Compound Identification
SMILES
COC(=O)C1[C@H]2C[C@@H]3N(CC[C@@]45OC(=O)N[C@@]34N1C1=CC=CC=C51)C\C2=C\C
InChIKey
InChIKey=MRMLDAGRWKCMNW-OCRMKOIDSA-N
Formula
C21H23N3O4
Mass
381.432
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 Quinolizidines Azaspirodecane derivatives Naphthyridines Piperidinecarboxylic acids Dialkylarylamines Aralkylamines Oxazolidinones Benzenoids Methyl esters Carbamate esters Trialkylamines Monocarboxylic acids and derivatives Oxacyclic compounds Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives
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 - Azaspirodecane - Naphthyridine - Quinolizidine - Indole or derivatives - Piperidinecarboxylic acid - Dialkylarylamine - Aralkylamine - Oxazolidinone - Piperidine - Benzenoid - Methyl ester - Carbamic acid ester - Oxazolidine - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organic nitrogen compound - Organonitrogen 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