Compound Identification
SMILES
CCC12CCCN(C1)c1nc3cc(O)c(cc3c(C=C)c1C2)C1CC2(CC)CCCN3CCc4c(C23)n1c1ccccc41
InChIKey
InChIKey=ZEWZJFWYVWSQKO-UHFFFAOYSA-N
Formula
C38H44N4O
Mass
572.797
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 Aminoquinolines and derivatives 3-alkylindoles Naphthyridines Dialkylarylamines 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Pyridines and derivatives Piperidines Imidolactams Pyrroles Heteroaromatic compounds Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organooxygen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Pyridoindole - Beta-carboline - Aminoquinoline - Diazanaphthalene - Quinoline - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Dialkylarylamine - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Imidolactam - Pyridine - Benzenoid - Piperidine - Heteroaromatic compound - Pyrrole - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organonitrogen 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