Compound Identification
SMILES
CC[C@H](NC1=C(NSN1)\N=C1/C=CC=C(C(=O)N2CCC[C@@H](O)C2)C1=O)C1=CC(=CO1)C(C)C
InChIKey
InChIKey=NZZIKQVIPJZIRM-IEOJPGKSSA-N
Formula
C24H31N5O4S
Mass
485.6
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
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Class
Piperidines
- Subclass N-acylpiperidines
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Class
Piperidines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Piperidines
Subclass
N-acylpiperidines
Intermediate Tree Nodes
Not available
Direct Parent
N-acylpiperidines
Alternative Parents
O-quinonimines Tertiary carboxylic acid amides Secondary ketimines Heteroaromatic compounds Furans Azomethines Secondary alcohols Cyclic ketones Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N-acyl-piperidine - O-quinonimine - Quinonimine - Azomethine - Furan - Heteroaromatic compound - Tertiary carboxylic acid amide - Secondary ketimine - Carboxamide group - Ketimine - Ketone - Secondary alcohol - Cyclic ketone - Carboxylic acid derivative - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Imine - Organopnictogen compound - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as n-acylpiperidines. These are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of a piperidine.
External Descriptors
Not available