Compound Identification
SMILES
COC1=C2OC3=C(OC)C=CC(=C3)C(=O)O[C@H]3C=COC=C4[C@@H](O)[C@@]56SS[C@@]([C@@H](O)C(C=C1)=C2)(N(C)C5=O)C(=O)N6[C@H]34
InChIKey
InChIKey=BPRXOIXJSLNVCK-KCEIGVIJSA-N
Formula
C28H24N2O10S2
Mass
612.62
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
Diarylethers Alpha amino acids and derivatives Epipolythiodioxopiperazines Anisoles Alkyl aryl ethers N-methylpiperazines Dithiazinanes Tertiary carboxylic acid amides Pyrrolidines Secondary alcohols Carboxylic acid esters Organic disulfides Lactones Lactams Oxacyclic compounds Organic oxides Organonitrogen compounds Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Diaryl ether - Alpha-amino acid or derivatives - Epipolythiodioxopiperazine - Thiodioxopiperazine - Anisole - Dioxopiperazine - Phenol ether - 2,5-dioxopiperazine - Alkyl aryl ether - N-alkylpiperazine - N-methylpiperazine - Dithiazinane - 1,4-diazinane - Piperazine - Benzenoid - Tertiary carboxylic acid amide - Pyrrolidine - Secondary alcohol - Organic disulfide - Lactone - Lactam - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Ether - Oxacycle - Carboxylic acid derivative - Organic oxide - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - 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