US2012283287A1PendingUtilityA1

Certain chemical entities, compositions, and methods

Assignee: QIAN XIANGPINGPriority: May 6, 2004Filed: Apr 9, 2012Published: Nov 8, 2012
Est. expiryMay 6, 2024(expired)· nominal 20-yr term from priority
C07C 2601/02C07C 307/10C07C 257/08C07D 471/04C07D 233/70C07D 263/32C07C 235/52C07D 277/42C07D 261/08C07D 207/273C07D 413/06C07D 235/26C07D 235/18C07D 295/155C07D 271/10C07D 271/07C07C 2601/14C07C 275/40A61P 31/10A61P 37/00C07D 333/38C07D 233/64C07D 263/10C07C 235/48C07D 211/76C07C 271/20C07F 9/6506C07D 271/06C07D 285/02C07C 311/37C07C 281/06C07C 255/60C07D 231/12C07D 257/04C07D 285/125C07C 237/22C07C 271/24C07D 271/113C07D 211/34C07D 498/04A61P 35/00C07C 271/28C07D 249/08C07C 275/42C07C 255/57C07D 403/10C07D 235/06C07D 403/12C07D 277/56C07C 311/46C07C 255/59C07C 275/26A61P 9/00C07D 263/12C07D 233/61C07D 239/36C07D 213/30C07D 231/14C07D 277/30C07C 259/18C07C 235/50C07C 257/18C07D 295/145C07F 9/6561C07D 235/16
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Claims

Abstract

Compounds useful for treating cellular proliferative diseases and disorders by modulating the activity of one or more mitotic kinesins are disclosed.

Claims

exact text as granted — not AI-modified
1 - 46 . (canceled) 
     
     
         47 . A method of treating a solid tumor in a subject, the method comprising administering to the subject a therapeutically effective amount of N-(2-(2-dimethylamino-acetylamino)-1-{4-[8-(1-hydroxy-ethyl)-imidazo[1,2-a]pyridin-2-yl]-benzyl}-ethyl)-3-chloro-4-isopropoxy-benzamide, or a pharmaceutically acceptable salt thereof. 
     
     
         48 . The method of  claim 47 , comprising administering to the subject a compound having the formula: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof. 
       
     
     
         49 . The method of  claim 47 , wherein the N-(2-(2-dimethylamino-acetylamino)-1-{4-[8-(1-hydroxy-ethyl)-imidazo[1,2-a]pyridin-2-yl]-benzyl}-ethyl)-3-chloro-4-isopropoxy-benzamide, or a pharmaceutically acceptable salt thereof, is formulated into a pharmaceutical composition comprising at least one pharmaceutical excipient. 
     
     
         50 . The method of  claim 49 , wherein the pharmaceutical composition is formulated for oral administration. 
     
     
         51 . The method of  claim 49 , wherein the pharmaceutical composition is formulated for intravenous administration. 
     
     
         52 . The method of  claim 47 , wherein the solid tumor is a cancerous tumor, wherein the cancerous tumor is selected from colon cancer, breast cancer, ovarian cancer, prostate cancer, lung cancer, neuroblastoma, Ewing sarcoma, and rhabdomyosarcoma.

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