Thomas Edward Prisinzano

School of Pharmacy - Medicinal Chemistry
Professor
Chair, Medicinal Chemistry
Primary office:
785-864-3267
Malott Hall
Room 4070
The University of Kansas
1251 Wescoe Hall Dr.
Lawrence, KS 66045-7582
Second office:



Thomas E. Prisinzano earned a B.S. in chemistry from the University of Delaware, Newark, DE in 1995 and a PhD in Medicinal Chemistry from Virginia Commonwealth University, Richmond, VA in 2000. He teaches graduate courses, Medicinal Chemistry I, and Undergraduate Research. He has received the Matt Suffness (Young Investigator) Award from the American Society of Pharmacognosy (2008), Joseph Cochin Young Investigator Award from the College on Problems of Drug Dependence (2011), and the David W. Robertson Award for Excellence in Medicinal Chemistry from the American Chemical Society (2012). His research combines natural product isolation and medicinal chemistry and is focused on identification of novel agonists and antagonists at CNS receptors from natural sources. In particular, he has focused on understanding the chemistry and pharmacology associated with Salvia divinorum, a hallucinogenic mint plant native to Oaxaca, Mexico.

Research Interests

  • Opioid
  • Analgesics
  • Drugs of abuse
  • Drug discovery
  • CNS

Selected Publications

Jamshidi, R. J, Jacobs, B. A, Sullivan, L. C, Chavera, T. A, Saylor, R. M, Prisinzano, T. E, Clarke, W. P, & Berg, K. A (2015). Functional Selectivity of Kappa Opioid Receptor Agonists in Peripheral Sensory Neurons. The Journal of pharmacology and experimental therapeutics, 355(2), 174-82. DOI:10.1124/jpet.115.225896

Riley, A. P, Groer, C. E, Young, D., Ewald, A. W, Kivell, B. M, & Prisinzano, T. E (2014). Synthesis and κ-Opioid Receptor Activity of Furan-Substituted Salvinorin A Analogues. Journal of medicinal chemistry, 57(24), 10464-75. DOI:10.1021/jm501521d

Kivell, B. M, Ewald, A. W, & Prisinzano, T. E (2014). Salvinorin A analogs and other kappa-opioid receptor compounds as treatments for cocaine abuse. In L. P Dwoskin (Ed.), Emerging Targets and Therapeutics for the Treatment of Psychostimulant Drug Abuse (Vol. 69, pp. 481-511). DOI:10.1016/B978-0-12-420118-7.00012-3

Prisinzano, T. E. (2013). 2012 David W. Robertson Award Address: Neoclerodanes as Atypical Opioid Receptor Ligands. J. Med. Chem., 56, 3435-3543.

Riley, A. P., Day, V. W., Navarro, H. A., & Prisinzano, T. E. (2013). Palladium-Catalyzed Transformations of Salvinorin A, a Neoclerodane Diterpene from Salvia divinorum. Org. Lett., 15, 5936-5939. DOI:10.1021/ol4027528

Vasiljevik, T., Franks, L. N., Ford, B. M., Douglas, J. T., Prather, P. L., Fantegrossi, W. E., & Prisinzano, T. E. (2013). Design, synthesis, and biological evaluation of aminoalkylindole derivatives as cannabinoid receptor ligands with potential for treatment of alcohol abuse. J. Med. Chem., 56(11), 4537–4550. DOI:10.1021/jm400268b

MacLean, K. A., Johnson, M. W., Reissig, C. J., Prisinzano, T. E., & Griffiths, R. R. (2013). Dose-related effects of salvinorin A in humans: dissociative, hallucinogenic, and memory effects. Psychopharmacology (Berl.), 226(2), 381–392. DOI:10.1007/s00213-012-2912-9

Selected Grants

Bohn, L. M., (Principal), Aubé, J., (Principal), Prisinzano, T. E., (Consultant), Novel Probes of the Kappa Opioid Receptor: Chemistry, Pharmacology, and Biology, R01 DA031927-01, National Institutes of Health, $495,487, (06/01/2011 - 04/30/2016) . Federal. Status: Funded.

Prisinzano, T. E., (Principal), Investigation of Neoclerodanes as Novel Opioid Ligands, 5R01DA018151-06, National Institutes of Health, $270,275, (09/01/2010 - 08/31/2015) . Federal. Status: Funded.

Hanson, P. R., (Co-Principal), Prisinzano, T. E., (Co-Principal), Training Grant in Dynamic Aspects of Chemical Biology, 2T32GM008545-17, National Institutes of Health, $394,533, (07/01/2010 - 06/30/2015) . Federal. Status: Funded.


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