Compound Identification
SMILES
CCC(C)CN1C2C(=O)N(C)C3CC(OC)C=CC23C2=CC3=C(OCO3)C=C2C1=O
InChIKey
InChIKey=XUBQMUBIMYIJLL-UHFFFAOYSA-N
Formula
C23H28N2O5
Mass
412.486
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 Alpha amino acids and derivatives Piperidinecarboxamides Indoles and derivatives Benzodioxoles Piperidinones Delta lactams Pyrrolidine-2-ones N-alkylpyrrolidines N-acyl amines Benzenoids Tertiary carboxylic acid amides 1,3-dioxoles Oxacyclic compounds Dialkyl ethers Azacyclic compounds Acetals Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Plicamine alkaloid skeleton - Isoquinolone - Tetrahydroisoquinoline - Azaspirodecane - Alpha-amino acid or derivatives - Piperidinecarboxamide - 2-piperidinecarboxamide - Indole or derivatives - Benzodioxole - Piperidinone - Delta-lactam - Benzenoid - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Piperidine - N-acyl-amine - Tertiary carboxylic acid amide - Pyrrolidine - Meta-dioxole - Lactam - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen 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