Vadim S. Korotkov
Braunschweig, NI, Germany
Last Updated: 09/26/2026
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Found 22 publications
An Imidazo[2,1-b][1,3,4]thiadiazole Derivative Inhibits the Virulence Factor α-Hemolysin by Blocking the Pullout of Its Stem Domain.
Journal: ChemMedChem
Published: December 08, 2025
Discovery of synthetic small molecules targeting the central regulator of Salmonella pathogenicity.
Journal: Science advances
Published: April 11, 2025
Highly potent quinoxalinediones inhibit α-hemolysin and ameliorate Staphylococcus aureus lung infections.
Journal: Cell host & microbe
Published: August 23, 2024
Hydantoin analogs inhibit the fully assembled ClpXP protease without affecting the individual peptidase and chaperone domains.
Journal: Organic & biomolecular chemistry
Published: July 18, 2019
Repurposing human kinase inhibitors to create an antibiotic active against drug-resistant Staphylococcus aureus, persisters and biofilms.
Journal: Nature chemistry
Published: May 10, 2019
Neocarzilin A Is a Potent Inhibitor of Cancer Cell Motility Targeting VAT-1 Controlled Pathways.
Journal: ACS central science
Published: March 15, 2019
Design and synthesis of tailored human caseinolytic protease P inhibitors.
Journal: Chemical communications (Cambridge, England)
Published: August 16, 2018
Selective Activation of Human Caseinolytic Protease P (ClpP).
Journal: Angewandte Chemie (International ed. in English)
Published: July 17, 2018
A Chemical Disruptor of the ClpX Chaperone Complex Attenuates the Virulence of Multidrug-Resistant Staphylococcus aureus.
Journal: Angewandte Chemie (International ed. in English)
Published: August 16, 2017
A chemical compound inhibiting the Aha1-Hsp90 chaperone complex.
Journal: The Journal of biological chemistry
Published: May 19, 2017
Last Updated: 09/26/2026