IP Library Granted Patent US 8,563,580
Granted Patent B2
US 8,563,580 · App. 13/120,583 · Granted Oct 22, 2013

Patent

Inventors: Radhakrishnan Padmanabhan (Bethesda, MD); Nagarajan Pattabiraman (North Potomac, MD); Niklaus Mueller (Denver, CO); Kuppuswamy Nagarajan (Bangalore, IN)
Assignee: Georgetown University
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Quick Facts
Patent No.
US 8,563,580
App. No.
13/120,583
Granted
Oct 22, 2013
Kind
B2
Abstract

Methods of treating, preventing, and/or ameliorating a Flavivirus infection in a subject are disclosed. The methods comprise administering to the subject a therapeutically effective amount of a Flavivirus inhibitor, e.g., a Flavivirus serine protease inhibitor. These methods are useful in treating, preventing, and/or ameliorating Flavivurs infections such as, for example, West Nile Virus, Dengue Virus, and Japanese Encephalitis Virus.

Claims (15)

1. A method of treating a Flavivirus infection in a subject, comprising administering to the subject a therapeutically effective amount of a compound of the following formula:

or a pharmaceutically acceptable salt or prodrug thereof, wherein:

R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are each independently selected from hydrogen, hydroxyl, substituted or unsubstituted C 1-4 alkyl, substituted or unsubstituted C 1-4 heteroalkyl, substituted or unsubstituted C 2-4 alkenyl, substituted or unsubstituted C 2-4 heteroalkenyl, substituted or unsubstituted C 2-4 alkynyl, substituted or unsubstituted C 2-4 heteroalkynyl, or halogen;

A is selected from the group consisting of:

B is selected from hydrogen, substituted or unsubstituted C 1-12 alkyl, substituted or unsubstituted C 1-12 heteroalkyl, substituted or unsubstituted C 2-12 alkenyl, substituted or unsubstituted C 2-12 heteroalkenyl, substituted or unsubstituted C 2-12 alkynyl, substituted or unsubstituted C 2-12 heteroalkynyl, substituted or unsubstituted aryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted arylalkyl, substituted or unsubstituted heteroarylalkyl, substituted or unsubstituted cycloalkylalkyl, and substituted or unsubstituted heterocycloalkylalkyl; and

R 7 is hydrogen or an attachment for a cyclic B group,

with the proviso that R 1 is not OH if

A is

and B is

2. The method of claim 1 , wherein the Flavivirus is the West Nile Virus.

3. The method of claim 1 , wherein the Flavivirus is Dengue Virus serotype DEN-1, Dengue Virus serotype DEN-2, Dengue Virus serotype DEN-3, or Dengue Virus serotype DEN-4.

4. The method of claim 1 , wherein the Flavivirus is Japanese Encephalitis Virus.

5. The method of claim 1 , wherein the compound is selected from the group consisting of:

6. A method of treating a Flavivirus infection in a subject, comprising administering to the subject a therapeutically effective amount of a compound of the following structure:

or a pharmaceutically acceptable salt or prodrug thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2012
From: PADMANABHAN, RADHAKRISHNAN; PATTABIRAMAN, NAGARAJAN; MUELLER, NIKLAUS; NAGARAJAN, KUPPUSWAMY
To: GEORGETOWN UNIVERSITY
Reel/Frame 027935/0277 →
Continuity (2)
Provisional Application 61099411 · Sep 23, 2008
Related Publication 20110224207A1 · Sep 15, 2011