Thiadiazoline derivative
    1.
    发明公开
    Thiadiazoline derivative 有权
    噻二唑啉衍生物zur Behandlung von Krebs

    公开(公告)号:EP1847534A2

    公开(公告)日:2007-10-24

    申请号:EP07015426.5

    申请日:2002-12-11

    摘要: (wherein R 1 and R 4 are the same or different and each represents a hydrogen atom, substituted or unsubstituted lower alkyl, substituted or unsubstituted lower alkynyl, substituted or unsubstituted lower alkenyl, or the like; R 5 represents a substituted or unsubstituted heterocyclic group, substituted or unsubstituted aryl, or the like; R 2 represents -C(=W)R 6 or the like; R 3 represents a hydrogen atom, -C(=W A )R 6A , or the like)
    Antitumor agents which comprises a thiadiazoline derivative represented by the aforementioned general formula (I) or a pharmacologically acceptable salt thereof as an active ingredient are provided.

    摘要翻译: (其中R 1和R 4相同或不同,各自表示氢原子,取代或未取代的低级烷基,取代或未取代的低级炔基,取代或未取代的低级链烯基等; R 5表示取代或未取代的杂环基 取代或未取代的芳基等; R 2表示-C(= W)R 6等; R 3表示氢原子,-C(= WA)R 6A等)抗肿瘤剂,其包含 提供由上述通式(I)表示的噻二唑啉衍生物或其药理学上可接受的盐作为有效成分。

    Mitotic kinesin inhibitor
    3.
    发明公开
    Mitotic kinesin inhibitor 有权
    M档,驱动蛋白抑制剂

    公开(公告)号:EP2327702A1

    公开(公告)日:2011-06-01

    申请号:EP11158215.1

    申请日:2004-04-16

    摘要: A mitotic kinesin Eg5 inhibitor which comprises a thiadiazoline derivative represented by the general formula (I) or a pharmacologically acceptable salt thereof as an active ingredient:

    [wherein R 1 represents a hydrogen atom and the like, R 2 represents a hydrogen atom, -C(=W)R 6 (wherein W represents an oxygen atom or a sulfur atom, and R 6 represents substituted or unsubstituted lower alkyl and the like) and the like, R 3 represents -C(=Z)R 19 (wherein Z represents an oxygen atom or a sulfur atom, and R 19 represents substituted or unsubstituted lower alkyl and the like) and the like, R 4 represents substituted or unsubstituted lower alkyl and the like, and R 5 represents substituted or unsubstituted aryl and the like] and the like are provided.

    摘要翻译: 一种有丝分裂驱动蛋白Eg5抑制剂,其包含由通式(I)表示的噻二唑啉衍生物或其药理学上可接受的盐作为活性成分:[其中R 1表示氢原子等,R 2表示氢原子,-C (= W)R 6(其中W表示氧原子或硫原子,R 6表示取代或未取代的低级烷基等)等,R 3表示-C(= Z)R 19(其中Z表示 氧原子或硫原子,R 19表示取代或未取代的低级烷基等)等,R 4表示取代或未取代的低级烷基等,R 5表示取代或未取代的芳基等]和 提供类似物。