Compound Identification
SMILES
CCC12CCCN3CCC4C(C13)N(C1=CC=CC=C41)C(O)(C2)C(=O)OC
InChIKey
InChIKey=ZOYUWDAPINYCFF-UHFFFAOYSA-N
Formula
C21H28N2O3
Mass
356.466
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Eburnan-type alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Eburnan-type alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Eburnan-type alkaloids
Alternative Parents
Indolonaphthyridine alkaloids Alpha amino acid esters Beta carbolines Quinolizidines Naphthyridines Piperidinecarboxylic acids Dialkylarylamines Aralkylamines Benzenoids Methyl esters Trialkylamines Monocarboxylic acids and derivatives Alkanolamines Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - Quinolizidine - Indole or derivatives - Piperidinecarboxylic acid - Dialkylarylamine - Aralkylamine - Piperidine - Benzenoid - Methyl ester - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Alkanolamine - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organonitrogen compound - Amine - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.
External Descriptors
Not available