Compound Identification
SMILES
COC1=C(OC)C=C2C(=C1)N([C@H]1C[C@@H]3CCN(C)CC[C@]21C(=O)\C3=C\C)C(C)=O
InChIKey
InChIKey=SSEGBBKFPCLCKO-MMHPIKLDSA-N
Formula
C23H30N2O4
Mass
398.503
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Condylocarpan alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Condylocarpan alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Condylocarpan alkaloids
Alternative Parents
Carbazoles Anisoles Aralkylamines Alkyl aryl ethers Tertiary carboxylic acid amides Acetamides Trialkylamines Ketones Amino acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Condylocarpan skeleton - Carbazole - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Aralkylamine - Benzenoid - Tertiary carboxylic acid amide - Acetamide - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxamide group - Ketone - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as condylocarpan alkaloids. These are alkaloids with a structure based on the condylocarpan backbone. These alkaloids contain a ring system similar to that of the curan group, but are formed by cyclisation of C-21 on to C-7 in a Corynanthe precursor, rather than the formation of a 3,7 bond.
External Descriptors
Not available