The Administrative Core serves a critical function for the Program Project, serving as the administrative arm and central focal point for organization and dissemination of scientific, budgetary, and other information which are associated with the Program Project. It also will coordinate all communication among the different groups that are involved in the Program Project. Manuscript preparations, slide presentations, etc. involving the Principal Investigator, correspondence, purchasing of supplies and services, arrangements for PPG meetings, photocopying and dissemination of information and presentations, purchasing of supplies and other things necessary for research, preparation and records of traveling to scientific meetings by the Program Project group, oversite of financial matters, maintenance and upkeep of data bases, and other administrative functions as needed will be coordinated by the Administrative Core. All correspondence, arrangements for outside scientific visitors related to the Program Project, coordination of activities with outside collaborators, and other related administrative functions will be coordinated by the Core. Finally, the Administrative Core provides the focal point for the extensive local collaborative efforts and cooperations which have marked the success of the Program Project in the past and into the future.
There are still many unmet public health needs in the treatment of pain and drug abuse in our society and worldwide. In this research we will examine the design, synthesis, and biological evaluation of novel peptide and peptidomimetic ligands for the treatment of prolonged pain, especially neuropathic pain that will address new mechanism of pain control with minimal side effects, drug seeking behavior and tolerance.
|Bannister, Kirsty; Qu, Chaoling; Navratilova, Edita et al. (2017) Multiple sites and actions of gabapentin-induced relief of ongoing experimental neuropathic pain. Pain 158:2386-2395|
|Vardanyan, Ruben S; Cain, James P; Haghighi, Saghar Mowlazadeh et al. (2017) Synthesis and Investigation of Mixed ?-Opioid and ?-Opioid Agonists as Possible Bivalent Ligands for Treatment of Pain. J Heterocycl Chem 54:1228-1235|
|Sandweiss, A J; McIntosh, M I; Moutal, A et al. (2017) Genetic and pharmacological antagonism of NK1 receptor prevents opiate abuse potential. Mol Psychiatry :|
|Cai, Minying; Marelli, Udaya Kiran; Mertz, Blake et al. (2017) Structural Insights into Selective Ligand-Receptor Interactions Leading to Receptor Inactivation Utilizing Selective Melanocortin 3 Receptor Antagonists. Biochemistry 56:4201-4209|
|Hall, Sara M; LeBaron, Lindsay; Ramos-Colon, Cyf et al. (2016) Discovery of Stable Non-opioid Dynorphin A Analogues Interacting at the Bradykinin Receptors for the Treatment of Neuropathic Pain. ACS Chem Neurosci 7:1746-1752|
|Deekonda, Srinivas; Rankin, David; Davis, Peg et al. (2016) Design synthesis and structure-activity relationship of 5-substituted (tetrahydronaphthalen-2yl)methyl with N-phenyl-N-(piperidin-2-yl)propionamide derivatives as opioid ligands. Bioorg Med Chem 24:85-91|
|Lee, Yeon Sun; Remesic, Michael; Ramos-Colon, Cyf et al. (2016) Cyclic non-opioid dynorphin A analogues for the bradykinin receptors. Bioorg Med Chem Lett 26:5513-5516|
|Remesic, Michael; Lee, Yeon Sun; Hruby, Victor J (2016) Cyclic Opioid Peptides. Curr Med Chem 23:1288-303|
|Ramos-Colon, Cyf N; Lee, Yeon Sun; Remesic, Michael et al. (2016) Structure-Activity Relationships of [des-Arg7]Dynorphin A Analogues at the ? Opioid Receptor. J Med Chem 59:10291-10298|
|Deekonda, Srinivas; Cole, Jacob; Sunna, Sydney et al. (2016) Enkephalin analogues with N-phenyl-N-(piperidin-2-ylmethyl)propionamide derivatives: Synthesis and biological evaluations. Bioorg Med Chem Lett 26:222-7|
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