Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1C[C@H](C)CC2=C(NCC3CCN(CC3)C(=O)C3=NC=NC=C3C(O)=O)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O

InChIKey

InChIKey=SNVSBMOUDBUNCS-QUSJEVESSA-N

Formula

C40H52N6O11

Mass

792.887

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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 - N-acyl-piperidine - Pyrimidine-5-carboxylic acid - Pyrimidine-5-carboxylic acid or derivatives - Pyrimidine-6-carboxylic acid or derivatives - 2-heteroaryl carboxamide - Piperidine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Tertiary carboxylic acid amide - Carbamic acid ester - Amino acid or derivatives - Carboxamide group - Ketone - Lactam - Amino acid - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Carboxylic acid - Carboxylic acid derivative - Secondary amine - Organoheterocyclic compound - Azacycle - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Hydrocarbon derivative - Carbonyl group - Amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - 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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