Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(NCCCCCCCCOC3=C(C)C4=C(C=C3)C(=O)C=C(O4)N3CCOCC3)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O
InChIKey
InChIKey=RLASFQOSINVYEP-BLCDGAFUSA-N
Formula
C50H68N4O12
Mass
917.11
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
Chromones Phenol ethers Dialkylarylamines Pyranones and derivatives Alkyl aryl ethers Morpholines Vinylogous amides Carbamate esters Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Oxacyclic compounds Azacyclic compounds Dialkylamines Dialkyl ethers Enamines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Chromone - Benzopyran - 1-benzopyran - Phenol ether - Dialkylarylamine - Alkyl aryl ether - Pyranone - Morpholine - Oxazinane - Pyran - Benzenoid - Vinylogous amide - Carbamic acid ester - Heteroaromatic compound - Amino acid or derivatives - Cyclic ketone - Carboxamide group - Ketone - Lactam - Tertiary amine - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Azacycle - Ether - Enamine - Secondary aliphatic amine - Dialkyl ether - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - 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