Compound Identification
SMILES
COC1=CC2=CC(N(C)C(=O)CC(O)C3(C)OC3C(C)C3CC(O)(NC(=O)O3)C(C)\C=C\C=C(C)\C2)=C1Cl
InChIKey
InChIKey=VULREKHOQTWFEH-KZVYIGENSA-N
Formula
C28H37ClN2O7
Mass
549.06
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
Anisoles Alkyl aryl ethers 1,3-oxazinanes Aryl chlorides Tertiary carboxylic acid amides Carbamate esters Secondary alcohols Lactams Oxacyclic compounds Alkanolamines Azacyclic compounds Epoxides Dialkyl ethers Organochlorides Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Anisole - Phenol ether - Alkyl aryl ether - 1,3-oxazinane - Aryl halide - Benzenoid - Oxazinane - Aryl chloride - Carbamic acid ester - Tertiary carboxylic acid amide - Lactam - Carboxamide group - Secondary alcohol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Alkanolamine - Ether - Oxirane - Dialkyl ether - Organic nitrogen compound - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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