Compound Identification
SMILES
CO[C@H]1\C=C\O[C@@]2(C)CC3=C(C)C(O)=C4C(O)=C(NC(=O)\C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](O)[C@@H]1C)\C(=C/NN1CCN(C)CC1)C(=O)C4=C3C2=O
InChIKey
InChIKey=QSIOUFWLAOSBLS-BOTZVGGNSA-N
Formula
C42H58N4O10
Mass
778.944
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
Indanones Naphthols and derivatives Aryl alkyl ketones O-quinomethanes N-methylpiperazines Phenols Vinylogous amides Secondary alcohols Secondary carboxylic acid amides Lactams Trialkylamines Amino acids and derivatives Oxacyclic compounds Alkylhydrazines Dialkyl ethers Azacyclic compounds Polyols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Indanone - 1-naphthol - Naphthalene - Indane - O-quinomethane - Quinomethane - Aryl alkyl ketone - Aryl ketone - Phenol - N-methylpiperazine - N-alkylpiperazine - 1,4-diazinane - Piperazine - Benzenoid - Vinylogous amide - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Carboxamide group - Ketone - Lactam - Organoheterocyclic compound - Polyol - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Alkylhydrazine - Oxacycle - Hydrazine derivative - Amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - 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