P. Owen

发表

Identification of a novel orally bioavailable ERK5 inhibitor with selectivity over p38α and BRD4.

M. Noble, J. Endicott, S. Cook, 2019, European journal of medicinal chemistry.

Discovery of potent inhibitors of the lysophospholipase autotaxin.

H. Ovaa, A. Turnbull, W. Moolenaar, 2016, Bioorganic & medicinal chemistry letters.

Synthesis and Lewis acidity of triorganosilyl and triorganostannyl esters of orthoboric, metaboric, and arylboronic acids

M. Beckett, P. Owen, K. Varma, 1999 .

3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic Acids: highly potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase AKR1C3.

W. Denny, A. Turnbull, D. G. Brooke, 2012, Journal of medicinal chemistry.

π-Bonding in B–O ring species: Lewis acidity of Me3B3O3, synthesis of amine Me3B3O3 adducts, and the crystal and molecular structure of Me3B3O3.NH2iBu·MeB(OH)2

M. Beckett, M. Hursthouse, M. Light, 1999 .

cyclo-Boratrisiloxane and cyclo-diboratetrasiloxane derivatives and their reactions with amines: crystal and molecular structure of (p-BrC6H4BO)2(Ph2SiO)2

D. Hibbs, M. Beckett, M. Hursthouse, 2000 .

Synthesis and Characterisation of Amine Adducts of Tri(4-bromophenyl) boroxine, Tri(3-nitrophenyl)boroxine, and Tri(3-aminophenyl)boroxine; Molecular Structure of 3-Picoline·tri(4-bromophenyl)boroxine

D. Hibbs, M. Beckett, M. Hursthouse, 1998 .

3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic acids; a New Class of Highly Potent and Selective Inhibitors of the Type 5 17-beta-hydroxysteroid Dehydrogenase AKR1C3

W. Denny, A. Turnbull, D. G. Brooke, 2012 .

3-(3,4-Dihydroisoquinolin-2(1H)-ylsulfonyl)benzoic acids; a New Class of Highly Potent and Selective Inhibitors of the Type 5 17-beta-hydroxysteroid Dehydrogenase AKR1C3

W. Denny, A. Turnbull, D. G. Brooke, 2012 .