Docking and structure activity relationship studies of potent and selective thiazolidinethione GSK-3 inhibitors
Glycogen synthase kinase-3 (GSK-3) plays a key role in several biochemical pathways and is an attractive target for pharmacological intervention. We prepared a series of analogs of a highly selective thiazolidinethione inhibitor of GSK-3. The structure-activity relationship indicated a precise structural requirement for potent inhibition. We used docking and bioinformatic analysis to explore the rationale for the potency and selectivity of this class of GSK-3 inhibitors. These computational studies identified residues unique to GSK-3 likely to play a role in ligand-specific induced fit interactions. Together, these studies highlight the structural stringency of specific kinase inhibition that can be achieved for GSK-3.
Authors
- Crina M. Orac
- Davoud Ghazanfari
- Stephen C. Bergmeier (ORCID: https://orcid.org/0000-0003-3891-8442)
- Hannah Boesger (ORCID: https://orcid.org/0000-0002-5634-369X)
- Emily A. Fairchild (ORCID: https://orcid.org/0000-0002-0226-6801)
- Mahboubeh S. Noori
- Douglas J. Goetz (ORCID: https://orcid.org/0000-0003-3666-5373)
- Keith Williams (ORCID: https://orcid.org/0000-0003-2581-0491)
- Jennifer V. Hines (ORCID: https://orcid.org/0000-0001-9812-3137)
- Jon Pritchard
- Opeyemi O Fatunbi
- Sa Adatu Abdullai
- Brianna Hubble
- Deborah K Amesaki
Institutions
- Ohio University (US)
Publication Details
- Journal
- Bioorganic & Medicinal Chemistry Letters
- Published
- 2024-12-16
- DOI
- https://doi.org/10.1016/j.bmcl.2024.130074
- Citations
- 1
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.36
Funders
- National Science Foundation
- National Institutes of Health