Ucb Pharma, S.a.

Stephen Robert Mack

Rikki Peter Alexander

Alan Findlay Haughan

Andrew Sharpe

Julien Alistair Brown

Christopher Lowe

Verity Margaret Sabin

George Martin Buckley

Karen Viviane Lucile Crépy

William Ross Pitt

Marianna Dilani Richard

Laura Jane Tait

Natasha Kinsella

Graham John Warrellow

Daniel Christopher Brookings

Roland W Bürli

Stephen Brand

Stuart Bailey

Helen Tracey Horsley

Richard Jeremy Franklin

Daniel Rees Allen

Anne Marie Foley

Andrew James Ratcliffe

Pavandeep Singh Aujla

Christopher James Lock

Trevor Morgan

Kerry Jenkins

Sophie Caroline Williams

William Mark Jones

Bénédicte Irma Léonce Frédérique Lallemand

Patrick Marie Ghislain Pasau

David Jonathan Phillips

Benjamin Garfield Perry

John Richard Davenport

A series of heteroaryl-substituted quinoxaline and quinoline derivatives, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions, said substituted derivatives having the general formula 

Quinoxaline and quinoline derivatives as kinase inhibitors

A series of 5,6-dihydro-1-benzothiophen-7(4H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

Fused thiophene derivatives as kinase inhibitors

A series of 6,7-dihydro[1,3]thiazolo[5,4-c]pyridin-4(5H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

Fused thiazole derivatives as kinase inhibitors

A series of thiazole derivatives which are substituted in the 2-position by a substituted morpholin-4-yl moiety, being selective inhibitors of P13 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

Thiazole derivatives as kinase inhibitors

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Slough, United Kingdom

Stephen Robert Mack