Structure Information
Structure

Compound Identification

SMILES

[H]C1=C(C)C(=O)OC([H])(C(O)=NC([H])(C)C(=O)N(C)C([H])(CC2=CC=CC=C2)C(=O)N(C)CC(O)=NC([H])(C(=O)N(C)C([H])(C)C(=O)OC([H])(C([H])(C)CC)C([H])(C)C([H])(O)C1)C([H])(C)CC)C([H])(C)CC

InChIKey

InChIKey=VOJKUGWTQYFABB-UHFFFAOYSA-N

Formula

C45H71N5O10

Mass

842.088

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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

Aromatic heteromonocyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - Alpha-amino acid ester - Macrolide - Macrolactam - Alpha-amino acid or derivatives - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Tertiary carboxylic acid amide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Cyclic carboximidic acid - Carboxylic acid ester - Secondary alcohol - Lactam - Carboxamide group - Lactone - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic 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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