David W Boykin

US Patent:

6423737, Jul 23, 2002

Filed:

Jan 12, 2001

Appl. No.:

09/759664

Inventors:

James E. Hall - Chapel Hill NC
Richard R. Tidwell - Pittsboro NC
David W. Boykin - Atlanta GA

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA

International Classification:

A61K 3115

US Classification:

514399, 514438, 514471, 514633

Abstract:

A method of treating pneumonia in a subject in need of such treatment is disclosed. The method comprises orally administering to the subject a bis-benzamidoxime, or a pharmaceutically acceptable salt thereof, that is reduced in the subject to produce a benzamidine having anti- activity. The method of the present invention may alternatively comprise intravenously administering to the subject an active compound as disclosed herein. Pharmaceutical formulations and active compounds useful in the practice of the present invention are also disclosed.

US Patent:

6486200, Nov 26, 2002

Filed:

Jul 7, 2000

Appl. No.:

09/612138

Inventors:

David W. Boykin - Atlanta GA
M. Syed Rahmathullah - Mississauga, CA
Richard R. Tidwell - Pittsboro NC
James E. Hall - Chapel Hill NC

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA

International Classification:

A61K 31357

US Classification:

514467, 514473, 549448, 549450, 549451

Abstract:

A methods of treating an infection comprises administering a therapeutically effective amount of a compound described by the Formula (I): wherein: X may be O, S, or NRâ wherein Râ is H or loweralkyl; R and R may be independently selected from the group consisting of H, loweralkyl, oxyalkyl, alkoxyalkyl, cycloalkyl, aryl, hydroxyalkyl, aminoalkyl, and alkylaminoalkyl; R and R are each independently selected from the group consisting of H, loweralkyl, halogen, oxyalkyl, oxyaryl, and oxyarylalkyl; R is represented by a formula selected from the group consisting of: âwherein: X , X , and X are independently selected from O and S; and R and R are independently selected from the group consisting of loweralkyl, aryl, alkylaryl, oxyaryl, an ester-containing substituent, and oxyalkyl; or a pharmaceutically acceptable salt thereof.

US Patent:

6503940, Jan 7, 2003

Filed:

Jul 31, 2001

Appl. No.:

09/918787

Inventors:

David W. Boykin - Atlanta GA
M. Syed Rahmathullah - Mississauga, CA
Richard R. Tidwell - Pittsboro NC
James E. Hall - Chapel Hill NC

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA

International Classification:

A61K 3140

US Classification:

514422, 548541, 548556, 549448, 549449, 549450, 549451, 514423

Abstract:

A methods of treating an infection comprises administering a therapeutically effective amount of a compound described by the Formula (I): wherein: X may be O, S, or NRâ wherein Râ is H or loweralkyl, R and R may be independently selected from the group consisting of H, loweralkyl, oxyalkyl, alkoxyalkyl, cycloalkyl, aryl, hydroxyalkyl, aminoalkyl, and alkylaminoalkyl; R and R are each independently selected from the group consisting of H, loweralkyl, halogen, oxyalkyl, oxyaryl, and oxyarylalkyl; R is represented by a formula selected from the group consisting of: wherein: X , X , and X are independently selected from O and S; and R and R are independently selected from the group consisting of loweralkyl, aryl, alkylaryl, oxyaryl, an ester-containing substituent, and oxyalkyl; or a pharmaceutically acceptable salt thereof.

US Patent:

6613787, Sep 2, 2003

Filed:

Dec 20, 2000

Appl. No.:

09/745004

Inventors:

W. David Wilson - Atlanta GA
David W. Boykin - Atlanta GA
Richard R. Tidwell - Pittsboro NC

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA

International Classification:

A61K 31415

US Classification:

514394, 5483047, 549472

Abstract:

Asymmetric derivatives of furamidines with one of the phenyl rings of furamidine replaced with a benzimidazole have been found by quantitative footprinting analyses to bind GC containing sites on DNA more strongly than to pure AT sequences. These compounds have been shown to bind in the minor groove at specific GC containing sequences of DNA in a highly cooperative manner as a stacked dimer. Compounds of the present invention find use in selectively binding mixed sequence DNA, and may also be used in methods of regulating gene expression, methods of treating opportunistic infections and cancer, as well as in methods of detecting certain sequences of DNA.

US Patent:

6649652, Nov 18, 2003

Filed:

Jul 30, 2002

Appl. No.:

10/208947

Inventors:

David W. Boykin - Atlanta GA
M. Syed Rahmathullah - Mississauga, CA
Richard R. Tidwell - Pittsboro NC
James E. Hall - Chapel Hill NC

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA

International Classification:

C07D31704

US Classification:

514467, 514473, 549229, 549448, 549449, 549451

Abstract:

A methods of treating an infection comprises administering a therapeutically effective amount of a compound described by the Formula (I).

US Patent:

6706754, Mar 16, 2004

Filed:

Nov 5, 2001

Appl. No.:

09/985590

Inventors:

Karl A. Werbovetz - Worthington OH
James J. Brendle - Beltsville MD
David W. Boykin - Atlanta GA
Chad E. Stephens - Villa Rica GA

Assignee:

The United States of America as represented by the Secretary of the Army - Washington DC

International Classification:

A61K 3138

US Classification:

514438, 514461, 514631, 514634

Abstract:

Methods for treating, preventing or inhibiting leishmaniasis in a subject comprising administering to the subject a therapeutically effective amount of at least one compound having the structural formula wherein Y is a heteroatom; R and R are independently H or an alkyl, cycloalkyl, heterocycloalkyl, aryl, amino or heteroaryl group; and X , X , and X are independently H or an alkyl, alkoxy, halo, amino, alkylamino, dialkylamino, acylamino, alkylthio, sulfonyl, cyano, carboxy, alkoxycarbonyl, or carbamoyl group are disclosed.

US Patent:

6737440, May 18, 2004

Filed:

Nov 6, 2001

Appl. No.:

10/008535

Inventors:

David W. Boykin - Atlanta GA
Richard R. Tidwell - Pittsboro NC
W. David Wilson - Atlanta GA
John R. Perfect - Durham NC
Chad F. Stephens - Villa Rica GA

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA
Duke University - Durham NC

International Classification:

A61K 3127

US Classification:

514491, 514472, 549491, 549472

Abstract:

The present invention relates to novel 2,5-bis {[alkyl(or aryl)imino]aminophenyl}furans and thiophenes of the general formula in which R , R , R and R are each independently selected from the group consisting of H, alkyl, alkoxy, halide, and alkylhalide groups; R is H, alkyl or aryl; R is H, alkyl, aryl, or NR R , in which R and R are each independently selected from the group consisting of H, alkyl and aryl; and X is O, S or NR , in which R is H or alkyl, and to the use of such compounds.

US Patent:

6774144, Aug 10, 2004

Filed:

Nov 1, 2000

Appl. No.:

09/703804

Inventors:

Christine C. Dykstra - Auburn AL
James C. Hudson - Carpenteria CA
Sandra Ewald - Auburn AL
Richard R. Tidwell - Pittsboro NC
David W. Boykin - Atlanta GA

Assignee:

The University of North Carolina at Chapel Hill - Chapel Hill NC
Georgia State University Research Foundation, Inc. - Atlanta GA
Auburn University - Auburn AL

International Classification:

A61K 3134

US Classification:

514461, 514472, 514473

Abstract:

In one aspect, the invention relates to a method of treating infectious bursal disease (IBD) in an avian subject in need of such treatment. The method comprises administering to the subject a compound of the formulas (I) through (IV) or a pharmaceutically acceptable salt thereof in an amount sufficient to treat IBD. In another aspect, the invention relates to a method of producing active immunity against infectious bursal virus disease (IBD) in an avian subject. The method comprises administering to a subject an immunogenic-amount of an IBDV vaccine and a compound selected from the compounds of formulas (I) through (IV) described herein. The compound represented by formulas (I) through (IV) is administered in an amount sufficient to induce an immune response in the avian subject.