Compound Identification
SMILES
OC[C@H]1OCCN2C=C(C3=CC=CC=C23)C2=C(C(=O)NC2=O)C2=CN(C[C@@H]1F)C1=CC=CC=C21
InChIKey
InChIKey=APVNUYSTGPZNSJ-SIKLNZKXSA-N
Formula
C26H22FN3O4
Mass
459.477
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
Indoles Maleimides Benzenoids Pyrrolines Pyrroles Dicarboximides Heteroaromatic compounds N-unsubstituted carboxylic acid imides Azacyclic compounds Dialkyl ethers Oxacyclic compounds Organonitrogen compounds Primary alcohols Alkyl fluorides Carbonyl compounds Hydrocarbon derivatives Organofluorides Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Indole - Indole or derivatives - Maleimide - Benzenoid - Carboxylic acid imide - Dicarboximide - Heteroaromatic compound - Carboxylic acid imide, n-unsubstituted - Pyrrole - Pyrroline - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Alkyl halide - Organic oxygen compound - Alkyl fluoride - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Alcohol - Aromatic heteropolycyclic 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