Norman Peter
Norman Consulting , 18 Pink Lane, Burnham, Bucks, SL1 8JW , UK
Expert Opin Ther Pat. 2014 Mar;24(3):361-8. doi: 10.1517/13543776.2014.864637. Epub 2014 Jan 3.
Three patent applications, from two different companies, claim structurally novel Tyk2 inhibitors and their uses for the treatment of autoimmune diseases. In EP-2634185 Sareum claims 5-anilino-2-(2-halophenyl)-oxazole-4-carboxamide derivatives which are shown to be nanomolar potency Tyk2 inhibitors with 10 - 100-fold selectivity over JAK1, JAK2 and JAK3. Takeda's WO-2013125543 and WO-2013146963 claim two distinct structural classes of Tyk2 inhibitors. The first application claims inhibitors based on an unusual 1,5-dihydro-4H-pyrazolo[4,3-c]pyridine-4-one scaffold and the second claims 1-(2-arylaminopyrimidin-4-yl)-pyrrolidin-2-one derivatives. One example of the latter was shown to be orally active in an IL-23-induced inflammation model.
来自两家不同公司的三项专利申请,声称具有结构新颖的酪氨酸激酶2(Tyk2)抑制剂及其用于治疗自身免疫性疾病的用途。在欧洲专利EP - 2634185中,Sareum公司声称5 - 苯胺基 - 2 - (2 - 卤代苯基) - 恶唑 - 4 - 甲酰胺衍生物,这些衍生物被证明是纳摩尔效力的Tyk2抑制剂,对JAK1、JAK2和JAK3具有10至100倍的选择性。武田公司的WO - 2013125543和WO - 2013146963声称两种不同结构类型的Tyk2抑制剂。第一项申请声称基于一种不寻常的1,5 - 二氢 - 4H - 吡唑并[4,3 - c]吡啶 - 4 - 酮支架的抑制剂,第二项申请声称1 - (2 - 芳基氨基嘧啶 - 4 - 基) - 吡咯烷 - 2 - 酮衍生物。后者的一个例子在白细胞介素 - 23诱导的炎症模型中显示出口服活性。