T. Capiris

发表

(Aryloxy)alkylamines as selective human dopamine D4 receptor antagonists: potential antipsychotic agents.

T. Heffner, R. Doubleday, D. T. Connor, 1997, Journal of medicinal chemistry.

The preparation of optically active α-amino 4H-[1,2,4]oxadiazol-5-ones from optically active α-amino acids

T. Belliotti, M. Stier, Matthew R. Johnson, 2009 .

Structure-activity relationships of pregabalin and analogues that target the alpha(2)-delta protein.

T. Heffner, A. Thorpe, L. Wise, 2005, Journal of medicinal chemistry.

Pyrazolo[1,5-a]pyrimidine CRF-1 receptor antagonists.

T. Heffner, H. Akunne, R. Mackenzie, 1998, Bioorganic & medicinal chemistry letters.

The demethylation of 1,2,3,4,5,6,7,8-octahydro-1-(2-methoxybenzyl)-2-methylisoquinoline. The synthesis of 1-hydroxy-N-methylmorphinan and 1,2,3,4,4a,5,6,7,7a,8-deeahydro-7-methyl[1]benzopyrano[2,3-j]isoquinoline

T. Capiris, S. Lazarus, R. R. Wittekind, 1972 .

Pyrazolo[5,1-b]quinazolin-9-ones: a new series of antiallergic agents.

J. Sircar, T. Capiris, D. J. Herzig, 1981, Journal of medicinal chemistry.

Structure−Activity Relationships of Pregabalin and Analogues That Target the α2-δ Protein

T. Heffner, A. Thorpe, L. Wise, 2005 .

Chromeno[3,4-c]pyridin-5-ones: selective human dopamine D4 receptor antagonists as potential antipsychotic agents.

T. Heffner, D. T. Connor, P. Unangst, 1997, Journal of medicinal chemistry.

Reactions of 2H‐3,1‐benzoxazine‐2,4‐(1H)dione (isatoic anhydride) with anions of 1,4‐dihydro‐5H‐pyrazol‐5‐ones: Synthesis of pyrazolo[5,1‐b]quinazolin‐9‐ones

J. Sircar, T. Capiris, S. Kesten, 1981 .

Nonsteroidal antiinflammatory drug hydroxamic acids. Dual inhibitors of both cyclooxygenase and 5-lipoxygenase.

R. D. Dyer, R. Dyer, D. Flynn, 1990, Journal of medicinal chemistry.

Synthesis of 4-hydroxy-N-[5-(hydroxymethyl)-3-isoxazolyl]-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide and [(5-methyl-3-isoxazolyl)amino]oxoacetic acid. Major metabolites of isoxicam

J. Sircar, T. Capiris, C. F. Schwender, 1985 .

Synthesis of 4-Hydroxy-N-[5-(hydroxymethyl)-3-isoxazolyl]-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-Dioxide and [(5-Methyl-3-isoxazolyl)amino]oxoacetic Acid. Major Metabolites of Isoxicam.

J. Sircar, T. Capiris, C. F. Schwender, 1986 .

Hydroxylamine analogs of 2,6-di-t-butylphenols: dual inhibitors of cyclooxygenase and 5-lipoxygenase or selective 5-lipoxygenase inhibitors.

R. D. Dyer, R. Dyer, D. Bornemeier, 1995, Bioorganic & medicinal chemistry.

Carboxylate bioisosteres of gabapentin.

A. El‐Kattan, S. Osborne, J. Bryans, 2006, Bioorganic & medicinal chemistry letters.