Pharmaceutical compounds

US8399442B2 · kind B2 · utility

Assignee

• ASTEX THERAPEUTICS LIMITED · GB

Inventors

• Valerio Berdini · Cambridge, GB
• Jayne Elizabeth Curry · Cambridge, GB
• Neil James Gallagher · Basel, CH
• Adrian Liam Gill · Atherton, US
• John Francis Lyons · London, GB

Key dates

• Filing date: Dec 29, 2006
• Grant date: Mar 19, 2013
• Expiry date: May 16, 2029

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C07D513/04
• WIPO field: Pharmaceuticals
• WIPO sector: Chemistry

Abstract

A method for the treatment of: A. a disease state or condition mediated by a kinase wh ich is BCR-abl, VEGFR, PDGFR, EGFR, FLT3, JAK, C-abl, PDK1, Chk, FGFR, Ret, Eph, or Src; or B. a cancer in which the cancer cells thereof contain a drug resistant kinase mutation which is: (a) a threonine gatekeeper mutation; or (b) a drug-resistant gatekeeper mutation; or (c) an imatinib resistant mutation; or (d) a nilotinib resistant mutation; or (e) a dasatinib resistant mutation; or (f) a T670l mutation in KIT; or (g) a T674l mutation in PDGFR; or (h) T790M mutation in EGFR; or (i) a T315l mutation in abl; or C. a cancer which expresses a mutated molecular target which is a mutated form of BCRabl, c-kit, PDGF, EGF receptor or ErbB2; which method comprises administering to a patient in need thereof a therapeutically effective amount of a compound of the formula (l or l′): or a salt, solvate, tautomer or N-oxide thereof.