Structure Information
Structure

Compound Identification

SMILES

C[C@H]1[C@@H](O)CN2[C@H]1C1=NC(=CS1)C1=NC(=CS1)C1=C(C=CC(=N1)C1=NC(=CS1)C(=O)N1CCNCC1)C1=NC(=CS1)C(=O)N[C@@H](CC(N)=O)C1=NC(=C(C)S1)C(=O)N[C@@H]([C@H](O)C1=CC=CC=C1)C1=NC(=CS1)C(=O)N[C@@H](CC1=CC=C(OC(=O)NCCN3CCOCC3)C=C1)C2=O

InChIKey

InChIKey=SOXZMPRJMWSYHN-GWQCVFHDSA-N

Formula

C64H64N16O11S6

Mass

1425.68

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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 - Beta amino acid or derivatives - Alpha-amino acid or derivatives - 2-heteroaryl carboxamide - Phenoxy compound - Thiazolecarboxamide - Thiazolecarboxylic acid or derivatives - 2,4-disubstituted 1,3-thiazole - Morpholine - Oxazinane - Monocyclic benzene moiety - Piperazine - Benzenoid - 1,4-diazinane - Pyridine - Azole - Heteroaromatic compound - Carbamic acid ester - Pyrrolidine - Tertiary carboxylic acid amide - Thiazole - Secondary alcohol - Carboxamide group - Lactam - Secondary carboxylic acid amide - Tertiary amine - Primary carboxylic acid amide - Tertiary aliphatic amine - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Secondary amine - Organic oxygen compound - Carbonyl group - Alcohol - Amine - Organic oxide - Aromatic alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen 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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