Compound Identification
SMILES
CC1C2[C@H](CC3=CNC4=CC=CC=C34)NC(=O)[C@@]22[C@@H](\C=C\C[C@H](C)CC(=O)[C@@H]3O[C@H]3C2=O)[C@@H]2O[C@]12C
InChIKey
InChIKey=ZZBBNMBXFLZWMG-TUGDVINLSA-N
Formula
C29H32N2O5
Mass
488.584
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Cytochalasans
- Subclass Chaetoglobosins
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Class
Cytochalasans
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Cytochalasans
Subclass
Chaetoglobosins
Intermediate Tree Nodes
Not available
Direct Parent
Chaetoglobosins
Alternative Parents
3-alkylindoles Isoindolones Oxepanes Substituted pyrroles Pyrrolidine-2-ones Benzenoids Heteroaromatic compounds Secondary carboxylic acid amides Lactams Ketones Oxacyclic compounds Azacyclic compounds Dialkyl ethers Epoxides Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Carbocyclic chaetoglobosin skeleton - Isoindolone - 3-alkylindole - Indole - Indole or derivatives - Isoindoline - Isoindole or derivatives - Oxepane - Benzenoid - Substituted pyrrole - 2-pyrrolidone - Pyrrolidone - Heteroaromatic compound - Pyrrole - Pyrrolidine - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Oxirane - Dialkyl ether - Azacycle - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as chaetoglobosins. These are cytochalasans with a structure in which the hydrogenated isoindole bears an (indol-3-yl)methyl group.
External Descriptors
Not available