Structure Information
Structure

Compound Identification

SMILES

CC(C)[C@H](O)C(=O)N[C@H]1CC2=CC3=C(OC4OC5=C6C=CC=C5[C@@]34C3=C(N=C(O3)[C@@H](NC1=O)C(C)C)C1=NC(Cl)=C(O1)C1=C(Cl)NC3=CC=CC6=C13)C=C2

InChIKey

InChIKey=VPDPIMFYGMSFGQ-LJVQVHOFSA-N

Formula

C40H33Cl2N5O7

Mass

766.63

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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

N-acyl-alpha amino acid or derivatives - Macrolactam - Alpha-amino acid or derivatives - Coumaran - Indole - Indole or derivatives - Aryl chloride - Aryl halide - N-acyl-amine - Fatty amide - Fatty acyl - Benzenoid - Substituted pyrrole - Azole - Heteroaromatic compound - Oxazole - Pyrrole - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen 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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