Compound Identification
SMILES
COC1CC2N(C)C(=O)C3N(CCC4=CC=C(O)C=C4)C(=O)C4=CC5=C(OCO5)C(O)C4(O)C23C=C1
InChIKey
InChIKey=QGBUVEMSRZZGST-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
Azaspirodecane derivatives Alpha amino acids and derivatives Indoles and derivatives Delta lactams 1-hydroxy-2-unsubstituted benzenoids Piperidinones N-alkylpyrrolidines Benzene and substituted derivatives Pyrrolidine-2-ones 1,3-dioxoles Tertiary carboxylic acid amides Tertiary alcohols 1,2-diols Secondary alcohols Acetals Dialkyl ethers Azacyclic compounds Oxacyclic 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 - 1-hydroxy-2-unsubstituted benzenoid - Delta-lactam - Phenol - Piperidinone - Monocyclic benzene moiety - Piperidine - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Meta-dioxole - Tertiary carboxylic acid amide - Tertiary alcohol - Secondary alcohol - Lactam - 1,2-diol - Carboxamide group - Azacycle - Acetal - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Alcohol - Organopnictogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - 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