IP Library Granted Patent US 11,332,464
Granted Patent B2
US 11,332,464 · App. 16/866,022 · Granted May 17, 2022

Inhibitors of lysine gingipain

Inventors: Andrei W. Konradi (Burlingame, CA); Stephen S. Dominy (Novato, CA); Casey Crawford Lynch (San Francisco, CA); Craig Coburn (San Rafael, CA); Joseph Vacca (Philadelphia, PA)
Assignee: CORTEXYME, INC.
C07D417/12C07C233/62C07C233/78C07C247/16C07C247/18C07D213/50C07D213/53C07D277/24C07D277/28C07D277/64C07D409/12C07B2200/07C07C2601/08
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Quick Facts
Patent No.
US 11,332,464
App. No.
16/866,022
Granted
May 17, 2022
Kind
B2
Abstract

The present invention relates generally to therapeutics targeting the bacterium Porphyromonas gingivalis , including its protease Lysine gingipain (Kgp), and their use for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease. In certain embodiments, the invention provides compounds according to Formula I, as described herein, and pharmaceutically acceptable salts thereof.

Claims (21)

1. A method for treating periodontal disease, the method comprising administering to a subject an effective amount of a compound according to the formula:

or a pharmaceutically acceptable salt thereof, wherein

Z is selected from the group consisting of benzothiazol-2-yl-carbonyl, pyridin-2-yl-carbonyl, and thiazol-2-yl-carbonyl; and

R 3 is selected from the group consisting of cyclohexyl, cyclopentyl, morpholino, phenyl, piperidinyl, pyridinyl, oxodihydropyridinyl, tetrahydrofuranyl, tetrahydropyranyl, 1,2,3,4-tetrahydronaphthyl, and thiazolyl,

wherein R 3 is optionally substituted with 1-3 members selected from the group consisting of methyl, methoxy, trifluoromethyl, acetyl, and —N 3 .

2. The method of claim 1 , wherein R 3 is selected from the group consisting of cyclohexyl; 1-methylcyclohexyl; 1-methoxycyclohexyl; cyclopentyl; morpholin-2-yl; 4-acetylmorpholin-2-yl; phenyl; 2-trifluoromethylphenyl; 3-azidophenyl; piperidine-3-yl; 1-acetyl-piperidine-3-yl; pyridin-2-yl; pyridin-3-yl; pyridin-4-yl; 6-oxo-1,6-dihydropyridin-2-yl; tetrahydrofuran-2-yl; tetrahydro-2H-pyran-2-yl; tetrahydro-2H-pyran-3-yl; tetrahydro-2H-pyran-4-yl; 1,2,3,4-tetrahydronaphth-1-yl; 1,2,3,4-tetrahydronaphth-2-yl; thiazol-5-yl; and thiazol-2-yl.

3. The method of claim 1 , wherein the compound has a structure according to the formula:

or a pharmaceutically acceptable salt thereof.

4. The method of claim 3 , wherein R 3 is selected from the group consisting of cyclohexyl; 1-methylcyclohexyl; 1-methoxycyclohexyl; cyclopentyl; morpholin-2-yl; 4-acetylmorpholin-2-yl; phenyl; 2-trifluoromethylphenyl; 3-azidophenyl; piperidine-3-yl; 1-acetyl-piperidine-3-yl; pyridin-2-yl; pyridin-3-yl; pyridin-4-yl; 6-oxo-1,6-dihydropyridin-2-yl; tetrahydrofuran-2-yl; tetrahydro-2H-pyran-2-yl; tetrahydro-2H-pyran-3-yl; tetrahydro-2H-pyran-4-yl; 1,2,3,4-tetrahydronaphth-1-yl; 1,2,3,4-tetrahydronaphth-2-yl; thiazol-5-yl; and thiazol-2-yl.

5. The method of claim 1 , wherein the compound is selected from the group consisting of

and pharmaceutically acceptable salts thereof.

6. The method of claim 1 , wherein the compound is selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

7. The method of claim 1 , wherein Z is selected from the group consisting of pyridin-2-yl-carbonyl and thiazol-2-yl-carbonyl.

8. The method of claim 7 , wherein the compound is selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

9. The method of claim 7 , wherein the compound is selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

10. The method of claim 1 , wherein the compound is administered as a pharmaceutical composition comprising the compound and a pharmaceutically acceptable excipient.

11. The method of claim 1 , wherein the compound is administered to the subject for at least one month.

12. The method of claim 1 , wherein the subject is a human, a canine, or a feline.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2023
From: QUINCE THERAPEUTICS, INC.
To: LIGHTHOUSE PHARMACEUTICALS, INC.
Reel/Frame 063468/0206 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2022
From: KONRADI, ANDREI W.; DOMINY, STEPHEN S.; LYNCH, CASEY CRAWFORD; COBURN, CRAIG; VACCA, JOSEPH
To: CORTEXYME, INC.
Reel/Frame 061305/0421 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2022
From: COBURN, CRAIG; VACCA, JOSEPH
To: WUXI APPTEC (SHANGHAI) CO., LTD.
Reel/Frame 061305/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2022
From: WUXI APPTEC (SHANGHAI) CO., LTD.
To: WUXI APPTEC (HONG KONG) LIMITED
Reel/Frame 061305/0801 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2022
From: WUXI APPTEC (HONG KONG) LIMITED
To: CORTEXYME, INC.
Reel/Frame 061305/0959 →
CHANGE OF NAME Recorded Oct 4, 2022
From: CORTEXYME, INC.
To: QUINCE THERAPEUTICS, INC.
Reel/Frame 061604/0790 →
Continuity (6)
Continuation 16399821 · Apr 30, 2019
Continuation 15996660 · Jun 4, 2018
Continuation 15683348 · Aug 22, 2017
Division 14875416 · Oct 5, 2015
Provisional Application 62060483 · Oct 6, 2014
Related Publication 20210017167A1 · Jan 21, 2021