Compound Identification
SMILES
CC[C@@H]1[C@H](O)[C@@H](C)OCC\C(C)=C/C[C@H](NC(=O)C[C@H](O)C(C)(C)C1=O)C(\F)=C\C1=CC=CC=N1
InChIKey
InChIKey=LIZPTPQKGNXERE-YFYOQUPZSA-N
Formula
C27H39FN2O5
Mass
490.616
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Macrolactams
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Macrolactams
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Macrolactams
Alternative Parents
Pyridines and derivatives Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Vinyl fluorides Oxacyclic compounds Fluoroalkenes Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Macrolactam - Pyridine - Heteroaromatic compound - Carboxamide group - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Organoheterocyclic compound - Dialkyl ether - Vinyl halide - Vinyl fluoride - Carboxylic acid derivative - Oxacycle - Azacycle - Fluoroalkene - Haloalkene - Ether - Hydrocarbon derivative - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Alcohol - Organic oxide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.
External Descriptors
Not available