Compound Identification
SMILES
C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)NC(=O)C22[C@@H](\C=C\C[C@H](C)CC(=O)CCC2=O)[C@@H]2O[C@]12C
InChIKey
InChIKey=YGKUXRWMCOUTAL-VQXBHXPGSA-N
Formula
C29H34N2O4
Mass
474.601
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 Cyclic ketones Lactams 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 - Pyrrolidone - 2-pyrrolidone - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrolidine - Pyrrole - Carboxamide group - Secondary carboxylic acid amide - Cyclic ketone - Ketone - Lactam - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Dialkyl ether - Oxirane - Ether - Oxacycle - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organonitrogen 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