Compound Identification
SMILES
ONC(=O)[C@@H](CC1=CNC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(Br)C=C1
InChIKey
InChIKey=IKIYSDPJUPLPFZ-MRXNPFEDSA-N
Formula
C17H16BrN3O4S
Mass
438.3
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
3-alkylindoles Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Bromobenzenes Substituted pyrroles Organosulfonamides Aryl bromides Aminosulfonyl compounds Heteroaromatic compounds Hydroxamic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organobromides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Triptan - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - 3-alkylindole - Benzenesulfonamide - Benzenesulfonyl group - Indole - Halobenzene - Bromobenzene - Aryl bromide - Aryl halide - Benzenoid - Organosulfonic acid amide - Monocyclic benzene moiety - Substituted pyrrole - Heteroaromatic compound - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - Pyrrole - Organosulfonic acid or derivatives - Hydroxamic acid - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organohalogen compound - Organobromide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen 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 subsituted at the 3-position by an ethanamine.
External Descriptors
Not available