=CC=CO1
InChIKey
InChIKey=GPFWRMZTMORDJV-UHFFFAOYSA-N
Formula
C20H26N2O3
Mass
342.439
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Matrine alkaloids
-
Class
Lupin alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Lupin alkaloids
Subclass
Matrine alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Matrine alkaloids
Alternative Parents
Quinolizidinones Naphthyridines Aryl alkyl ketones Piperidinones Delta lactams 1,3-dicarbonyl compounds Tertiary carboxylic acid amides Heteroaromatic compounds Furans Trialkylamines Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Matrine - Quinolizidinone - Naphthyridine - Quinolizidine - Aryl alkyl ketone - Aryl ketone - Delta-lactam - Piperidinone - Piperidine - 1,3-dicarbonyl compound - Furan - Heteroaromatic compound - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Ketone - Lactam - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as matrine alkaloids. These are lupin alkaloids with a structure based on the matrine skeleton, a four-ring skeleton that based on a saturated dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10-one skeleton.
External Descriptors
Not available