Structure Information
Structure

Compound Identification

SMILES

COC1C=COC2(C)Oc3c(C2=O)c2c(cc(NC(=O)C(C)=CC=CC(C)(O)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)c(O)c2c(O)c3C)N1CCCC1C(C)O

InChIKey

InChIKey=ZFQIISWIJYKBBY-UHFFFAOYSA-N

Formula

C43H58N2O13

Mass

810.938

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolactams

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolactams

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macrolactam - Naphthofuran - 1-naphthol - Naphthalene - Benzofuran - Coumaran - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Aryl alkyl ketone - Aryl ketone - Ketal - Benzenoid - Pyrrolidine - Tertiary alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Monocarboxylic acid or derivatives - Polyol - Carboxylic acid derivative - Acetal - Ether - Dialkyl ether - Alcohol - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - 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

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