Compound Identification
SMILES
CC[C@]12C[C@@H](N3C4=CC=CC=C4C4=C3[C@H]1N(CC4)CC=C2)C1=CC2=C(N[C@]34[C@H](C)[C@@]5(C[C@H]3C(=O)OC)C=CCN3CC[C@]24[C@H]53)C=C1
InChIKey
InChIKey=NTCLEOOXPJPREQ-FVNDCLGZSA-N
Formula
C40H44N4O2
Mass
612.818
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 Carbazoles 2,3-Cyclopentanoindolines 3-alkylindoles Naphthyridines Aromatic monoterpenoids Secondary alkylarylamines Aralkylamines N-alkylpyrrolidines Benzenoids Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Amino acids and derivatives Azacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - 2,3-cyclopentanoindoline - Aromatic monoterpenoid - Monoterpenoid - Norbornane monoterpenoid - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Methyl ester - Pyrrolidine - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Secondary amine - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organic oxygen 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