TLR4 inhibitors for the treatment of human infectious and inflammatory disorders

Patent metadata

Field	Value
Publication number	US-9072760-B2
Application number	US-201313848809-A
Country	US
Kind code	B2
Filing date	Mar 22, 2013
Priority date	Sep 24, 2010
Publication date	Jul 7, 2015
Grant date	Jul 7, 2015

Abstract

The present invention relates to methods of treating infectious, inflammatory and post-traumatic disorders by administering various compounds newly discovered to have TLR4 inhibitory activity. In addition to methods of treatment, the present invention further provides for pharmaceutical compositions comprising said compounds, together with a suitable pharmaceutical carrier. Because TLR4 is the most upstream receptor in the pro-inflammatory LPS signaling cascade, treatments of the invention, which inhibit or antagonize TLR4 action, may avoid the pitfalls associated with other cytokine inhibitors that act further down the pathway and accordingly play a less specific (and perhaps non-critical) role.

First claim

We claim:

1. A method of treating an infectious or inflammatory disorder comprising administering, to a subject in need of such treatment, an effective amount of a Toll-like receptor 4 inhibitor compound selected from the compounds listed in TABLE 1 that reduces one or more sign or symptom of inflammation in the subject.

2. The method of claim 1 where the subject is suffering from sepsis.

3. The method of claim 1 where the subject is suffering from arthritis.

4. The method of claim 1 , where the Toll-like receptor 4 inhibitor compound is selected from the group consisting of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside, 2-(acetylamino)-2-deoxy-D-galactopyranose hydrate, and 2-(acetylamino)-2-deoxy-4-O-hexopyranosylhexopyranose.

5. The method of claim 1 , where the Toll-like receptor 4 inhibitor is a derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside.

6. A method of treating an intestinal inflammatory disorder in a subject comprising administering, to a subject in need of such treatment, an effective amount of a T4IC selected from the compounds listed in TABLE 1 that reduces intestinal inflammation in the subject.

7. The method of claim 6 where the subject is suffering from necrotizing enterocolitis.

8. The method of claim 6 where the subject is suffering from ulcerative colitis.

9. The method of claim 6 where the subject is suffering from Crohn's disease.

10. The method of claim 6 , where the Toll-like receptor 4 inhibitor compound is selected from the group consisting of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside, 2-(acetylamino)-2-deoxy-D-galactopyranose hydrate, and 2-(acetylamino)-2-deoxy-4-O-hexopyranosylhexopyranose.

11. The method of claim 6 , where the Toll-like receptor 4 inhibitor is a derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside.

12. A method of treating a cardiovascular disease in a subject comprising administering, to a subject in need of such treatment, an effective amount of a Toll-like receptor 4 inhibitor compound selected from the compounds listed in TABLE 1 that reduces myocardial ischemia in the subject.

13. The method of claim 12 , where the subject is suffering from angina.

14. The method of claim 12 , where the subject has suffered a myocardial infarction.

15. The method of claim 12 , where the subject is at increased risk of suffering a myocardial infarction.

16. The method of claim 12 , where the Toll-like receptor 4 inhibitor compound is selected from the group consisting of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside, 2-(acetylamino)-2-deoxy-D-galactopyranose hydrate, and 2-(acetylamino)-2-deoxy-4-O-hexopyranosylhexopyranose.

17. The method of claim 12 , where the Toll-like receptor 4 inhibitor is a derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside.

18. A method of treating a traumatic injury in a subject comprising administering, to a subject in need of such treatment, an effective amount of a Toll-like receptor 4 inhibitor compound selected from the compounds listed in TABLE 1 that reduces Toll-like receptor 4-induced post-traumatic injury.

19. The method of claim 18 , where the traumatic injury is to an organ selected from the group consisting of the heart, the liver, the lung, the kidney, the intestine, the brain, the eye and the pancreas.

20. The method of claim 18 , where the Toll-like receptor 4 inhibitor compound is selected from the group consisting of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside, 2-(acetylamino)-2-deoxy-D-galactopyranose hydrate, and 2-(acetylamino)-2-deoxy-4-O-hexopyranosylhexopyranose.

21. The method of claim 18 , where the Toll-like receptor 4 inhibitor is a derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside.

22. The method of claim 5 where the derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside is one of the following compounds:

23. The method of claim 11 where the derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside is one of the following compounds:

24. The method of claim 17 where the derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside is one of the following compounds:

25. The method of claim 21 where the derivative of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside is one of the following compounds:

26. A pharmaceutical composition comprising a therapeutically effective amount of a of isopropyl 3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxyhexopyranoside derivative selected from the group consisting of:

Assignees

• Univ Pittsburgh—Of The Commonwealth System Of Higher Education

Inventors

• Wipf Peter
• Neal Matthew D
• Chhinder Sodhi P
• Hackam David J

Classifications

• A61K31/351

  not condensed with another ring · CPC title

• A61K31/7024

  Esters of saccharides · CPC title

• A61K31/7008 Primary

  Compounds having an amino group directly attached to a carbon atom of the saccharide radical, e.g. D-galactosamine, ranimustine · CPC title

• A61K31/7028 Primary

  Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages · CPC title

• A61K31/7034

  attached to a carbocyclic compound, e.g. phloridzin · CPC title