Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C[C@@H](C)\C=C(C)\C[C@H](C)C(=O)N[C@@H](CO)C(=O)N(C)[C@H](CC2=CC(I)=C(O)C=C2)C(=O)N[C@@H](C)C(=O)O1

InChIKey

InChIKey=OZGGBCWQMMSVKW-NRVAOJETSA-N

Formula

C28H40IN3O7

Mass

657.546

Export to:

JSON SDF CSV

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 - 2-iodophenol - 2-halophenol - 1-hydroxy-2-unsubstituted benzenoid - Iodobenzene - Phenol - Halobenzene - Benzenoid - Aryl iodide - Aryl halide - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Lactam - Lactone - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organohalogen compound - Organic nitrogen compound - Organoiodide - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Primary alcohol - 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

Previous Back Next