Compound Identification
SMILES
CC1C2C(CC3=CNC4=CC=CC=C34)NC(=O)C22C(\C=C\CC(C)CC(O)C(O)CC2=O)C2OC12C
InChIKey
InChIKey=LECKOZQNFFNOND-RMKNXTFCSA-N
Formula
C29H36N2O5
Mass
492.616
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 Secondary alcohols 1,2-diols 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 - Pyrrolidone - 2-pyrrolidone - Heteroaromatic compound - Pyrrole - Pyrrolidine - Carboxamide group - Ketone - Lactam - 1,2-diol - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Ether - Oxirane - Dialkyl ether - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - 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