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Articles

Peer-Reviewed Papers

N ε-Acryloyllysine Piperazides as Irreversible Inhibitors of Transglutaminase 2: Synthesis, Structure?Activity Relationships, and Pharmacokinetic Profiling.Wodtke R, et al. Journal of Medicinal Chemistry, 61(10), 4528-4560 (2018) Polymethacrylates containing a 4-amino-pyridyl derivative covalently attached as effective catalysts in acylation chemistry: self-activation by neighboring group effectsMennenga T, et al. Polymer International, 64(12), 1685-1689 (2015) Benzimidazo [2, 1-a] benz [de] isoquinoline-7-one-12-carboxylic acid based fluorescent sensors for pH and Fe3+Zhao Y, et al. Journal of Photochemistry and Photobiology A: Chemistry, 314(12), 52-59 (2016) Synthesis, characterization, and bioactivity of new bisamidrazone derivatives as possible anticancer agents.Al-Qtaitat M A, et al. Medicinal Chemistry Research, 27(5), 1419-1431 (2018) Identification and biological evaluation of 4-(3-trifluoromethylpyridin-2-yl) piperazine-1-carboxylic acid (5-trifluoromethylpyridin-2-yl) amide, a high affinity TRPV1 (VR1) vanilloid receptor antagonist.Swanson D M, et al. Journal of Medicinal Chemistry, 48(6), 1857-1872 (2005) Identification of ML204: a novel potent antagonist that selectively modulates native TRPC4/C5 channels.Miller M, et al. The Journal of Biological Chemistry, jbc-M111 (2011) Synthesis and biological activity of novel tert-butyl and tert-pentylphenoxyalkyl piperazine derivatives as histamine H3R ligands.Szczepanska K, et al. European Journal of Medicinal Chemistry, 152, 223-234 (2018) Selenium dioxide-mediated synthesis of ?-ketoamides from arylglyoxals and secondary aminesShaw AY, et al. Tetrahedron Letters, 53(32), 4151-4153 (2012) Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibioticsNaidu BN, et al. Bioorganic & Medicinal Chemistry, 14(22), 5573-5577 (2004) Synthesis and biological activity of novel tert-butyl and tert-pentylphenoxyalkyl piperazine derivatives as histamine H3R ligandsSzczepanska K, et al. European Journal of Medicinal Chemistry, 152(12), 223-234 (2018)

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