Compound Identification
SMILES
OS(=O)(=O)C1CC2C3CCCN4CCCC(CN2C(=O)C1)C34
InChIKey
InChIKey=KWMAUHZNMMZKNJ-UHFFFAOYSA-N
Formula
C15H24N2O4S
Mass
328.43
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 Piperidinones Delta lactams Tertiary carboxylic acid amides Sulfonyls Organosulfonic acids Alkanesulfonic acids Trialkylamines Amino acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Matrine - Quinolizidinone - Naphthyridine - Quinolizidine - Delta-lactam - Piperidinone - Piperidine - Alkanesulfonic acid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Tertiary carboxylic acid amide - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Amino acid or derivatives - Lactam - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Hydrocarbon derivative - Aliphatic 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