R D Dyer - JoVE Visualize

Showing results (21-30 of 28) with videos related to

Pageof 3

Sort By:

You have reached the last page of results.This site can display upto 28 results.

Journal of Medicinal Chemistry|January 21, 1994

Synthesis and biological evaluation of 5-[[3,5-bis(1,1-dimethylethyl)- 4-hydroxyphenyl]methylene]oxazoles, -thiazoles, and -imidazoles: novel dual 5-lipoxygenase and cyclooxygenase inhibitors with antiinflammatory activityP C Unangst, D T Connor, W A Cetenko, et al.

Journal of Medicinal Chemistry|June 25, 1993

1,3,4-Oxadiazole, 1,3,4-thiadiazole, and 1,2,4-triazole analogs of the fenamates: in vitro inhibition of cyclooxygenase and 5-lipoxygenase activitiesD H Boschelli, D T Connor, D A Bornemeier, et al.

Journal of Medicinal Chemistry|January 29, 2000

Structure-activity relationships and pharmacokinetic analysis for a series of potent, systemically available biphenylsulfonamide matrix metalloproteinase inhibitorsP M O'Brien, D F Ortwine, A G Pavlovsky, et al.

Journal of Medicinal Chemistry|October 1, 1988

Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesisJ B Summers, B P Gunn, J G Martin, et al.

Bioorganic & Medicinal Chemistry|April 1, 1995

Hydroxylamine analogs of 2,6-di-t-butylphenols: dual inhibitors of cyclooxygenase and 5-lipoxygenase or selective 5-lipoxygenase inhibitorsJ B Kramer, T Capiris, J C Sircar, et al.

Prostaglandins|January 1, 1994

The pharmacologic effects of 5-[3,5-bis(1,1-dimethylethyl)-4- hydroxyphenyl]-1,3,4-thiadiazole-2(3H)-thione, choline salt (CI-986), a novel inhibitor of arachidonic acid metabolism in models of inflammation, analgesia and gastric irritationD J Schrier, V M Baragi, D T Connor, et al.

Journal of Medicinal Chemistry|April 10, 1999

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone seriesY Song, D T Connor, R Doubleday, et al.

Journal of Medicinal Chemistry|April 10, 1999

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1,3,4- and 1,2,4-thiadiazole seriesY Song, D T Connor, A D Sercel, et al.

Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 28 results.

Journal of Medicinal Chemistry|January 21, 1994

Synthesis and biological evaluation of 5-[[3,5-bis(1,1-dimethylethyl)- 4-hydroxyphenyl]methylene]oxazoles, -thiazoles, and -imidazoles: novel dual 5-lipoxygenase and cyclooxygenase inhibitors with antiinflammatory activityP C Unangst, D T Connor, W A Cetenko, et al.

Journal of Medicinal Chemistry|June 25, 1993

1,3,4-Oxadiazole, 1,3,4-thiadiazole, and 1,2,4-triazole analogs of the fenamates: in vitro inhibition of cyclooxygenase and 5-lipoxygenase activitiesD H Boschelli, D T Connor, D A Bornemeier, et al.

Journal of Medicinal Chemistry|January 29, 2000

Structure-activity relationships and pharmacokinetic analysis for a series of potent, systemically available biphenylsulfonamide matrix metalloproteinase inhibitorsP M O'Brien, D F Ortwine, A G Pavlovsky, et al.

Journal of Medicinal Chemistry|October 1, 1988

Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesisJ B Summers, B P Gunn, J G Martin, et al.

Bioorganic & Medicinal Chemistry|April 1, 1995

Hydroxylamine analogs of 2,6-di-t-butylphenols: dual inhibitors of cyclooxygenase and 5-lipoxygenase or selective 5-lipoxygenase inhibitorsJ B Kramer, T Capiris, J C Sircar, et al.

Prostaglandins|January 1, 1994

The pharmacologic effects of 5-[3,5-bis(1,1-dimethylethyl)-4- hydroxyphenyl]-1,3,4-thiadiazole-2(3H)-thione, choline salt (CI-986), a novel inhibitor of arachidonic acid metabolism in models of inflammation, analgesia and gastric irritationD J Schrier, V M Baragi, D T Connor, et al.

Journal of Medicinal Chemistry|April 10, 1999

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone seriesY Song, D T Connor, R Doubleday, et al.

Journal of Medicinal Chemistry|April 10, 1999

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1,3,4- and 1,2,4-thiadiazole seriesY Song, D T Connor, A D Sercel, et al.

Pageof 3