Jessica P. Anand, Ph.D.
Affiliations: | Medicinal Chemistry | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Opiod signal transductions, addictionGoogle:
"Jessica Anand"Mean distance: 21373.2
Parents
Sign in to add mentor| John R. Traynor | grad student | 2013 | University of Michigan | |
| (The Mu and Delta Opioid Receptors: Mixed Efficacy Ligands and Receptor Trafficking.) | ||||
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Publications
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| Disney A, Olson KM, Shafer AM, et al. (2022) Opioid Antagonists from the Orvinol Series as Potential Reversal Agents for Opioid Overdose. Acs Chemical Neuroscience |
| Henry S, Anand JP, Brinkel AC, et al. (2020) SAR Matrices Enable Discovery of Mixed Efficacy μ-Opioid Receptor Agonist Peptidomimetics with Simplified Structures through an Aromatic-Amine Pharmacophore. Acs Chemical Neuroscience |
| Hassanien SH, Bassman JR, Perrien Naccarato CM, et al. (2020) In vitro Pharmacology of Fentanyl Analogs at the Human Mu Opioid Receptor and Their Spectroscopic Analysis. Drug Testing and Analysis |
| Henry S, Anand JP, Twarozynski JJ, et al. (2020) Aromatic-Amine Pendants Produce Highly Potent and Efficacious Mixed Efficacy Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetics with Enhanced Metabolic Stability. Journal of Medicinal Chemistry |
| Montgomery D, Anand JP, Baber MA, et al. (2019) Structure-Activity Relationships of 7-Substituted Dimethyltyrosine-Tetrahydroisoquinoline Opioid Peptidomimetics. Molecules (Basel, Switzerland). 24 |
| Montgomery D, Anand JP, Griggs N, et al. (2019) Novel Dimethyltyrosine-Tetrahydroisoquinoline Peptidomimetics with Aromatic Tetrahydroisoquinoline Substitutions Show In Vitro Kappa and Mu Opioid Receptor Agonism. Acs Chemical Neuroscience |
| Henry S, Fernandez TM, Anand JP, et al. (2019) Structural Simplification of a Tetrahydroquinoline Core Peptidomimetic µ-Opioid-Receptor (MOR) Agonist/ δ-Opioid Receptor (DOR) Antagonist Produces Improved Metabolic Stability . Journal of Medicinal Chemistry |
| Nastase AF, Anand JP, Bender AM, et al. (2019) Dual Pharmacophores Explored via Structure-Activity Relationship (SAR) Matrix: Insights into Potent, Bifunctional Opioid Ligand Design. Journal of Medicinal Chemistry |
| Nastase AF, Griggs NW, Anand JP, et al. (2018) Synthesis and pharmacological evaluation of novel C-8 substituted tetrahydroquinolines as balanced-affinity mu/delta opioid ligands for the treatment of pain. Acs Chemical Neuroscience |
| Anand JP, Montgomery D. (2018) Multifunctional Opioid Ligands. Handbook of Experimental Pharmacology |