Compound Identification
SMILES
COC(=O)[C@@H]1[C@H]2C[C@@H]3N(CC[C@@]45CC6=C(O[C@@]34N1C1=CC=CC=C51)C(=O)C=CO6)C\C2=C\C
InChIKey
InChIKey=RINWKYUPYDFBMH-BCWJYCDBSA-N
Formula
C26H26N2O5
Mass
446.503
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Pleiocarpaman alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Pleiocarpaman alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pleiocarpaman alkaloids
Alternative Parents
Indolonaphthyridine alkaloids Alpha amino acid esters Beta carbolines Naphthyridines Quinolizidines Piperidinecarboxylic acids Dialkylarylamines Aralkylamines Pyranones and derivatives Benzenoids Methyl esters Heteroaromatic compounds Trialkylamines Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pleiocarpaman skeleton - 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 - Pyranone - Benzenoid - Piperidine - Pyran - Methyl ester - Heteroaromatic compound - Carboxylic acid ester - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organonitrogen compound - Amine - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pleiocarpaman alkaloids. These are alkaloids with a structure that is based on the pleiocarpaman skeleton. These alkaloids arise from the cyclization of a corynantheine precursor via C-16 to N-1.
External Descriptors
Not available