Structure Information
Structure

Compound Identification

SMILES

CCC(C)N1CCC2(CC1)NC1=C3NC(=O)\C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)C(O)[C@@H](C)[C@H](O)[C@H](C)[C@@H](OC)\C=C\O[C@@]4(C)OC5=C(C)C(O)=C(C3=O)C(C1=N2)=C5C4=O

InChIKey

InChIKey=DEOYQVBCXCVHII-GSNHDGFMSA-N

Formula

C44H60N4O10

Mass

804.982

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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 - Ketone - Ketimine - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Lactam - Carboxamide group - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Enamine - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Amine - Aldehyde - Organic nitrogen compound - Hydrocarbon derivative - Imine - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Alcohol - 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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