Structure Information
Structure

Compound Identification

SMILES

CC[C@H](C)[C@@H]1NC(=O)[C@H](CC2=CC=C(O)C=C2)N(C)C(=O)[C@H]([C@@H](C)CC)N2[C@H](O)CC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]3[C@@H](OC1=O)C(C)CN3C(=O)[C@H](CCC(N)=O)NC(=O)CC)C2=O

InChIKey

InChIKey=GRVMTANYFFVRTL-FXWCSWMSSA-N

Formula

C47H72N8O12

Mass

941.137

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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 heteropolycyclic compounds

Substituents

Cyclic depsipeptide - Macrolide lactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid ester - Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-acylpyrrolidine - Delta-lactam - 1-hydroxy-2-unsubstituted benzenoid - Piperidinone - Phenol - Fatty acyl - Benzenoid - Fatty amide - Piperidine - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Pyrrolidine - Lactam - Primary carboxylic acid amide - Secondary carboxylic acid amide - Lactone - Carboxylic acid ester - Carboxamide group - Alkanolamine - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Aromatic 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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