Compound Identification
SMILES
CNC1CC(OC)C=CC11C(=O)N(CCC2=CC=CC=C2)C(=O)C2=CC3=C(OCO3)C=C12
InChIKey
InChIKey=WJRGXPFJBXWWPF-UHFFFAOYSA-N
Formula
C25H26N2O5
Mass
434.492
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Amaryllidaceae alkaloids
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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
1,3-isoquinolinediones Isoquinolones and derivatives Tetrahydroisoquinolines Azaspirodecane derivatives Benzodioxoles Piperidinediones Delta lactams N-substituted carboxylic acid imides N-acyl amines Benzene and substituted derivatives Dicarboximides 1,3-dioxoles Amino acids and derivatives Oxacyclic compounds Dialkylamines Dialkyl ethers Azacyclic compounds Acetals Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Plicamine alkaloid skeleton - 1,3-isoquinolinedione - Isoquinolone - Tetrahydroisoquinoline - Azaspirodecane - Benzodioxole - Piperidinedione - Piperidinone - Delta-lactam - Benzenoid - Piperidine - Carboxylic acid imide, n-substituted - N-acyl-amine - Monocyclic benzene moiety - Dicarboximide - Carboxylic acid imide - Meta-dioxole - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Ether - Secondary aliphatic amine - Dialkyl ether - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - 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