Structure Information
Structure

Compound Identification

SMILES

CCC(O)(CC)C(=O)N[C@H]1CC2=CC3=C(OC4NC5=C6C=CC=C5C34C3=C(N=C(O3)[C@@H](NC1=O)C(C)C)C1=NC=C(O1)C1=CNC3=C(OP(O)(O)=O)C=CC6=C13)C=C2

InChIKey

InChIKey=HCSIGLASGYFOSQ-TYKOKSJISA-N

Formula

C41H39N6O10P

Mass

806.769

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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-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Aryl phosphate - Aryl phosphomonoester - Indole - Coumaran - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Fatty amide - N-acyl-amine - Fatty acyl - Benzenoid - Organic phosphoric acid derivative - Phosphoric acid ester - Azole - Heteroaromatic compound - Tertiary alcohol - Oxazole - Pyrrole - Secondary carboxylic acid amide - Lactam - Amino acid or derivatives - Carboxamide group - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organonitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Organooxygen compound - Organic nitrogen compound - Amine - 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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