Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C2=O)C2=C(C(O)=C3C)C(O)=C(NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)C(\C=N\N1CCN(CC1)C1CCCC1)=C2O

InChIKey

InChIKey=WDZCUPBHRAEYDL-GZAUEHORSA-N

Formula

C47H64N4O12

Mass

877.045

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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 - Naphthofuran - 1-naphthol - Naphthalene - Benzofuran - Coumaran - Hydroquinone - Aryl ketone - Aryl alkyl ketone - Ketal - N-alkylpiperazine - 1,4-diazinane - Piperazine - Benzenoid - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Polyol - Oxacycle - Azacycle - Dialkyl ether - Acetal - Ether - Hydrazone - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - 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

CHEBI:45304 : N-alkylpiperazine - N-iminopiperazine - rifamycin

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