Compound Identification
SMILES
CO[C@@H](C[C@H](C)CC1=C(NCCCCNC2=C3C[C@@H](C)C[C@H](OC)[C@H](O)[C@@H](C)\C=C(C)/[C@H](OC(N)=O)[C@@H](OC)\C=C/C=C(C)\C(=O)NC(=CC2=O)C3=O)C(=O)C=C(N)C1=O)[C@H](O)[C@@H](C)\C=C(/C)[C@H](OC(N)=O)[C@@H](OC)\C=C\C=C(/C)C(=O)OC
InChIKey
InChIKey=BNOIPNWUMZYVLH-LLTYHFODSA-N
Formula
C61H88N6O17
Mass
1177.4
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
P-benzoquinones Fatty acid esters Vinylogous amides Carbamate esters Enoate esters Methyl esters Secondary carboxylic acid amides Secondary alcohols Lactams Azacyclic compounds Dialkyl ethers Dialkylamines Monocarboxylic acids and derivatives Enamines Organic oxides Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - P-benzoquinone - Quinone - Fatty acid ester - Fatty acyl - Carbamic acid ester - Methyl ester - Vinylogous amide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Cyclic ketone - Lactam - Ketone - Secondary carboxylic acid amide - Carboxylic acid ester - Secondary alcohol - Carboxamide group - Amino acid or derivatives - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Azacycle - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Carbonyl group - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Organic oxide - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Primary amine - Aliphatic 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