Compound Identification
SMILES
COC(=O)[C@@H]1[C@@H]2C[C@@H]3N(CC[C@@]45C6=CC7=C(C=C6O[C@@]34N1C1=CC=CC=C51)[C@@]13CCN4C\C(=C\C)[C@@H](C[C@H]4[C@@H]1N7C)[C@H]3C(=O)OC)C\C2=C\C
InChIKey
InChIKey=DQCQZSHDSKTQMX-LQAAYDTDSA-N
Formula
C41H46N4O5
Mass
674.842
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 Carbazoles Quinolizidines Naphthyridines Coumarans Piperidinecarboxylic acids Dialkylarylamines Aralkylamines Dicarboxylic acids and derivatives Benzenoids Methyl esters Trialkylamines Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pleiocarpaman skeleton - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Carbazole - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - Quinolizidine - Coumaran - Indole or derivatives - Piperidinecarboxylic acid - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Aralkylamine - Benzenoid - Piperidine - Dicarboxylic acid or derivatives - Methyl ester - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organic oxygen 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