Synthesis of paramagnetic ligands that target the C-terminal binding site of Hsp90.
Bioorg Med Chem Lett
; 30(16): 127303, 2020 08 15.
Article
em En
| MEDLINE
| ID: mdl-32631523
Identification of a ligand binding site represents the starting point for a structure-based drug development program. Lack of a binding site hampers the development of improved ligands that modulate the protein of interest. In this letter, we describe the development of chemical tools that will allow for elucidation of the Hsp90 C-terminal ligand binding site. Our strategy is based on the preparation of paramagnetic analogs of KU-596, an investigational new drug that is currently undergoing clinical trials for the treatment of neuropathy and interacts with the Hsp90 C-terminal domain. In particular, we report the design and synthesis of three novel paramagnetic analogs of KU-596, which will be used to obtain long range distances for NMR structural studies of Hsp90 in complex with C-terminal ligands.
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Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Fenetilaminas
/
Proteínas de Choque Térmico HSP90
/
Glicosídeos
Limite:
Humans
Idioma:
En
Revista:
Bioorg Med Chem Lett
Assunto da revista:
BIOQUIMICA
/
QUIMICA
Ano de publicação:
2020
Tipo de documento:
Article