IP Library Granted Patent US 8,969,342
Granted Patent B2
US 8,969,342 · App. 13/257,418 · Granted Mar 3, 2015

Compounds and methods for treating mammalian gastrointestinal microbial infections

Inventors: Lizbeth K. Hedstrom (Newton, MA); Gregory D. Cuny (Houston, TX); Deviprasad R. Gollapalli (Waltham, MA); Boris Striepen (Athens, GA); Suresh Kumar Gorla (Waltham, MA); Mandapati Kavitha (Waltham, MA)
Assignees: Brandeis University; University of Georgia Research Foundation, Inc.; The Brigham and Women's Hospital, Inc.
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Quick Facts
Patent No.
US 8,969,342
App. No.
13/257,418
Granted
Mar 3, 2015
Kind
B2
Abstract

Described herein are compounds, and pharmaceutically acceptable salts and prodrugs thereof, which are useful as inhibitors of IMPDH. In certain embodiments, a compound of the invention selectively inhibits a parasitic IMPDH versus a host IMPDH. Further, the invention provides pharmaceutical compositions comprising one or more compounds of the invention. The invention also relates to methods of treating various parasitic and bacterial infections in mammals. Moreover, the compounds may be used alone or in combination with other therapeutic or prophylactic agents, such as anti-virals, anti-inflammatory agents, antimicrobials and immunosuppressants.

Claims (25)

1. A compound, or a pharmaceutically acceptable salt thereof, represented by Formula XII:

wherein, independently for each occurrence,

m is 0, 1, or 2;

R 2 is hydrogen or alkyl;

p is 0, 1, 2, or 3;

q is 0, 1, 2, 3, or 4; and

R 5 is halo, azido, alkyl, haloalkyl, hydroxyalkyl, aminoalkyl, heterocycloalkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, heteroaralkyl, hydroxy, alkoxy, haloalkyloxy, aryloxy, heteroaryloxy, amino, nitro, sulfhydryl, imino, amido, phosphonate, phosphinate, acyl, carboxyl, alkoxycarbonyl, carboxylic acid, acyloxy, alkylthio, sulfonate, sulfonyl, sulfonamido, formyl, cyano, oxime, or isocyano.

2. The compound of claim 1 , wherein m is 1.

3. The compound of claim 1 , wherein m is 1; and R 2 is alkyl.

4. The compound of claim 1 , wherein

5. The compound of claim 1 , wherein

6. A compound selected from the group consisting of:

7. A method of killing or inhibiting the growth of a microbe, comprising the step of contacting said microbe with an effective amount of a compound of claim 1 .

8. The method of claim 7 , wherein said microbe is a protozoon, a bacterium, or a fungus.

9. The method of claim 7 , wherein said microbe is a protozoon or a bacterium selected from the group consisting of the genera Eimeria, Cryptosporidium, Babesia, Theileria, Neospora, Sarcocystis, Giardia, Entamoeba, Trichomonas, Tritrichomonas, Leishmania, Trypanosoma, Helicobacter, Borrelia, Streptococcus, Campylobacter, Arcobacter, Bacteroides, Fusobacterium, Burkholderia, Clostridia, Neisseria, Mycobacterium , and Acinetobacter.

10. The method of claim 8 , wherein said microbe is a protozoon; and said protozoon is selected from the group consisting of the genera Eimeria, Cryptosporidium, Babesia, Theileria, Neospora, Sarcocystis, Giardia, Entamoeba, Trichomonas, Tritrichomonas, Leishmania and Trypanosoma.

11. The method of claim 8 , wherein said microbe is a bacterium; and said bacterium is selected from the group consisting of the genera Helicobacter, Borrelia, Streptococcus, Campylobacter, Arcobacter, Bacteroides, Fusobacterium, Burkholderia, Clostridia, Neisseria, Mycobacterium , and Acinetobacter.

12. A method of treating or preventing a microbial infection in a mammal comprising the step of administering to a mammal in need thereof a therapeutically effective amount of a compound of claim 1 .

13. The method of claim 12 , wherein said microbial infection is caused by a protozoon, a bacterium, or a fungus.

14. The method of claim 12 , wherein said microbial infection is caused by a protozoon or a bacterium selected from the group consisting of the genera Eimeria, Cryptosporidium, Babesia, Theileria, Neospora, Sarcocystis, Giardia, Entamoeba, Trichomonas, Leishmania, Trypanosoma, Helicobacter, Borrelia, Streptococcus, Campylobacter, Arcobacter, Bacteroides, Fusobacterium, Burkholderia, Clostridia, Neisseria, Mycobacterium , and Acinetobacter.

15. The method of claim 13 , wherein said microbial infection is caused by a protozoon; and said protozoon is selected from the group consisting of the genera Eimeria, Cryptosporidium, Babesia, Theileria, Neospora, Sarcocystis, Giardia, Entamoeba, Trichomonas, Tritrichomonas, Leishmania and Trypanosoma.

16. The method of claim 12 , wherein said microbial infection is caused by a bacterium; and said bacterium is selected from the group consisting of the genera Helicobacter, Borrelia, Streptococcus, Campylobacter, Arcobacter, Bacteroides, Fusobacterium, Burkholderia, Clostridia, Neisseria, Mycobacterium , and Acinetobacter.

17. The method of claim 10 , wherein the protozoon is of the genera Cryptosporidium.

18. The method of claim 15 , wherein the protozoon is of the genera Cryptosporidium.

19. The method of claim 12 , wherein said microbial infection is caused by a bacterium; and said bacterium is selected from the group consisting of the genera Bacillus and Staphylococcus .

Assignments (4)
CONFIRMATORY LICENSE Recorded Dec 15, 2017
From: BRANDEIS UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044882/0350 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2011
From: STRIEPEN, BORIS
To: UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC.
Reel/Frame 027433/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2011
From: CUNY, GREGORY D.
To: THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
Reel/Frame 027433/0363 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2011
From: HEDSTROM, LIZBETH K.; GOLLAPALLI, DEVIPRASAD R.; KIRUBAKARAN, SIVAPRIYA; MAURYA, SUSHIL KUMAR; GORLA, SURESH KUMAR; JOHNSON, COREY ROBERT; KAVITHA, MANDAPATI; KHAN, JIHAN
To: BRANDEIS UNIVERSITY
Reel/Frame 027433/0377 →
Continuity (2)
Provisional Application 61162013 · Mar 20, 2009
Related Publication 20120101096A1 · Apr 26, 2012