IP Library Granted Patent US 10,730,826
Granted Patent B2
US 10,730,826 · App. 16/353,786 · Granted Aug 4, 2020

Ketone inhibitors of lysine gingipain

Inventors: Andrei W. Konradi (Burlingame, CA); Robert A. Galemmo, Jr. (South San Francisco, CA); Stephen S. Dominy (Novato, CA); Casey C. Lynch (San Francisco, CA); Leslie J. Holsinger (Los Altos, CA)
Assignee: CORTEXYME, INC.
C07C233/62A61K31/165A61K31/167A61K31/41A61K31/42A61K31/44A61K31/4402A61K31/4406A61K31/4409A61K31/4439A61K31/505A61K31/513A61K31/655A61K45/06A61P25/00A61P31/04C07B59/001C07C233/78C07C235/10C07C235/50C07C237/42C07C245/08C07C247/16C07C247/18C07C317/28C07C323/40C07C323/42C07C381/00C07D213/65C07D213/68C07D213/70C07D213/81C07D213/82C07D239/34C07D239/36C07D239/38C07D257/04C07D261/12C07D401/12C07D413/12C07F5/02C07C2601/08
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,730,826
App. No.
16/353,786
Granted
Aug 4, 2020
Kind
B2
Abstract

The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis . Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.

Claims (24)

1. A compound according to Formula I:

or a pharmaceutically acceptable salt thereof, wherein:

A is —CH 2 —;

R 1a , R 1b , R 2a , R 2b , and R 4 are hydrogen;

R 3 is selected from the group consisting of C 3-8 cycloalkyl, C 3-8 alkyl,

3- to 12-membered heterocyclyl, C 6-10 aryl, and 5- to 12-membered heteroaryl, wherein R 3 is optionally substituted with one or more R 3a substituents;

each R 3a is independently selected from the group consisting of halogen, —N 3 , C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxy, C 1-4 haloalkoxy, —N(R c ) 2 , —N + (R b ) 3 , and —NR c C(O)R b ;

each R b is independently selected from the group consisting of C 1-4 alkyl, C 1-4 haloalkyl, and C 1-4 deuteroalkyl;

each R c is independently selected from the group consisting of hydrogen and C 1-8 alkyl;

R 5 is —CH 2 R 5a ; and

R 5a is —O-phenyl, wherein phenyl is substituted with 1-5 halogens;

provided that R 5 is other than 2,3,5, 6-tetrafluorophenoxymethyl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, having a structure according to Formula Ia:

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is C 3-8 cycloalkyl.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 5a is selected from the group consisting of 2,3,6-trifluorophenoxy; 2,3,5-trifluorophenoxy; 2,3,4-trifluorophenoxy; 3,4,5-trifluorophenoxy; 2,3-difluorophenoxy; 2,4-difluorophenoxy; 2,5-difluorophenoxy; 2,6-difluorophenoxy; 3,4-difluorophenoxy; 3,5-difluorophenoxy; 2-fluorophenoxy; 3-fluorophenoxy; and 4-fluorophenoxy.

5. The compound of claim 3 , or a pharmaceutically acceptable salt thereof, wherein R 5a is selected from the group consisting of 2,3,6-trifluorophenoxy; 2,3,5-trifluorophenoxy; 2,3,4-trifluorophenoxy; 3,4,5-trifluorophenoxy; 2,3-difluorophenoxy; 2,4-difluorophenoxy; 2,5-difluorophenoxy; 2,6-difluorophenoxy; 3,4-difluorophenoxy; 3,5-difluorophenoxy; 2-fluorophenoxy; 3-fluorophenoxy; and 4-fluorophenoxy.

6. The compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein R 5a is selected from the group consisting of 2,3,6-trifluorophenoxy; 2,3,5-trifluorophenoxy; 2,3,4-trifluorophenoxy; and 3,4,5-trifluorophenoxy.

7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of:

8. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of:

9. The compound of claim 1 , which is

or a pharmaceutically acceptable salt thereof.

10. The compound of claim 1 , which is

or a pharmaceutically acceptable salt thereof.

11. A pharmaceutical composition comprising according to any one of the preceding claims, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2023
From: QUINCE THERAPEUTICS, INC.
To: LIGHTHOUSE PHARMACEUTICALS, INC.
Reel/Frame 063468/0206 →
CHANGE OF NAME Recorded Aug 17, 2022
From: CORTEXYME, INC.
To: QUINCE THERAPEUTICS, INC.
Reel/Frame 061204/0338 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2019
From: KONRADI, ANDREI W.; GALEMMO, ROBERT A., JR.; DOMINY, STEPHEN S.; LYNCH, CASEY C.; HOLSINGER, LESLIE J.
To: CORTEXYME, INC.
Reel/Frame 049204/0213 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2019
From: GALEMMO, ROBERT A., JR.
To: WUXI APPTEC (SHANGHAI) CO., LTD.
Reel/Frame 049204/0244 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2019
From: WUXI APPTEC (SHANGHAI) CO., LTD.
To: WUXI APPTEC (HONG KONG) LIMITED
Reel/Frame 049204/0314 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2019
From: WUXI APPTEC (HONG KONG) LIMITED
To: CORTEXYME, INC.
Reel/Frame 049204/0374 →
Continuity (4)
Continuation PCTUS2017051912 · Sep 15, 2017
Provisional Application 62459456 · Feb 15, 2017
Provisional Application 62395938 · Sep 16, 2016
Related Publication 20190210960A1 · Jul 11, 2019
Cited By (1)
US 12,318,377