发明名称 Substituted imidazopyridines as HDM2 inhibitors
摘要 The present invention provides substituted imidazopyridines as described herein or a pharmaceutically acceptable salt or solvate thereof. The representative compounds are useful as inhibitors of the HDM2 protein. Also disclosed are pharmaceutical compositions comprising the above compounds and potential methods of treating cancer using the same.
申请公布号 US8962611(B2) 申请公布日期 2015.02.24
申请号 US201414465577 申请日期 2014.08.21
申请人 Merck Sharp & Dohme Corp. 发明人 Christopher Matthew P.;Fradera Llinas Francesc Xavier;Machacek Michelle;Martinez Michelle;Reutershan Michael Hale;Shizuka Manami;Sun Binyuan;Thompson Christopher Francis;Trotter B. Wesley;Voss Matthew E.;Altman Michael D.;Bogen Stephane L.;Doll Ronald J.
分类号 A61K31/553;C07D471/04;C07D519/00 主分类号 A61K31/553
代理机构 代理人 Zhao Yong;Su Li;Ginkel Laura M.
主权项 1. A method of treating cancer in a patient wherein the cancer is selected from the group consisting of lymphoma, acute myeloid leukemia, acute lymphoblastic leukemia, multiple myeloma, melanoma, sarcoma, liposarcoma, glioblastoma, and colorectal cancer and cancer of the breast, stomach, prostate, endometrium, kidney, bladder, colon, ovary and lung, comprising the step of administering to the patient an effective amount of a compound selected from the group consisting of: or a stereoisomer thereof; or a pharmaceutically acceptable salt thereof; or a pharmaceutically acceptable salt of the stereoisomer thereof.
地址 Rahway NJ US