Structure Information
Structure

Compound Identification

SMILES

COC1C=COC2(C)OC3=C(C)C(OC(=O)C4=CC=C(C)C=C4)=C4C(=O)C(NC(=O)C(C)=CC=CC(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)=C(N1CCCCC1)C(=O)C4=C3C2=O

InChIKey

InChIKey=XVVOKYPBUCCTSF-UHFFFAOYSA-N

Formula

C50H60N2O13

Mass

897.031

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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 - Naphthoquinone - Benzoate ester - Naphthalene - Benzofuran - Benzoic acid or derivatives - Coumaran - Benzoyl - Quinone - Aryl ketone - Aryl alkyl ketone - Toluene - Ketal - Benzenoid - Piperidine - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Vinylogous amide - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid ester - Amino acid or derivatives - Ketone - Lactam - Acetal - Ether - Enamine - Oxacycle - Dialkyl ether - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Amine - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen 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

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