Compound Identification
SMILES
CC(C)(C)OC(=O)N[C@@H](CC1=CNC2=CC=CC=C12)C(=O)NNC(=O)SC1CCN(C1=O)C1=CC=CC=C1
InChIKey
InChIKey=QWOMUCNWJXFRMD-HMTLIYDFSA-N
Formula
C27H31N5O5S
Mass
537.64
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Indoles and derivatives
- Subclass Tryptamines and derivatives
-
Class
Indoles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Indoles and derivatives
Subclass
Tryptamines and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Tryptamines and derivatives
Alternative Parents
Phenylpyrrolidines 3-alkylindoles Alpha amino acids and derivatives Benzene and substituted derivatives Substituted pyrroles Pyrrolidine-2-ones Tertiary carboxylic acid amides Carbamate esters Heteroaromatic compounds Carboxylic acid hydrazides Tertiary amines Lactams Azacyclic compounds Sulfenyl compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Triptan - 1-phenylpyrrolidine - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Monocyclic benzene moiety - Pyrrolidone - 2-pyrrolidone - Substituted pyrrole - Benzenoid - Tertiary carboxylic acid amide - Pyrrole - Heteroaromatic compound - Carbamic acid ester - Pyrrolidine - Tertiary amine - Lactam - Amino acid or derivatives - Carboxylic acid hydrazide - Carboxamide group - Azacycle - Carboxylic acid derivative - Sulfenyl compound - Amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as tryptamines and derivatives. These are compounds containing the tryptamine backbone, which is structurally characterized by an indole ring substituted at the 3-position by an ethanamine.
External Descriptors
Not available