Ann M. Decker

Synthesis and biological evaluation of bupropion analogues as potential pharmacotherapies for cocaine addiction.

H. Navarro, F. Carroll, B. Blough, 2009, Journal of medicinal chemistry.

Potent and Selective Tetrahydroisoquinoline Kappa Opioid Receptor Antagonists of Lead Compound (3 R)-7-Hydroxy- N-[(1 S)-2-methyl-1-(piperidin-1-ylmethyl)propyl]-1,2,3,4-tetrahydroisoquinoline-3-carboxamide (PDTic).

T. Fennell, R. Snyder, James B. Thomas, 2018, Journal of medicinal chemistry.

Potent and Selective Tetrahydroisoquinoline Kappa Opioid Receptor Antagonists of Lead Compound (3 R)- N-[1 R)-1-(Cyclohexylmethyl)-2-methylpropyl]-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxamide (CDTic).

T. Fennell, R. Snyder, James B. Thomas, 2018, Journal of medicinal chemistry.

Design, synthesis, and pharmacological evaluation of JDTic analogs to examine the significance of replacement of the 3-hydroxyphenyl group with pyridine or thiophene bioisosteres.

James B. Thomas, S. Runyon, C. Kormos, 2016, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of bupropion analogues as potential pharmacotherapies for smoking cessation.

R. Lukas, S. Mascarella, H. Navarro, 2009, Journal of medicinal chemistry.