Compound Identification
SMILES
COC1=CC2=CC(=NC(O[C@@H]3C[C@@H]4N(C3)C(=O)N(C)CCCC\C=C/[C@@H]3C[C@@]3(NC4=O)C(O)=O)=C2C=C1)C1=CSC(NC(C)C)=N1
InChIKey
InChIKey=HSPPJWFPANDCCK-COMIVOALSA-N
Formula
C33H40N6O6S
Mass
648.78
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
Alpha amino acids and derivatives Isoquinolines and derivatives Anisoles 2,4-disubstituted thiazoles Alkyl aryl ethers 2-amino-1,3-thiazoles Pyridines and derivatives Cyclopropanecarboxylic acids Pyrrolidines Heteroaromatic compounds Lactams Ureas Secondary carboxylic acid amides Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Carbonyl compounds Amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid or derivatives - Isoquinoline - Anisole - Phenol ether - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - 1,3-thiazol-2-amine - Cyclopropanecarboxylic acid - Benzenoid - Cyclopropanecarboxylic acid or derivatives - Pyridine - Heteroaromatic compound - Azole - Thiazole - Pyrrolidine - Carboxamide group - Urea - Secondary carboxylic acid amide - Lactam - Ether - Organoheterocyclic compound - Carboxylic acid - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Amine - Organooxygen compound - Organonitrogen 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