Structure Information
Structure

Compound Identification

SMILES

OC(CCCCC(O)=N[C@@H]1C[C@@H]2N(C1)C(=O)C1=NC(=CC=C1)N=C(O)[C@@H]1CCCN1C(=O)C1=NC(=CC=C1)N=C(O)[C@@H]1CCCN1C(=O)C1=NC(=CC=C1)N=C2O)=N[C@@H]1C[C@@H]2N(C1)C(=O)C1=NC(=CC=C1)N=C(O)[C@@H]1CCCN1C(=O)C1=NC(=CC=C1)N=C(O)[C@@H]1CCCN1C(=O)C1=NC(=CC=C1)N=C2O

InChIKey

InChIKey=HAAMYECPKFPNJA-WJERRADFSA-N

Formula

C72H74N20O14

Mass

1443.51

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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 - 2-heteroaryl carboxamide - Pyridine - Pyrrolidine - Tertiary carboxylic acid amide - Cyclic carboximidic acid - Heteroaromatic compound - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carboximidic acid derivative - Polyol - Carboximidic acid - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen 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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