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    • 8. 发明申请
    • Quinoneimines of malonic acid diamides
    • 丙二酸二酰胺喹啉酮
    • US20070112072A1
    • 2007-05-17
    • US10565506
    • 2004-07-23
    • David DekkersLucien AardenJanna Ten Brinke
    • David DekkersLucien AardenJanna Ten Brinke
    • A61K31/16C07C251/22
    • C07C251/28A23L33/10C07C235/16C07C323/41Y02P20/55
    • The present invention provides optionally substituted compounds of the formula I or salts thereof; wherein R1 is O or S when double bonded to the ring or is OH, SH, or a protected equivalent, when single bonded to the ring, R2 is hydrogen or more preferably an C1-C10 organic group attached by a carbon atom, X is H, O, OO, S or SS R3 is absent where X═H, is hydrogen or is a hydroxyl or thiol protecting group, R4 is a hetero- or preferably homo-cyclic aryl group, optionally substituted with a further group R5 and groups T1 are each, independently, absent, hydrogen or an S—R6 group, where any/each R6 is independently an organic group of molecular weight up to around 500 amu. The invention further provides a method for the synthesis of such compounds and a method of treatment comprising administering such compounds to a mammalian subject.
    • 本发明提供任选取代的式I化合物或其盐; 当双键键合到环上时,R 1是O或S,或者是OH,SH或被保护的等价物,当单键与环结合时,R 2是氢或 更优选由碳原子连接的C 1 -C 10 - 有机基团,X是H,O,OO,S或SS R 3 在其中XH为氢或为羟基或硫醇保护基团时不存在,R 4为异或优选的高环芳基,任选被另外的基团R 5取代, 和基团T 1 1各自独立地不存在氢或SR 6 - 基团,其中任何/每个R 6独立地为 有机基团的分子量可达500 amu左右。 本发明进一步提供了一种合成这些化合物的方法和一种治疗方法,包括向哺乳动物受试者施用此类化合物。