Compound Identification
SMILES
[H]\C(C)=C1\C(=O)[C@@]23CCN(C)CC[C@]1([H])C[C@@]2([H])N(C(C)=O)C1=C3C=CC(OC)=C1O
InChIKey
InChIKey=HXWIJPIEAIUMKA-ZHEWFFLKSA-N
Formula
C22H28N2O4
Mass
384.476
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 1-hydroxy-4-unsubstituted benzenoids Tertiary carboxylic acid amides Acetamides Trialkylamines Ketones Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Condylocarpan skeleton - Carbazole - Indole or derivatives - Anisole - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Aralkylamine - Benzenoid - Tertiary carboxylic acid amide - Acetamide - Amino acid or derivatives - Carboxamide group - Ketone - Tertiary amine - Tertiary aliphatic amine - Ether - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Amine - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - 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