Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jeffery J Prusakiewicz"'
Autor:
Terry P. Lybrand, Jeffery J. Prusakiewicz, Christopher W. Moth, Anna L. Blobaum, Dapo Akingbade, Shu Xu, Carol A. Rouzer, Aaron T. Jacobs, Kebreab Ghebreselasie, Lawrence J. Marnett, Mary E. Konkle
Publikováno v:
Biochemistry
The cyclooxygenase enzymes (COX-1 and COX-2) are the therapeutic targets of nonsteroidal anti-inflammatory drugs (NSAIDs). Neutralization of the carboxylic acid moiety of the NSAID indomethacin to an ester or amide functionality confers COX-2 selecti
Autor:
Hassan Rashidzadeh, Anneli Savinainen, Justine Oswald, Elizabeth Spencer, Marita Larsson Cohen, Zhen Lou, Jeffery J Prusakiewicz, Serene Josiah
Publikováno v:
Experimental Eye Research. 189:107836
TAK-639 is a topical, 9–amino acid, synthetic, C-type natriuretic peptide analog in development for the treatment of primary open-angle glaucoma and ocular hypertension. This study investigated the impact of TAK-639 on intraocular pressure (IOP), t
Autor:
Justyna Korczynska, Lemy Tsikna, Zoe Hughes-Thomas, Richard Haworth, Christopher J. Roberts, John Warrack, Steven D. Sorden, Irene Papanicolaou, Rodd Polsky, Eric Dobrzynski, Edit Kurali, Timothy Streit, Thomas Wilde, Jeffery J Prusakiewicz, Brian J Christian, Peter C. Adamson, T Michael Nork, Ian Richard Catchpole, Craig Struble, Caroline Sychterz, James Walford, Chi-Man Tang, Daniel Gibson, Ruud Verrijk, Paul E. Miller, Fiona Cook, Jos Smal
Publikováno v:
Journal of controlled release : official journal of the Controlled Release Society
A potent anti-vascular endothelial growth factor (VEGF) biologic and a compatible delivery system were co-evaluated for protection against wet age-related macular degeneration (AMD) over a 6month period following a single intravitreal (IVT) injection
Autor:
Elizabeth Groeber, Joe Palandra, Lori Christine, Jeffery J. Prusakiewicz, Ann D. Wrightstone, Udeni Yapa, Arthur J. Wittwer
Publikováno v:
Analytical Biochemistry. 421:556-565
Fatty acid amide hydrolase (FAAH) is one of the main enzymes responsible for the degradation of the endocannabinoid anandamide (N-arachidonoylethanolamine, AEA). FAAH inhibitors may be useful in treating many disorders involving inflammation and pain
Autor:
Jeffery J. Prusakiewicz, Gwendolyn D. Fate, Richard Voorman, Chrisita Ackermann, Faith M. Williams, Christopher Jewell, N. Ann Payne
Publikováno v:
Toxicology and Applied Pharmacology. 225:221-228
Parabens are esters of 4-hydroxybenzoic acid and used as anti-microbial agents in a wide variety of toiletries, cosmetics and pharmaceuticals. It is of interest to understand the dermal absorption and hydrolysis of parabens, and to evaluate their dis
Autor:
Christopher Jewell, Jeffery J. Prusakiewicz, N. Ann Payne, Gwendolyn D. Fate, Chrisita Ackermann, Faith M. Williams
Publikováno v:
Toxicology Letters. 173:118-123
Skin esterases serve an important pharmacological function as they can be utilised for activation of topically applied ester prodrugs. Understanding the nature of these enzymes, with respect to their role and local activity, is essential to defining
Autor:
Ahmad H. Al-Mestarihi, Melissa V. Turman, Vincenzo Di Marzo, Andrew Vila, Jeffery J. Prusakiewicz, Heather L. Ball, Lawrence J. Marnett
Publikováno v:
Archives of Biochemistry and Biophysics. 464:260-268
The lipoamino acids and endovanilloids have multiple roles in nociception, pain, and inflammation, yet their biological reactivity has not been fully characterized. Cyclooxygenases (COXs) and lipoxygenases (LOs) oxygenate polyunsaturated fatty acids
Autor:
Jeffery J. Prusakiewicz, Heather M. Harville, Yanhua Zhang, Richard Voorman, Chrisita Ackermann
Publikováno v:
Toxicology. 232:248-256
Parabens ( p -hydroxybenzoate esters) are a group of widely used preservatives in topically applied cosmetic and pharmaceutical products. Parabens display weak associations with the estrogen receptors in vitro or in cell based models, but do exhibit
Publikováno v:
Current Pharmaceutical Design. 10:659-667
The last decade has witnessed a rapid expansion in our understanding of the mammalian endogenous cannabinoid system. In just a few short years since the discovery of endogenous lipids that serve as cannabinoids in vivo, these molecules have been show
Autor:
Kevin R. Kozak, Lawrence J. Marnett, Scott W. Rowlinson, Jeffery J. Prusakiewicz, Daniel R. Prudhomme
Publikováno v:
Biochemistry. 42:9041-9049
The endocannabinoid arachidonylethanolamide (AEA, anandamide) is an endogenous ligand for the cannabinoid receptors and has been shown to be oxygenated by cyclooxygenase-2 (COX-2). We examined the structural requirements for COX-mediated, AEA oxygena