Structure Information
Structure

Compound Identification

SMILES

CC\C=C1\NC(=O)\C=C\[C@@H](OC(=O)C(C)(C)[C@H](C[C@@H](OC)\C=C\C=C\C\C=C/CCC(C)C)OC(=O)CNC(=O)[C@H](CNC(N)=O)NC(=O)CNC(=O)[C@@H](CCCNC(=O)NS(O)(=O)=O)NC1=O)C(C)C

InChIKey

InChIKey=BWYSWRDMLZWXES-GWIODXKASA-N

Formula

C46H73N9O15S

Mass

1024.2

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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 heteromonocyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - N-acyl-alpha amino acid or derivatives - Macrolactam - Alpha-amino acid ester - Alpha-amino acid amide - Beta amino acid or derivatives - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - Fatty acid ester - Fatty acyl - N-acyl-amine - Fatty amide - Dicarboxylic acid or derivatives - Organic sulfuric acid or derivatives - Carbonic acid derivative - Lactone - Lactam - Carboxylic acid ester - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic 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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