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Synthesis and late stage modifications of Cyl derivatives.

ABSTRACT: A peptide Claisen rearrangement is used as key step to generate a tetrapeptide with a C-terminal double unsaturated side chain. Activation and cyclization give direct access to cyclopeptides related to naturally occurring histone deacetylase (HDAC) inhibitors Cyl-1 and Cyl-2. Late stage modifications on the unsaturated amino acid side chain allow the introduction of functionalities which might coordinate to metal ions in the active center of metalloproteins, such as histone deacetylases.

SUBMITTER: Servatius P

PROVIDER: S-EPMC8822456 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

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Synthesis and late stage modifications of Cyl derivatives.

Servatius Phil P Kazmaier Uli U

Beilstein journal of organic chemistry 20220204

A peptide Claisen rearrangement is used as key step to generate a tetrapeptide with a C-terminal double unsaturated side chain. Activation and cyclization give direct access to cyclopeptides related to naturally occurring histone deacetylase (HDAC) inhibitors Cyl-1 and Cyl-2. Late stage modifications on the unsaturated amino acid side chain allow the introduction of functionalities which might coordinate to metal ions in the active center of metalloproteins, such as histone deacetylases. ...[more]

PMID: 35186154

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