Compound Identification
SMILES
COC1=C2C(=O)OC3C(O)C=C4CCN(C)C4C3C2=CC2=C1OCO2
InChIKey
InChIKey=OLGJGNBIBXKMJN-UHFFFAOYSA-N
Formula
C18H19NO6
Mass
345.351
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 Anisoles Alkyl aryl ethers Aralkylamines N-alkylpyrrolidines Lactones Trialkylamines Carboxylic acid esters Amino acids and derivatives Secondary alcohols Azacyclic compounds Oxacyclic compounds Acetals Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - 2-benzopyran - Benzopyran - Isochromane - Indole or derivatives - Benzodioxole - Anisole - Alkyl aryl ether - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Amino acid or derivatives - Lactone - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Carboxylic acid ester - Acetal - Oxacycle - Carboxylic acid derivative - Azacycle - Ether - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Amine - Organic oxygen compound - Organopnictogen compound - Organooxygen compound - Organonitrogen 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