Compound Identification
SMILES
CC[C@@]12CCC[N+]3([O-])CCC4=C([C@H]13)N([C@@H](C2)OC)C1=CC=CC=C41
InChIKey
InChIKey=KFAHAKAGWDLBIH-VIXCBWPKSA-N
Formula
C20H26N2O2
Mass
326.44
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 Beta carbolines 3-alkylindoles Naphthyridines Benzenoids Piperidines Trialkyl amine oxides Pyrroles Heteroaromatic compounds Trisubstituted amine oxides and derivatives Azacyclic compounds Organooxygen compounds Hydrocarbon derivatives Organic salts Organic oxides Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Piperidine - Benzenoid - Heteroaromatic compound - Pyrrole - Trialkyl amine oxide - Trisubstituted n-oxide - N-oxide - Organoheterocyclic compound - Azacycle - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organic salt - Organic cation - 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