Compound Identification
SMILES
COC1CC2N(C)CC3N(CCCC(O)=O)C(=O)C4=CC5=C(OCO5)C=C4C23C=C1
InChIKey
InChIKey=NQLAFBGWNJKINY-UHFFFAOYSA-N
Formula
C22H26N2O6
Mass
414.458
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 Tetrahydroisoquinolines Azaspirodecane derivatives Indoles and derivatives Benzodioxoles Piperidinones Delta lactams N-alkylpyrrolidines N-acyl amines Benzenoids Tertiary carboxylic acid amides 1,3-dioxoles Trialkylamines Amino acids Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Azacyclic compounds Acetals Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Plicamine alkaloid skeleton - Isoquinolone - Tetrahydroisoquinoline - Azaspirodecane - Indole or derivatives - Benzodioxole - Piperidinone - Delta-lactam - Benzenoid - N-alkylpyrrolidine - Piperidine - N-acyl-amine - Tertiary carboxylic acid amide - Pyrrolidine - Meta-dioxole - Amino acid - Tertiary aliphatic amine - Tertiary amine - Lactam - Carboxamide group - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - 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