IP Library Granted Patent US 11,180,521
Granted Patent B2
US 11,180,521 · App. 16/965,747 · Granted Nov 23, 2021

Nicotinamide riboside analogs, pharmaceutical compositions, and uses thereof

Inventors: Jonathan N. Kremsky (Arlington, MA); Bruce Szczepankiewicz (Hopkinton, MA); Hamish Toop (Sydney, AU); Jonathan Morris (Sydney, AU)
Assignees: Metro International Biotech, LLC; NewSouth Innovations Pty Ltd
C07H19/048
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Quick Facts
Patent No.
US 11,180,521
App. No.
16/965,747
Granted
Nov 23, 2021
Kind
B2
Abstract

Provided herein are compounds of Formula (I) and their salts, and compositions comprising such compounds that are useful for increasing the amount of NAD + in cells. Also disclosed are methods of using the disclosed compounds and compositions for treating, for example, diseases or disorders related to aging or stress, diabetes, obesity, mitochondrial diseases, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing.

Claims (34)

1. A compound having a structure of Formula (I):

or a pharmaceutically acceptable salt thereof, wherein:

B and B′ are each, independently

X − is a counteranion;

R 1 , R 2 , R 3 , R 1′ , R 2′ , and R 3′ are each independently hydrogen, substituted or unsubstituted alkyl, or substituted or unsubstituted —C(O)-alkyl;

R 4 is C 1 -C 6 -alkylene, C 2 -C 6 -alkenylene, C 2 -C 6 -alkynylene, C 3 -C 6 -cycloalkylene, C 3 -C 6 -cycloalkenylene, arylene, heterocyclylene, heteroarylene, or heteroaryl-C 2 -C 6 -alkylene, each of which is unsubstituted or substituted with one or more substituents selected from halo, OH, NO 2 , CN, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, —C(O)—C 1 -C 4 -alkyl, —C(O)-aryl, —C(O)-heteroaryl, —OC(O)—C 1 -C 4 -alkyl, —OC(O)-aryl, —OC(O)-heteroaryl, —NR a C(O)—C 1 -C 4 -alkyl, —NR a C(O)-aryl, —NR a C(O)-heteroaryl, aryl, and heteroaryl; and

R a is hydrogen or alkyl.

2. The compound of claim 1 , wherein the compound has a structure of Formula (II):

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 , wherein the compound has a structure of Formula (III):

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein the compound has a structure of Formula (IV):

or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 , wherein the compound has a structure of Formula (V):

or a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 , wherein R 4 is a moiety of structural formula:

wherein R 5 is hydrogen, halo, OH, NO 2 , CN, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, —C(O)—C 1 -C 4 -alkyl, —C(O)-aryl, —C(O)-heteroaryl, —OC(O)—C 1 -C 4 -alkyl, —OC(O)-aryl, —OC(O)-heteroaryl, —NR a C(O)—C 1 -C 4 -alkyl, —NR a C(O)-aryl, —NR a C(O)-heteroaryl, aryl, or heteroaryl; and

m and n are each integers from 1 to about 6, wherein the value of m is independent of the value of n.

7. The compound of claim 1 , wherein R 4 is selected from:

8. The compound of claim 1 , wherein R 4 is heterocycloalkylene selected from monosaccharides, disaccharides, oligosaccharides, and polysaccharides, where the oxygen atoms attached to R 4 are oxygen atoms of the monosaccharide, disaccharide, oligosaccharide, or polysaccharide in its unbound form.

9. The compound of claim 1 , wherein each X − is independently selected from Cl − , OH − , SO 4 H − , HPO 4 2− , CH 3 COO − , CF 3 COO − , PF 6 − , CH 3 SO 3 − , CF 3 SO 3 − , and PhCO 2 − .

10. The compound of claim 1 , wherein each X − is CF 3 SO 3 − .

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

or a pharmaceutically acceptable salt thereof.

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

or a pharmaceutically acceptable salt thereof.

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

or a pharmaceutically acceptable salt thereof.

14. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient.

15. A method for promoting survival of a eukaryotic cell, comprising contacting the cell with a compound of claim 1 or a pharmaceutically acceptable salt thereof.

16. A method for treating insulin resistance, a metabolic syndrome, hypercholesterolemia, atherogenic dyslipidemia, diabetes, or complications thereof, or for increasing insulin sensitivity in a subject, comprising administering to a subject in need thereof a compound of claim 1 or a pharmaceutically acceptable salt thereof.

17. A method for treating a neurological or neurodegenerative disorder in a subject, comprising administering to a subject in need thereof of a compound according to claim 1 or a pharmaceutically acceptable salt thereof.

18. The method of claim 16 , wherein the subject is human.

19. The method of claim 17 , wherein the subject is human.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2024
From: NEWSOUTH INNOVATIONS PTY LTD
To: METRO BIOTECH NSW PTY LTD
Reel/Frame 066669/0529 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2024
From: METRO BIOTECH NSW PTY LTD
To: METRO INTERNATIONAL BIOTECH, LLC
Reel/Frame 066670/0305 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2021
From: KREMSKY, JONATHAN N.; SZCZEPANKIEWICZ, BRUCE
To: METRO INTERNATIONAL BIOTECH, LLC
Reel/Frame 054963/0156 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2021
From: TOOP, HAMISH; MORRIS, JONATHAN
To: NEWSOUTH INNOVATIONS PTY LTD
Reel/Frame 054963/0202 →
Continuity (2)
Provisional Application 62623579 · Jan 30, 2018
Related Publication 20210032280A1 · Feb 4, 2021
Cited By (3)
US 12,391,721 US 12,485,135 US 12,616,713