IP Library Granted Patent US 9,402,850
Granted Patent B2
US 9,402,850 · App. 14/709,580 · Granted Aug 2, 2016

BAX agonist, compositions, and methods related thereto

Inventors: Xingming Deng (Lilburn, GA); Jia Zhou (League City, TX); Chunyong Ding (Galveston, TX)
Assignees: Emory University; Board of Regents, The University of Texas System
A61K31/5375A61K31/05A61K31/085A61K31/138A61K31/404A61K31/44A61K31/4412A61K31/4465A61K31/495A61K45/06C07C205/11C07C205/25C07C205/35C07C211/52C07C215/88C07C217/20C07C217/26C07C217/60C07C217/94C07C233/18C07C233/25C07C233/80C07C271/16C07C309/65C07C311/21C07D209/10C07D209/12C07D211/46C07D213/61C07D213/64C07D213/643C07D213/73C07D213/74C07D295/088C07D295/185C07D295/26C07C2101/02C07C2103/18
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Quick Facts
Patent No.
US 9,402,850
App. No.
14/709,580
Granted
Aug 2, 2016
Kind
B2
Abstract

The disclosure relates to BAX activators and therapeutic uses relates thereto. In certain embodiments, the disclosure relates to methods of treating or preventing cancer, such as lung cancer, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a compound disclosed herein or pharmaceutically acceptable salt to a subject in need thereof.

Claims (22)

1. A method of treating lung cancer comprising administering an effective amount of a compound of Formula IB, to a subject in need thereof,

or salt thereof wherein,

Z is O, S, CH 2 , or NH;

W is hydroxy, amino, alkylamino, dialkylamino, aryl, or heterocyclyl wherein W is optionally substituted with one or more R 11 ;

R 1 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each individually and independently hydrogen, alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 1 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are optionally substituted with one or more, the same or different R 10 ;

R 2 is nitro or amino wherein R 2 is optionally substituted with one or more, the same or different R 10 ;

R 10 is alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 10 is optionally substituted with one or more, the same or different R 11 ;

R 11 is alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 11 is optionally substituted with one or more, the same or different R 12 ; and

R 12 is halogen, nitro, cyano, hydroxy, trifluoromethoxy, trifluoromethyl, amino, formyl, carboxy, carbamoyl, mercapto, sulfamoyl, methyl, ethyl, methoxy, ethoxy, acetyl, acetoxy, methylamino, ethylamino, dimethylamino, diethylamino, N-methyl-N-ethylamino, acetylamino, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-methyl-N-ethylcarbamoyl, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, mesyl, ethylsulfonyl, methoxycarbonyl, ethoxycarbonyl, N-methylsulfamoyl, N-ethylsulfamoyl, N,N-dimethylsulfamoyl, N,N-diethylsulfamoyl, N-methyl-N-ethylsulfamoyl, carbocyclyl, aryl, or heterocyclyl.

2. The compound claim 1 , wherein R 2 is nitro.

3. The compound of claim 1 , selected from the group:

4-{2-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-morpholine;

1-{2-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-piperazine;

2-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethanol;

2-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethylamine;

4-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-piperidine;

1-(4-Fluoro-benzenesulfonyl)-4-{2-[2-(2-nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-piperazine;

1-(4-{2-[2-(2-Nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-piperazin-1-yl)-ethanone;

1-Cyclopropanesulfonyl-4-{2-[2-(2-nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-piperazine; and

1-Methanesulfonyl-4-{2-[2-(2-nitro-fluoren-9-ylidenemethyl)-phenoxy]-ethyl}-piperazine or salts thereof.

4. The method of claim 1 , wherein the compound is administered in combination with a second chemotherapeutic agent.

5. The method of claim 4 , wherein the second chemotherapeutic agent is gefitinib, erlotinib, docetaxel, cis-platin, 5-fluorouracil, gemcitabine, tegafur, raltitrexed, methotrexate, cytosine arabinoside, hydroxyurea, adriamycin, bleomycin, doxorubicin, daunomycin, epirubicin, idarubicin, mitomycin-C, dactinomycin, mithramycin, vincristine, vinblastine, vindesine, vinorelbine taxol, taxotere, etoposide, teniposide, amsacrine, topotecan, camptothecin, bortezomib, anegrilide, tamoxifen, toremifene, raloxifene, droloxifene, iodoxyfene fulvestrant, bicalutamide, flutamide, nilutamide, cyproterone, goserelin, leuprorelin, buserelin, megestrol, anastrozole, letrozole, vorazole, exemestane, finasteride, marimastat, trastuzumab, cetuximab, dasatinib, imatinib, bevacizumab, combretastatin, thalidomide, and/or lenalidomide or combinations thereof.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 13, 2016
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 038964/0366 →
Continuity (4)
Continuation 14239177
Provisional Application 61525249 · Aug 19, 2011
Provisional Application 61648887 · May 18, 2012
Related Publication 20150250793A1 · Sep 10, 2015