Lisa Wilson
Affiliations: | 2017-2022 | Pharmacodynamics | University of Florida |
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Wilson LL, Alleyne AR, Eans SO, et al. (2022) Characterization of CM-398, a Novel Selective Sigma-2 Receptor Ligand, as a Potential Therapeutic for Neuropathic Pain. Molecules (Basel, Switzerland). 27 |
Wilson LL, Eans SO, Ramadan-Siraj I, et al. (2022) Examination of the Novel Sigma-1 Receptor Antagonist, SI 1/28, for Antinociceptive and Anti-allodynic Efficacy against Multiple Types of Nociception with Fewer Liabilities of Use. International Journal of Molecular Sciences. 23 |
Chakraborty S, Uprety R, Slocum ST, et al. (2021) Oxidative Metabolism as a Modulator of Kratom's Biological Actions. Journal of Medicinal Chemistry |
Chakraborty S, DiBerto JF, Faouzi A, et al. (2021) A Novel Mitragynine Analog with Low-Efficacy Mu Opioid Receptor Agonism Displays Antinociception with Attenuated Adverse Effects. Journal of Medicinal Chemistry |
Romeo G, Bonanno F, Wilson LL, et al. (2021) Development of New Benzylpiperazine Derivatives as σ Receptor Ligands with Antinociceptive and Anti-Allodynic Effects. Acs Chemical Neuroscience |
Wilson LL, Chakraborty S, Eans SO, et al. (2021) Kratom Alkaloids, Natural and Semi-Synthetic, Show Less Physical Dependence and Ameliorate Opioid Withdrawal. Cellular and Molecular Neurobiology |
Wilson LL, Harris HM, Eans SO, et al. (2020) Lyophilized Kratom Tea as a Therapeutic Option for Opioid Dependence. Drug and Alcohol Dependence. 216: 108310 |
Intagliata S, Sharma A, King TI, et al. (2020) Discovery of a Highly Selective Sigma-2 Receptor Ligand, 1-(4-(6,7-Dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)butyl)-3-methyl-1H-benzo[d]imidazol-2(3H)-one (CM398), with Drug-Like Properties and Antinociceptive Effects In Vivo. The Aaps Journal. 22: 94 |
Brice-Tutt AC, Wilson LL, Eans SO, et al. (2020) Multifunctional Opioid Receptor Agonism and Antagonism by a Novel Macrocyclic Tetrapeptide Prevents Reinstatement of Morphine-Seeking Behavior. British Journal of Pharmacology |
Ferracane MJ, Brice-Tutt A, Coleman J, et al. (2020) Design, Synthesis, and Characterization of the Macrocyclic Tetrapeptide [Pro-Sar-Phe-D-Phe]: a Mixed Opioid Receptor Agonist-Antagonist Following Oral Administration. Acs Chemical Neuroscience |