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Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@@H]1[C@H](O)[C@H](C)[C@H](O)[C@H](C)C=CC=C(C)C(=O)NC2=C(C)C(OC(C)=O)=C3C(=C(O)C(C)=C4OCOC(=C34)C(C)=C[C@@](C)(O)[C@H](O)[C@@H](C)[C@H]1OC(C)=O)C2=O

InChIKey

InChIKey=OFTBCJGFYRLYFS-QROZXHQHSA-N

Formula

C42H53NO15

Mass

811.878

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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 - Benzo-m-dioxin - Tricarboxylic acid or derivatives - Aryl ketone - Beta-hydroxy acid - Hydroxy acid - Benzenoid - Enol ester - Tertiary alcohol - Methyl ester - Vinylogous acid - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Carboxylic acid derivative - Acetal - Polyol - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Alcohol - Organic oxygen compound - Carbonyl group - 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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