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Chemmedchem|April 9, 2019
Optimization of Drug Candidates That Inhibit the D-Loop Activity of RAD51Brian Budke, Werner Tueckmantel, Kelsey Miles, et al.
ACS Medicinal Chemistry Letters|May 20, 2017
Design and Synthesis of Mercaptoacetamides as Potent, Selective, and Brain Permeable Histone Deacetylase 6 InhibitorsWei Lv, Guangming Zhang, Cyril Barinka, et al.
Bioorganic & Medicinal Chemistry Letters|May 8, 2009
Isoxazole moiety in the linker region of HDAC inhibitors adjacent to the Zn-chelating group: effects on HDAC biology and antiproliferative activitySubhasish Tapadar, Rong He, Doris N Luchini, et al.
Organic & Biomolecular Chemistry|December 11, 2003
Functionalization of the alicyclic skeleton of epibatidine: synthesis and nicotinic acetylcholine receptor binding affinities of epibatidine analoguesZhi-Liang Wei, Yingxian Xiao, Clifford George, et al.
Current Topics in Medicinal Chemistry|January 31, 2012
Derivatives of 3-isoxazolecarboxylic acid esters: a potent and selective compound class against replicating and nonreplicating Mycobacterium tuberculosisAnnamaria Lilienkampf, Marco Pieroni, Scott G Franzblau, et al.
ACS Medicinal Chemistry Letters|November 16, 2018
2-Aminoadipic Acid-C(O)-Glutamate Based Prostate-Specific Membrane Antigen Ligands for Potential Use as TheranosticsRyo Nakajima, Zora Nováková, Werner Tueckmantel, et al.
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