Compound Identification
SMILES
[H]C(C)(O)CC(=O)OC1([H])CC2([H])CCN(C)C2([H])C2([H])C3=CC4=C(OCO4)C=C3C(=O)OC12[H]
InChIKey
InChIKey=QYVZOJWDWWFSQK-UHFFFAOYSA-N
Formula
C21H25NO7
Mass
403.431
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
2-benzopyrans Benzodioxoles Indoles and derivatives Aralkylamines Beta hydroxy acids and derivatives Fatty acid esters Benzenoids Dicarboxylic acids and derivatives N-alkylpyrrolidines Carboxylic acid esters Trialkylamines Secondary alcohols Amino acids and derivatives Lactones Acetals Oxacyclic compounds Azacyclic compounds Organic oxides Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Benzodioxole - Beta-hydroxy acid - Fatty acid ester - Aralkylamine - Dicarboxylic acid or derivatives - N-alkylpyrrolidine - Benzenoid - Hydroxy acid - Fatty acyl - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactone - Carboxylic acid ester - Amino acid or derivatives - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - 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