Compound Identification
SMILES
CS[C@@]12C[C@@]34[C@H](N(COC[C@]5(SC)N(C)C(=O)[C@@](CC6=CN3C3=CC=CC=C63)(SC)N(C)C5=O)C3=CC=CC=C43)N1C(=O)[C@@](CO)(SC)N(C)C2=O
InChIKey
InChIKey=DOTYKRRRMXXIPL-BSTWCIEHSA-N
Formula
C36H42N6O6S4
Mass
783.01
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
Pyrroloindoles Alpha amino acids and derivatives 3-alkylindoles Thiodioxopiperazines Dialkylarylamines N-methylpiperazines Benzenoids Tertiary carboxylic acid amides Pyrrolidines Pyrroles Heteroaromatic compounds Lactams Thiohemiaminal derivatives Sulfenyl compounds Oxacyclic compounds Dialkylthioethers Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Pyrroloindole - 3-alkylindole - Alpha-amino acid or derivatives - Thiodioxopiperazine - Indole or derivatives - Indole - Dialkylarylamine - 2,5-dioxopiperazine - Dioxopiperazine - N-alkylpiperazine - N-methylpiperazine - Benzenoid - Piperazine - 1,4-diazinane - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrolidine - Pyrrole - Lactam - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Sulfenyl compound - Hemithioaminal - Thioether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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