Steven Lyman Wood
Burglar Alarm in Orem, UT

6686393, Feb 3, 2004

Sep 16, 1992

07/946813

Bronwyn G. Hughes - Orem UT
Steven G. Wood - Orem UT

Murdock International Corporation - Springville UT

A61K 31195

514561, 514680

The present invention is directed to the use of antiviral compounds having the following generalized structure: wherein R is 2H or O; R′ is OH, H, or COOH (single substitution); and R″ is OH, H, or alkyl; and pharmaceutically acceptable salts thereof as therapeutic substances having antiviral activity against human cytomegalovirus (“HCMV”) and for treating diseases caused by HCMV. Dimeric forms of the forgoing antiviral compounds having antiviral activity against HCMV are also disclosed. Pharmaceutical compositions containing the disclosed antiviral compounds are disclosed for topical and systemic administration.

6569891, May 27, 2003

May 2, 2002

09/979376

Noel L. Owen - Provo UT
Steven Glen Wood - Orem UT

Brigham Young University - Provo UT

A61K 31352

514453, 549381, 536 41, 514 25

A compound isolated from an aqueous leachate of heartwood of “Palo de Brazil” has antihypertensive activity. The compound was isolated by reversed-phase high pressure liquid chromatography to separate it from haematoxylin, which is co-extracted with the new compound. The compound is effective in reducing the blood pressure of hypertensive Sprague-Dawley rats.

4505929, Mar 19, 1985

Aug 16, 1982

6/408362

Lowell D. Markley - Midland MI
Yulan C. Tong - Walnut Creek CA
Steven G. Wood - Orem UT

The Dow Chemical Company - Midland MI

A01N 3734, C07C12150, C07C14378, C07C14374

514520

Novel compounds exhibiting antiviral activity are disclosed, such compounds are represented by the formula: ##STR1## wherein m represents the integer 0, 1 or 2; R represents trihalomethyl, alkyl or phenyl; R. sub. 1 represents hydrogen, bromo, chloro, fluoro, cyano, nitro, amino, alkyl, alkoxy or trifluoromethyl; R. sub. 2 represents hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH. sub. 2). sub. n R. sub. 4 wherein n represents the integer 1, 2 or 3 and R. sub. 4 represents cyano or dialkylamino; R. sub. 3 represents hydrogen, hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH. sub. 2). sub. n R. sub. 4 wherein n represents the integer 1, 2 or 3; and R. sub.

4865480, Sep 12, 1989

Jul 20, 1987

7/075523

Valdon G. Reynolds - Bountiful UT
Steven M. Wood - Orem UT
Joseph T. Sorenson - Salt Lake City UT

Sorenson Development Incorporated - Salt Lake City UT

B43K 2108, A61M 3500

401175

An applicator for dispensing metered amounts of medicaments in stick formulations is comprised of a hollow tube and a piston mounted to slidingly move within the tube. A finger operable base is rotatably mounted at one end of the tube and is mechanically linked by a screw member to the piston to urge the piston towards the other end of the tube. A depressible thumb piece is associated with the rotatable base. An extension or post is associated with the thumb piece to extend inward of the tube and to register with a race formed inside the tube. The race has a series of detents with which the extension may register upon rotation of the base. Registration between the extension and the detents signals certain increments of rotation or prevents further rotation of the base. The thumb piece is depressed inward to bring the extension out of registration with the detents. A medicated formulation is disposed within the tube such that the piston urges the formulation towards the other end of the tube to extend an incremental amount of the formulation beyond the open end of the tube to be applied directly to the user.

4349568, Sep 14, 1982

Jun 12, 1980

6/158964

Lowell D. Markley - Midland MI
Yulan C. Tong - Walnut Creek CA
Steven G. Wood - Orem UT

The Dow Chemical Company - Midland MI

A61K 31135, A61K 3110, C07C 43263

424330

Novel compounds exhibiting antiviral activity are disclosed, such compounds are represented by the formula: ##STR1## wherein m represents the integer 0, 1 or 2; R represents trihalomethyl, alkyl or phenyl; R. sub. 1 represents hydrogen, bromo, chloro, fluoro, cyano, nitro, amino, alkyl, alkoxy or trifluoromethyl; R. sub. 2 represents hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH. sub. 2). sub. n R. sub. 4 wherein n represents the integer 1, 2 or 3 and R. sub. 4 represents cyano or dialkylamino; R. sub. 3 represents hydrogen, hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH. sub. 2). sub. n R. sub. 4 wherein n represents the integer 1, 2 or 3; and R. sub.

2011007, Mar 24, 2011

Sep 24, 2010

12/890502

STEVEN G. WOOD - OREM UT, US
KATIE SOUTHWICK - AVENEL NJ, US
L. DEE NORD - OREM UT, US

A61K 39/00, C07H 15/06, A61K 31/739, A61K 38/19, A61P 35/00

4242771, 536 182, 514 25, 514 11

This disclosure provides, in certain embodiments, methods for generating and using extracts of (e.g., ) and/or epiphytic/endophytic bacteria associated therewith, either alone or in combination with conventional immunostimulant(s) or anti-inflammatory agents, for modulation of the immune system of a subject. Also provided are compositions that include specific extracts, bacteria isolated from tissue (in particular, species), and extracts of from such bacteria. Also provided herein are purified components of extracts and/or extracts from the epiphytic/endophytic bacteria, which extracts exhibit mitogenic or cytotoxic activities. Compositions provided herein can be used for the treatment of neutropenia subsequent to chemotherapy, and for the treatment of immune deficiency (e.g., such as is caused by toxic chemotherapy, disease, or advancing age), as well as in other immune-stimulatory methods. Other embodiments of the invention provide methods of producing extracts of the invention, as well as purified bioactive components thereof, including particularly bacterial LPS.

4616087, Oct 7, 1986

May 21, 1982

6/380642

Steven G. Wood - Orem UT

The Dow Chemical Company - Midland MI

C07D21172, C07D21184

546294

A process for preparing substituted-pyridines having a sulfonyl type substituted at the 3 or 5 position of the pyridine ring and a phenoxy type substituent at the 2 position is described.

5316768, May 31, 1994

Sep 11, 1992

7/943748

Bronwyn G. Hughes - Orem UT
Steven G. Wood - Orem UT

Murdock International Corporation - Springville UT

A61K 3578

424433

The present invention is directed to the use of antiviral compounds having the following generalized structure: ##STR1## wherein R is 2H or. dbd. O; R' is OH, H, or COOH (single substitution); and R" is OH, H, or alkyl; and pharmaceutically acceptable salts thereof as therapeutic substances having antiviral activity against human cytomegalovirus ("HCMV") and for treating diseases caused by HCMV. Dimeric forms of the forgoing antiviral compounds having antiviral activity against HCMV are also disclosed. Pharmaceutical compositions containing the disclosed antiviral compounds are disclosed for topical and systemic administration.

4371537, Feb 1, 1983

Aug 13, 1981

6/292467

Lowell D. Markley - Midland MI
Yulan C. Tong - Walnut Creek CA
Steven G. Wood - Orem UT

The Dow Chemical Company - Midland MI

A61K 3144, C07D21263

424263

Sulfur-substituted phenoxypyridines having antiviral activity are disclosed. Methods of using the sulfur-substituted phenoxypyridines to employ their antiviral activity are also disclosed as well as pharmaceutically-acceptable compositions thereof.