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Replacement of the Benzylpiperidine Moiety with Fluorinated Phenylalkyl Side Chains for the Development of GluN2B Receptor Ligands.
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- ChemMedChem, 2018, v. 13, n. 23, p. 2522, doi. 10.1002/cmdc.201800566
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Molecular structure of a brominated 2-benzazepinone - a crucial intermediate in the synthesis of novel chemokine CCR2 receptor antagonists.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2017, v. 72, n. 6, p. 421, doi. 10.1515/znb-2017-0030
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- Article
Synthesis and pharmacological evaluation of fluorinated benzo[7]annulen‐7‐amines as GluN2B‐selective NMDA receptor antagonists.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2019, v. 62, n. 8, p. 354, doi. 10.1002/jlcr.3718
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A common mechanism allows selective targeting of GluN2B subunit-containing N-methyl-D-aspartate receptors.
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- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0645-6
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