Structure Information
Structure

Compound Identification

SMILES

CNC(=O)CC1NC(=O)C2=CSC(=N2)C2=C(N=C(C=C2)C2=NC(=CS2)C(=O)OCC2NC(=O)C3CCCN3C2=O)C2=CSC(=N2)C2=CSC(=N2)C(NC(=O)CNC(=O)C2=CSC(=N2)C(NC(=O)C2=C(C)SC1=N2)C(C)C)C(C)C

InChIKey

InChIKey=RVTQSVRTXQTCKX-UHFFFAOYSA-N

Formula

C50H50N14O9S6

Mass

1183.4

Export to:

JSON SDF CSV

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 - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Dioxopiperazine - 2-heteroaryl carboxamide - 2,5-dioxopiperazine - Thiazolecarboxylic acid or derivatives - N-alkylpiperazine - 2,4-disubstituted 1,3-thiazole - Pyridine - 1,4-diazinane - Piperazine - Azole - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Organopnictogen 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

Previous Back Next