IP Library Granted Patent US 7,504,384
Granted Patent B2
US 7,504,384 · App. 11/220,965 · Granted Mar 17, 2009

Use of lipid conjugates in the treatment of infection

Assignee: Yissum Research Development Company of the Hebrew University of Jerusalem
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Quick Facts
Patent No.
US 7,504,384
App. No.
11/220,965
Granted
Mar 17, 2009
Kind
B2
Abstract

This invention provides compounds and methods of use thereof in suppressing, inhibiting, preventing, or treating a pathogenic effect on a cell, including, inter alia, infection with intracellular pathogens. Also provided are compounds and methods of use thereof in suppressing, inhibiting, preventing, or treating an infection in a subject.

Claims (19)

1. A method of suppressing, inhibiting, or treating an infection in a subject comprising the step of administering to said subject an effective amount of a lipid conjugate compound, or its pharmaceutically acceptable salt or pharmaceutical product thereof, wherein said compound is represented by the structure of the general formula (I):

wherein

R 1 is a linear, saturated, mono-unsaturated, or poly-unsaturated, alkyl chain ranging in length from 2 to 30 carbon atoms;

R 2 is a linear, saturated, mono-unsaturated, or poly-unsaturated, alkyl chain ranging in length from 2 to 30 carbon atoms;

Y is either nothing or a spacer group ranging in length from 2 to 30 atoms;

X is either a physiologically acceptable monomer, dimer, oligomer or a physiologically acceptable polymer, wherein X is a glycosaminoglycan; and

n is a number from 1 to 1,000;

wherein if Y is nothing the phosphatidylethanolamine is directly linked to X via an amide bond and if Y is a spacer, said spacer is directly linked to X via an amide or an esteric bond and to said phosphatidylethanolamine via an amide bond.

2. The method according to claim 1 , wherein said R 1 and R 2 are myristic acid moieties.

3. The method according to claim 1 , wherein said glycosaminoglycan is chondroitin sulfate.

4. The method according to claim 3 , wherein said chondroitin sulfate is chondroitin-6-sulfate, chondroitin-4-sulfate or a derivative thereof.

5. The method according to claim 1 , wherein said glycosaminoglycan is heparin.

6. The method according to claim 1 , wherein said physiologically acceptable polymer is hyaluronic acid.

7. The method according to claim 1 , wherein said infection is viral.

8. The method according to claim 7 , wherein said infection is mediated by influenza virus.

9. The method according to claim 7 , wherein said infection is mediated by Human Immunodeficiency Virus (HIV).

10. The method according to claim 7 , wherein said infection is mediated by a poxvirus.

11. The method according to claim 1 , wherein said infection is bacterial.

12. The method according to claim 11 , wherein said infection is mediated by Chlamydia.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2018
From: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM, LTD
To: YEDGAR, SAUL
Reel/Frame 046006/0942 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2006
From: YEDGAR, MR. SAUL; OJCIUS, MR. DAVID
To: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM
Reel/Frame 017043/0866 →
Continuity (6)
Continuation In Part 1095249600 · Sep 29, 2004
Continuation In Part 1062798100 · Jul 28, 2003
Continuation In Part 0975676500 · Jan 10, 2001
Provisional Application 6017490500 · Jan 10, 2000
Provisional Application 6017490700 · Jan 10, 2000
Related Publication 20060079485A1 · Apr 13, 2006