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Structure Information
Structure

Compound Identification

SMILES

CC=C(NC(=O)C1=CSC(=N1)C1=CSC(=N1)C1=NC2=C(C=C1)C1=NC(=CS1)C(=O)NC(C(C)O)C(=O)NC(=CC)C1=NC(=CS1)C(=O)NC(C1=NC(=CS1)C(=O)NC(C(C)O)C1=NC2=CS1)C(C)(C)O)C(=O)NCC(C)O

InChIKey

InChIKey=FEORQDDAQBRWPT-UHFFFAOYSA-N

Formula

C48H49N13O10S6

Mass

1160.36

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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 amide - Alpha-amino acid or derivatives - 2-heteroaryl carboxamide - Thiazolecarboxylic acid or derivatives - Thiazolecarboxamide - 2,4-disubstituted 1,3-thiazole - N-acyl-amine - Pyridine - Azole - Heteroaromatic compound - Thiazole - Tertiary alcohol - Carboxamide group - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - 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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