T. Deegan

Identification of amidoheteroaryls as potent inhibitors of mutant (V600E) B-Raf kinase with in vivo activity.

David A. Scott, P. Lyne, L. Drew, 2009, Bioorganic & medicinal chemistry letters.

Discovery of (+)-N-(3-aminopropyl)-N-[1-(5-benzyl-3-methyl-4-oxo-[1,2]thiazolo[5,4-d]pyrimidin-6-yl)-2-methylpropyl]-4-methylbenzamide (AZD4877), a kinesin spindle protein inhibitor and potential anticancer agent.

L. Ronco, V. Oza, D. Huszar, 2011, Journal of medicinal chemistry.

Parallel synthesis of 1,2,4-oxadiazoles using CDI activation.

J. Porco, T. J. Nitz, T. Deegan, 1999, Bioorganic & medicinal chemistry letters.

Pyridyl and thiazolyl bisamide CSF-1R inhibitors for the treatment of cancer.

David A. Scott, P. Lyne, B. Aquila, 2008, Bioorganic & medicinal chemistry letters.

On the Development of New Poly(styrene-oxyethylene) Graft Copolymer Resin Supports for Solid-Phase Organic Synthesis

J. Labadie, T. Deegan, O. W. Gooding, 1999 .

Discovery and Optimization of a Novel Series of Highly Selective JAK1 Kinase Inhibitors.

C. Chuaqui, A. Ferguson, P. Lyne, 2018, Journal of medicinal chemistry.

Discovery of potent KIFC1 inhibitors using a method of integrated high-throughput synthesis and screening.

E. Hennessy, C. Chuaqui, Nancy Su, 2014, Journal of medicinal chemistry.

Discovery of potent KIFC1 inhibitors using a method of integrated high-throughput synthesis and screening.

E. Hennessy, C. Chuaqui, Nancy Su, 2014, Journal of medicinal chemistry.