Structure Information
Structure

Compound Identification

SMILES

COC1C=COC2(C)OC3=C(C2=O)C2=C(C(O)=C3C)C(=O)C(NC(=O)C(C)=CC=CC(=C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)=C1NC3(CCN(CC(C)C)CC3)N=C21

InChIKey

InChIKey=DYBBMCQDCATCGZ-UHFFFAOYSA-N

Formula

C46H60N4O11

Mass

845.003

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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

Naphthofuran - Macrolactam - Azaspirodecane - Naphthalene - Benzofuran - Coumaran - Aryl ketone - Aryl alkyl ketone - Ketal - Piperidine - Benzenoid - 3-imidazoline - Vinylogous amide - Vinylogous acid - Lactam - Ketimine - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxylic acid ester - Ketone - Carboxamide group - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Polyol - Secondary amine - Organic oxygen compound - Organopnictogen compound - Imine - Carbonyl group - Organic oxide - Alcohol - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - 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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