Compound Identification
SMILES
CC[C@@]12CCCN3CCC4=C([C@H]13)N([C@H](C2)C1=CC2=C(N[C@]35[C@H](C)[C@@]6(C[C@H]3C(=O)OC)C=CCN3CC[C@]25[C@H]63)C=C1)C1=CC=CC=C41
InChIKey
InChIKey=MZITZBZTMCXZQS-FVNDCLGZSA-N
Formula
C40H46N4O2
Mass
614.834
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 Aromatic monoterpenoids Naphthyridines 3-alkylindoles Secondary alkylarylamines Aralkylamines Piperidines Benzenoids N-alkylpyrrolidines Heteroaromatic compounds Pyrroles Methyl esters Amino acids and derivatives Trialkylamines Monocarboxylic acids and derivatives Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - 2,3-cyclopentanoindoline - Aromatic monoterpenoid - Norbornane monoterpenoid - Monoterpenoid - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Dihydroindole - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyrrolidine - Pyrrole - Methyl ester - Heteroaromatic compound - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Secondary amine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Organooxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen 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