Compound Identification
SMILES
COC1CC2N(C)C(=O)C3N(CCC4=CC=C(O)C=C4)C(=O)C4CC5=C(OCO5)C=C4C23C=C1
InChIKey
InChIKey=SNGIERBGYISDIX-UHFFFAOYSA-N
Formula
C26H28N2O6
Mass
464.518
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
Alpha amino acids and derivatives Azaspirodecane derivatives Indoles and derivatives Piperidinones 1-hydroxy-2-unsubstituted benzenoids Delta lactams Pyrrolidine-2-ones N-alkylpyrrolidines Benzene and substituted derivatives Tertiary carboxylic acid amides 1,3-dioxoles Oxacyclic compounds Acetals Dialkyl ethers Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Plicamine alkaloid skeleton - Alpha-amino acid or derivatives - Azaspirodecane - Indole or derivatives - Piperidinone - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Delta-lactam - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Monocyclic benzene moiety - Piperidine - Benzenoid - Pyrrolidine - Tertiary carboxylic acid amide - Meta-dioxole - Lactam - Carboxamide group - Acetal - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen 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