The present invention relates to novel phosphate isosteres. The invention relates to compounds having a sulfhydantoin or a reverse sulfhydantoin moiety, uses thereof, and related methods. The present invention relates to compounds of formula I or II:
1
or pharmaceutically acceptable salts thereof; wherein Q, T, m, and X are as described herein. These compounds are inhibitors of phosphatases, particularly inhibitors of SHP-2. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of utilizing these compounds and compositions in the treatment of various phosphatase-mediated diseases.
本发明涉及新型
磷酸酯异构体。本发明涉及具有
硫代
肼或反
硫代
肼基团的化合物,以及它们的用途和相关方法。本发明涉及公式I或II的化合物:1或其药学上可接受的盐;其中Q,T,m和X如本文所述。这些化合物是
磷酸酯酶的
抑制剂,特别是SHP-2的
抑制剂。本发明还提供包括本发明中化合物的药学上可接受的组合物,以及利用这些化合物和组合物治疗各种
磷酸酯酶介导的疾病的方法。