S. Lautar

发表

DPP IV inhibitor blocks mescaline-induced scratching and amphetamine-induced hyperactivity in mice

W. Li, D. Ferraris, B. Slusher, 2005, Brain Research.

Design and synthesis of poly ADP-ribose polymerase-1 inhibitors. 2. Biological evaluation of aza-5[H]-phenanthridin-6-ones as potent, aqueous-soluble compounds for the treatment of ischemic injuries.

Jie Zhang, V. Kalish, Lisa T. Morgan, 2003, Journal of medicinal chemistry.

GPI 6150 prevents H(2)O(2) cytotoxicity by inhibiting poly(ADP-ribose) polymerase.

J. Zhang, J. Li, S. Lautar, 2000, Biochemical and biophysical research communications.

Design and synthesis of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. Part 4: biological evaluation of imidazobenzodiazepines as potent PARP-1 inhibitors for treatment of ischemic injuries.

Jie Zhang, V. Kalish, Lisa T. Morgan, 2003, Bioorganic & medicinal chemistry.

Azetidine-based inhibitors of dipeptidyl peptidase IV (DPP IV).

D. Ferraris, C. Rojas, B. Thomas, 2007, Current Topics in Medicinal Chemistry.

Design and synthesis of poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors. Part 3: In vitro evaluation of 1,3,4,5-tetrahydro-benzo[c][1,6]- and [c][1,7]-naphthyridin-6-ones.

Jie Zhang, V. Kalish, D. Ferraris, 2003, Bioorganic & medicinal chemistry letters.

Ketopyrrolidines and ketoazetidines as potent dipeptidyl peptidase IV (DPP IV) inhibitors.

V. Kalish, D. Ferraris, C. Rojas, 2004, Bioorganic & medicinal chemistry letters.

Ligand autoradiographic receptor screening: receptor cDNA expression in replicas of transfected COS cells.

G. Uhl, M. Rattray, S. Lautar, 1990, Brain research. Molecular brain research.

Synthesis of substituted 5[H]phenanthridin-6-ones as potent poly(ADP-ribose)polymerase-1 (PARP1) inhibitors.

J. Zhang, V. Kalish, D. Ferraris, 2001, Bioorganic & medicinal chemistry letters.

A yeast three-hybrid method to clone ternary protein complex components.

J. Zhang, S. Lautar, 1996, Analytical biochemistry.