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Page 1
Synthesis and Pharmacological Evaluation of Enantiomerically Pure GluN2B Selective NMDA Receptor Antagonists.
ChemMedChem. 2018 Aug 10;13(15):1580-1587. doi: 10.1002/cmdc.201800214. Epub 2018 Jul 4.
ChemMedChem. 2018.
PMID: 29806151
Fluorinated GluN2B Receptor Antagonists with a 3-Benzazepine Scaffold Designed for PET Studies.
Szermerski M, Börgel F, Schepmann D, Haider A, Betzel T, Ametamey SM, Wünsch B.
Szermerski M, et al.
ChemMedChem. 2018 May 23;13(10):1058-1068. doi: 10.1002/cmdc.201700819. Epub 2018 Apr 17.
ChemMedChem. 2018.
PMID: 29522653
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Synthesis, biological evaluation and molecular docking studies of benzyloxyacetohydroxamic acids as LpxC inhibitors.
Szermerski M, Melesina J, Wichapong K, Löppenberg M, Jose J, Sippl W, Holl R.
Szermerski M, et al.
Bioorg Med Chem. 2014 Feb 1;22(3):1016-28. doi: 10.1016/j.bmc.2013.12.057. Epub 2014 Jan 3.
Bioorg Med Chem. 2014.
PMID: 24412340
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Evaluation of 11C-Me-NB1 as a Potential PET Radioligand for Measuring GluN2B-Containing NMDA Receptors, Drug Occupancy, and Receptor Cross Talk.
Krämer SD, Betzel T, Mu L, Haider A, Herde AM, Boninsegni AK, Keller C, Szermerski M, Schibli R, Wünsch B, Ametamey SM.
Krämer SD, et al. Among authors: szermerski m.
J Nucl Med. 2018 Apr;59(4):698-703. doi: 10.2967/jnumed.117.200451. Epub 2017 Nov 30.
J Nucl Med. 2018.
PMID: 29191857
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