Compound Identification
SMILES
COC1CC2N(C)C(=O)C3N(CCC4=CC=C(O)C=C4)C(=O)C4=CC5(O)OCOC5(O)C=C4C23C=C1
InChIKey
InChIKey=YEQOPRLZTKWWMW-UHFFFAOYSA-N
Formula
C26H28N2O8
Mass
496.516
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Amaryllidaceae alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Plicamine-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Plicamine-type amaryllidaceae alkaloids
Alternative Parents
Isoquinolones and derivatives Azaspirodecane derivatives Alpha amino acids and derivatives Indoles and derivatives Piperidinones Delta lactams 1-hydroxy-2-unsubstituted benzenoids Pyrrolidine-2-ones Benzene and substituted derivatives N-alkylpyrrolidines Tertiary carboxylic acid amides 1,3-dioxolanes Hemiacetals Dialkyl ethers Oxacyclic compounds Azacyclic compounds Acetals Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Plicamine alkaloid skeleton - Isoquinolone - Alpha-amino acid or derivatives - Azaspirodecane - Indole or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Delta-lactam - Phenol - Piperidinone - Benzenoid - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Monocyclic benzene moiety - Piperidine - Meta-dioxolane - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Hemiacetal - Lactam - Azacycle - Oxacycle - Ether - Dialkyl ether - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as plicamine-type amaryllidaceae alkaloids. These are dinitrogenous Amaryllidaceae alkaloids derived from tazettine-type alkaloids, by replacement of the oxygen atom at the C6 by a nitrogen atom, which is in turn substituted with a 4-hydroxyphenethyl unit. In addition, all alkaloids of this minor subgroup have an amide group on the C12.
External Descriptors
Not available