Compound Identification
SMILES
CN1CC[C@@H]2C[C@H](OC(=O)C3=CC(C(=O)O[C@H]4C[C@H]5CCN(C)[C@H]5[C@H]5[C@H]4OC(=O)C4=CC6=C(OCO6)C=C54)=C(C)N=C3C)[C@@H]3OC(=O)C4=CC5=C(OCO5)C=C4[C@H]3[C@H]12
InChIKey
InChIKey=CJYOGPFDNAEALZ-BVORSCEZSA-N
Formula
C43H43N3O12
Mass
793.826
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Homolycorine-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Homolycorine-type amaryllidaceae alkaloids
Alternative Parents
Tetracarboxylic acids and derivatives 2-benzopyrans Pyridinecarboxylic acids Benzodioxoles Indoles and derivatives Aralkylamines Methylpyridines Benzenoids N-alkylpyrrolidines Heteroaromatic compounds Carboxylic acid esters Trialkylamines Amino acids and derivatives Lactones Azacyclic compounds Oxacyclic compounds Acetals Organic oxides Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Tetracarboxylic acid or derivatives - Benzopyran - Isochromane - 2-benzopyran - Benzodioxole - Indole or derivatives - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Methylpyridine - Aralkylamine - Pyridine - Benzenoid - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.
External Descriptors
Not available