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Chemmedchem|June 22, 2018
Tertiary-Amine-Based Inhibitors of the Astacin Protease Meprin αKathrin Tan, Christian Jäger, Dagmar Schlenzig, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|January 20, 2023
Synthesis and structure-activity relationships of pyrazole-based inhibitors of meprin α and βKathrin Tan, Christian Jäger, Stefanie Geissler, et al.
Journal of Medicinal Chemistry|December 23, 2025
Crosstalk between NLRP3 Signaling and Histone Deacetylases in Inflammasome-Driven DiseasesKathrin Tan, M Mercedes Rodríguez-Fernández, Tim Keuler, et al.
ACS Medicinal Chemistry Letters|July 14, 2026
Targeting Histone Acetyltransferases EP300/CBP by Novel Proline-Based PROTAC DegradersKathrin Tan, Melina Vogt, Katerina Schaal, et al.
European Journal of Medicinal Chemistry|November 16, 2024
Multicomponent syntheses enable the discovery of novel quisinostat-derived chemotypes as histone deacetylase inhibitorsDaniel Stopper, Susanna Buntrock, Kathrin Tan, et al.
ACS Pharmacology & Translational Science|September 19, 2025
Target Engagement Studies and Kinetic Live-Cell Degradation Assays Enable the Systematic Characterization of Histone Deacetylase 6 DegradersMaria Hanl, Felix Feller, Irina Honin, et al.
European Journal of Medicinal Chemistry|May 7, 2024
Preferential HDAC6 inhibitors derived from HPOB exhibit synergistic antileukemia activity in combination with decitabineMaik Tretbar, Julian Schliehe-Diecks, Lukas von Bredow, et al.
ACS Pharmacology & Translational Science|March 20, 2025
Contilisant-Belinostat Hybrids: Polyfunctionalized Indole Derivatives as Multineurotarget Drugs for the Potential Treatment of Alzheimer's DiseaseLinda Schäker-Hübner, Mireia Toledano-Pinedo, Sophia Eimermacher, et al.
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