Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCC1CC(=O)N2CCCC2C(=O)NC(CO)C(=O)N2CCCC2C(=O)NC(CCCN=C(N)N)C(=O)NC(C(O)C(O)=O)C(=O)NC(CO)C(=O)N2CCC(O)C2C(=O)NC(C(O)C(O)=O)C(=O)O1

InChIKey

InChIKey=WSCOCOSDPASNLN-UHFFFAOYSA-N

Formula

C49H79N11O19

Mass

1126.229

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Depsipeptides

Intermediate Tree Nodes

Not available

Direct Parent

Cyclic depsipeptides

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - Alpha-amino acid ester - Macrolide - Macrolactam - Alpha-amino acid or derivatives - Tricarboxylic acid or derivatives - Alpha-hydroxy acid - Hydroxy acid - Pyrrolidine - Tertiary carboxylic acid amide - Lactone - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Guanidine - Carboxylic acid ester - Carboxamide group - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

External Descriptors

Not available

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