IP Library › Granted Patent US 12,391,659
Granted Patent B2
US 12,391,659 · App. 17/392,036 · Granted Aug 19, 2025

Benzothiazole and related compounds

Inventors: Stella Sarraf (Beverly Hills, CA); Vincent F. Simmon (San Diego, CA); Gerald F. Swiss (San Diego, CA)
Assignee: Spinogenix, Inc.
C07D277/66A61P25/28
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Quick Facts
Patent No.
US 12,391,659
App. No.
17/392,036
Granted
Aug 19, 2025
Kind
B2
Abstract

Disclosed are compounds that promote spinogenesis, are capable of reducing the neural toxicity of beta-amyloid peptides, and/or reduce the symptoms of traumatic brain injury in a patient.

Claims (45)

1. A pharmaceutical composition comprising a compound according to Formula VII:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

subscripts n and p are each independently selected from 0, 1, or 2;

subscript q is an integer selected from 2, 3, and 5-8; and

each R 1 and R 2 are independently selected from the group consisting of halo, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, acyl, acylamino, aminocarbonyl, aminosulfonyl, amino, substituted amino, aryl, substituted aryl, carboxyl, carboxyl esters, cyano, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, hydroxyl, sulfonyl, substituted sulfonyl, thiol, thioalkyl, and nitro,

and one or more pharmaceutically acceptable excipients.

2. The pharmaceutical composition of claim 1 , wherein:

subscript q is an integer selected from 3, 5, or 6;

R 1 is selected from the group consisting of halo, —OH, —CN, phenyl, —CHCH 2 , —COCH 3 , —COOCH 3 , —CH 2 SO 2 NH 2 , —NHCOCH 3 , —N(CH 3 ) 2 , —SCH 3 , and —SO 2 NH 2 ; and

R 2 is selected from the group consisting of halo, —CH 3 , —CH 2 CH 3 , cyclopentyl, —CF 3 , —CN, —CHCH 2 , —CH 2 CHCH 2 , phenyl, —CO 2 H, —CH 2 CO 2 H, —CH 2 CONH 2 , —COOCH 3 , —COCH 3 , —(CH 2 ) 2 OCH 3 , —CONH 2 , —CON(CH 3 ) 2 , —CH 2 SO 2 N(CH 3 ) 2 , —OCH 3 , —OCF 3 , —OCH(CH 3 ) 2 , —N(CH 3 ) 2 , —NHCOCH 3 , —NO 2 , —SCH 3 , —SO 2 CH 3 , and —SO 2 N(CH 3 ) 2 .

3. The pharmaceutical composition of claim 1 , wherein subscripts n and p are independently selected from 0 or 1, provided that subscripts n and p are not both 1.

4. The pharmaceutical composition of claim 1 , wherein the compound is:

5. The pharmaceutical composition of claim 1 , wherein:

R 1 is selected from the group consisting of halo, —CH 3 , —OCH 3 , phenyl, and —CN; and

R 2 is selected from the group consisting of halo, —CH 3 , —CF 3 , —OCH 3 , —OCF 3 , CHCH 2 , —CH 2 CHCH 2 , phenyl, and —NO 2 .

6. The pharmaceutical composition of claim 1 , wherein the compound of formula VII is represented by Formula VIIa:

wherein:

subscript q is 5 or 6;

R 3 , R 4 , R 5 , and R 6 are independently selected from the group consisting of hydrogen, halo, CH 3 , and —OCH 3 ; and

R 7 , R 8 , R 9 and R 10 are independently selected from the group consisting of hydrogen, halo, CH 3 , —CF 3 , —OCH 3 , —OCF 3 , phenyl, and —NO 2 ;

wherein at least six of R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are hydrogen.

7. A method for increasing dendritic spine density of neurons comprising contacting the neurons with a pharmaceutical composition of claim 1 under conditions sufficient to increase dendritic spine density of neurons.

8. The method of claim 7 , wherein the method is conducted subsequent to a patient receiving a traumatic brain injury.

9. A method for decreasing neurotoxicity of beta-amyloid peptides to neurons comprising contacting the beta-amyloid peptides with a pharmaceutical composition of claim 1 under conditions sufficient to decrease the neurotoxicity of the beta-amyloid peptides.

10. A method for reducing the symptoms of traumatic brain injury in a patient suffering from traumatic brain injury by administering the pharmaceutical composition of claim 1 under conditions sufficient to reduce the symptoms of traumatic brain injury.

11. The method of claim 10 , wherein the method is conducted within about 0 to 72 hours of the traumatic brain injury.

12. The method of claim 10 , wherein the reduction of the symptoms of trauma is measured by an improvement in the performance of one or more functional domains by at least 20% to 30% within about 7 days of treatment as compared to the performance of the one or more functional domains measured prior to treatment but after injury.

13. A method for increasing dendritic spine density of neurons comprising contacting the neurons with a compound according to Formula VII:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

subscripts n and p are each independently selected from 0, 1, or 2;

subscript q is an integer selected from 2, 3, and 5-8; and

each R 1 and R 2 are independently selected from the group consisting of halo, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, acyl, acylamino, aminocarbonyl, aminosulfonyl, amino, substituted amino, aryl, substituted aryl, carboxyl, carboxyl esters, cyano, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, hydroxyl, sulfonyl, substituted sulfonyl, thiol, thioalkyl, and nitro, under conditions sufficient to increase dendritic spine density of neurons.

14. The method of claim 13 , wherein the method is conducted subsequent to a patient receiving a traumatic brain injury.

15. A method for decreasing neurotoxicity of beta-amyloid peptides to neurons comprising contacting the beta-amyloid peptides with a compound according to Formula VII:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

subscripts n and p are each independently selected from 0, 1, or 2;

subscript q is an integer selected from 2, 3, and 5-8; and

each R 1 and R 2 are independently selected from the group consisting of halo, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, acyl, acylamino, aminocarbonyl, aminosulfonyl, amino, substituted amino, aryl, substituted aryl, carboxyl, carboxyl esters, cyano, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, hydroxyl, sulfonyl, substituted sulfonyl, thiol, thioalkyl, and nitro, under conditions sufficient to decrease the neurotoxicity of the beta-amyloid peptides.

16. A method for reducing the symptoms of traumatic brain injury in a patient suffering from traumatic brain injury by administering a compound according to Formula VII:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

subscripts n and p are each independently selected from 0, 1, or 2;

subscript q is an integer selected from 2, 3, and 5-8; and

each R 1 and R 2 are independently selected from the group consisting of halo, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, acyl, acylamino, aminocarbonyl, aminosulfonyl, amino, substituted amino, aryl, substituted aryl, carboxyl, carboxyl esters, cyano, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclyl, substituted heterocyclyl, hydroxyl, sulfonyl, substituted sulfonyl, thiol, thioalkyl, and nitro, under conditions sufficient to reduce the symptoms of traumatic brain injury.

17. The method of claim 16 , wherein the method is conducted within about 0 to 72 hours of the traumatic brain injury.

18. The method of claim 16 , wherein the reduction of the symptoms of trauma is measured by an improvement in the performance of one or more functional domains by at least 20% to 30% within about 7 days of treatment as compared to the performance of the one or more functional domains measured prior to treatment but after injury.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE CONVEYING PARTY DATA PREVIOUSLY RECORDED AT REEL: 71699 FRAME: 450. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Oct 13, 2025
From: SARRAF, STELLA; SIMMON, VINCENT F.; SWISS, GERALD F.
To: SPINOGENIX, INC.
Reel/Frame 073078/0546 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2025
From: SARRAF, STELLA; SIMMONS, VINCENT F.; SWISS, GERALD F.
To: SPINOGENIX, INC.
Reel/Frame 071699/0450 →
Continuity (3)
Continuation 16635872
Provisional Application 62540311 · Aug 2, 2017
Related Publication 20220017477A1 · Jan 20, 2022
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