IP Library Granted Patent US 9,975,868
Granted Patent B2
US 9,975,868 · App. 15/593,654 · Granted May 22, 2018

7,8-dihydoxyflavone and 7,8-substituted flavone derivatives, compositions, and methods related thereto

Inventor: Keqiang Ye (Lilburn, GA)
Assignee: Emory University
C07D311/30A61K31/352A61K45/06C07D311/28C07D311/36C07D311/38
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Quick Facts
Patent No.
US 9,975,868
App. No.
15/593,654
Granted
May 22, 2018
Kind
B2
Abstract

In certain embodiments, the disclosure relates to 7,8-dihydoxyflavone and 7,8-substituted flavone derivatives, such as those described by formula provided herein, pharmaceutical compositions, and methods related thereto. In certain embodiments, the disclosure relates to methods of treating or preventing diseases or conditions related to BDNF and TrkB activity, such as psychiatric disorders, depression, post-traumatic stress disorder, and autism spectrum disorders, stroke, Rett syndrome, Parkinson's disease, and Alzheimer's disease by administering effective amounts of pharmaceutical compositions comprising compounds disclosed herein to a subject in need thereof. In certain embodiments, it is contemplated that the 7,8-substituted flavone derivatives disclosed herein are prodrugs of 7,8-dihydoxyflavone and analogs.

Claims (32)

1. A method of treating a BDNF and TrkB related disease or condition comprising administering an effective amount of a pharmaceutical composition to a subject in need thereof, wherein the pharmaceutical composition comprises a compound of Formula I:

or a salt thereof, wherein:

X is O, S, or NH;

U and Y are each O, S, NH, Nalkyl, or CH 2 ;

Z is hydrogen, amino, diaminoalkyl, or heterocyclyl optionally substituted with one or more, the same or different, R 15 ;

R 1 is alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkyl sulfonyl, arylsulfonyl, carbocyclyl, or aryl, wherein R 1 is optionally substituted with one or more, the same or different, R 15 ;

R 2 is alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkyl sulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 2 is optionally substituted with one or more, the same or different, R 15 ;

R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are each individually and independently hydrogen, alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkyl sulfonyl, aryl sulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are optionally substituted with one or more, the same or different, R 15 ;

R 15 is independently selected alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, alkylthio, alkylamino, (alkyl) 2 amino, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, or aryl, wherein R 15 is optionally substituted with one or more, the same or different, R 16 ; and

R 16 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, ethyl sulfonyl, methoxycarbonyl, ethoxycarbonyl, N-methylsulfamoyl, N-ethylsulfamoyl, N,N-dimethylsulfamoyl, N,N-diethylsulfamoyl, N-methyl-N-ethylsulfamoyl, carbocyclyl, aryl, or heterocyclyl; and

a pharmaceutically acceptable excipient,

wherein the disease or condition is depression, schizophrenia, obsessive-compulsive disorder, anorexia nervosa, bulimia nervosa, anxiety, amyotrophic lateral sclerosis, Autism spectrum disorders, post-traumatic stress disorder, Alzheimer's disease, Huntington's disease, Rett syndrome, epilepsy, Parkinson's disease, dementia, diabetic neuropathy, peripheral neuropathy, or stroke.

2. The method of claim 1 , wherein the subject is diagnosed with, exhibiting symptoms of, or at risk of the disease or condition.

3. The method of claim 1 , wherein the disease is depression and the pharmaceutical composition is administered in combination with an anti-depressant.

4. The method of claim 3 , wherein the anti-depressant is a selective serotonin reuptake inhibitor, a serotonin-norepinephrine reuptake inhibitor, a noradrenergic and specific serotonergic antidepressant, a norepinephrine reuptake inhibitor, a norepinephrine-dopamine reuptake inhibitor, a selective serotonin reuptake enhancer, a norepinephrine-dopamine disinhibitor, a tricyclic antidepressant, or a monoamine oxidase inhibitor.

5. The method of claim 1 , wherein U and Y are NH or Nalkyl.

6. The method of claim 1 , wherein U and Y are oxygen.

7. The method of claim 1 , wherein R 1 and R 2 are alkyl.

8. The method of claim 1 , wherein the compound is selected from:

4-oxo-2-phenyl-4H-chromene-7,8-diyl bis(methylcarbamate);

4-oxo-2-phenyl-4H-chromene-7,8-diyl dipropionate;

diethyl (4-oxo-2-phenyl-4H-chromene-7,8-diyl) dicarbonate;

4-oxo-2-phenyl-4H-chromene-7,8-diyl bis(ethylcarbamate);

4-oxo-2-phenyl-4H-chromene-7,8-diyl bis(dimethylcarbamate); and

4-oxo-2-phenyl-4H-chromene-7,8-diyl bis(3-methylbutanoate), or a salt thereof.

9. The method of claim 1 , wherein the disease or condition is Alzheimer's disease.

10. The method of claim 1 , wherein the disease or condition is Parkinson's disease.

11. The method of claim 1 , wherein the disease or condition is depression.

12. The method of claim 1 , wherein the disease or condition is Huntington's disease.

13. The method of claim 3 , wherein the anti-depressant is citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, vilazodone, desvenlafaxine, duloxetine, milnacipran, venlafaxine, mianserin, mirtazapine, atomoxetine, mazindol, reboxetine, viloxazine, bupropion, tianeptine, amineptine, agomelatine, amitriptyline, clomipramine, doxepin, imipramine, trimipramine, desipramine, nortriptyline, protriptyline, isocarboxazid, moclobemide, phenelzine, selegiline, or tranylcypromine.

14. A method of treating a BDNF and TrkB related disease or condition comprising administering an effective amount of a pharmaceutical composition to a subject in need thereof, wherein the pharmaceutical composition comprises 4-oxo-2-phenyl-4H-chromene-7,8-diyl bis(2,2-dimethylpropanoate) and a pharmaceutically acceptable excipient,

wherein the disease or condition is depression, schizophrenia, obsessive-compulsive disorder, anorexia nervosa, bulimia nervosa, anxiety, amyotrophic lateral sclerosis, autism spectrum disorders, post-traumatic stress disorder, Alzheimer's disease, Huntington's disease, Rett syndrome, epilepsy, Parkinson's disease, dementia, diabetic neuropathy, peripheral neuropathy, or stroke.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2018
From: YE, KEQIANG
To: EMORY UNIVERSITY
Reel/Frame 045768/0578 →
CONFIRMATORY LICENSE Recorded Apr 6, 2018
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045458/0891 →
Continuity (4)
Division 14437232
Provisional Application 61845399 · Jul 12, 2013
Provisional Application 61722339 · Nov 5, 2012
Related Publication 20170305876A1 · Oct 26, 2017