Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Graciela B Arhancet"'
Autor:
Scott A. Long, Zahra Shahrashoob, Guangzhe Yu, Brian P. Grady, Graciela B Arhancet, Jeffrey H. Harwell
Publikováno v:
Journal of Surfactants and Detergents. 22:95-102
Autor:
Scott A. Long, Jeffrey H. Harwell, Kyle A. Karinshak, Graciela B Arhancet, Guangzhe Yu, Brian P. Grady
Publikováno v:
Journal of Surfactants and Detergents. 20:503-519
Hydroxy-4-(methylthio)butanoic acid (HMTBA) is a commonly used animal feed additive available in large quantities. In this study, anionic surfactants were synthesized utilizing HMTBA as a starting material. Specifically, a straight- chain fatty acid
Autor:
Guangzhe Yu, Scott A. Long, Kyle A. Karinshak, Brian P. Grady, Jeff H. Harwell, Graciela B. Arhancet
Publikováno v:
Journal of Surfactants and Detergents. 18:895-903
Autor:
John Robert Springer, Gina M. Jerome, Hayes Michael J, Michael T. Baratta, Daniel P. Walker, Graciela B. Arhancet, Alexander F. Shaffer, Jaime L. Masferrer, Ben S. Zweifel, Steven E. Heasley, Darin E. Jones, William M. Moore, Jeffrey S. Carter, Yvette M. Fobian, Michael L. Vazquez, Sue Metz
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 23:1114-1119
Inhibition of mPGES-1, the terminal enzyme in the arachidonic acid/COX pathway to regulate the production of pro-inflammatory prostaglandin PGE2, is considered an attractive new therapeutic target for safe and effective anti-inflammatory drugs. The d
Autor:
Daniel P. Walker, Alexander F. Shaffer, William M. Moore, Michael T. Baratta, Sue Metz, Jeffrey A. Scholten, John Robert Springer, Jeffrey S. Carter, Hwang-Fun Lu, Steven E. Heasley, Yvette M. Fobian, Natasha M. Kablaoui, Francisco M. Franco, Li Xing, Shengtian Yang, Hanau Cathleen E, Michael L. Vazquez, Graciela B. Arhancet, Gina M. Jerome
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 23:1120-1126
Microsomal prostaglandin E(2) synthase-1 (mPGES-1) is a novel therapeutic target for the treatment of inflammation and pain. In the preceding letter, we detailed the discovery of clinical candidate PF-04693627, a potent mPGES-1 inhibitor possessing a
Autor:
Kaliappan Iyanar, Jessica D. Dietz, Graciela B. Arhancet, Horng-Chih Huang, Danny J. Garland, Marcia I. Heron, Silvia I. Pomposiello, Xiao Hu, Len F. Lee, Joe T. Collins, Scott S. Woodard, James Robert Blinn, Maria A. Payne, Brenda L. Case, Rhonda S. Woerndle
Publikováno v:
Journal of Medicinal Chemistry. 53:5970-5978
A new 1,4-dihydropyridine 5a, containing a cyano group at the C3 position, was recently reported to possess excellent mineralocorticoid receptor (MR) antagonist in vitro potency and no calcium channel-blocker (CCB) activity. In the present study, we
Autor:
Grace M. Wagner, Joe T. Collins, Scott S. Woodard, Randal E Numann, Kaliappan Iyanar, Graciela B. Arhancet, Danny J. Garland, James Robert Blinn, Jessica D. Dietz, Horng-Chih Huang, Xiao Hu
Publikováno v:
Journal of Medicinal Chemistry. 53:4300-4304
A number of known 1,4-dihydropyridine CCBs were identified as having comparable potency to the steroidal MR antagonist eplerenone. Chiral resolution of mebudipine revealed that MR and CCB activity reside in opposite enantiomers. Small molecule X-ray
Autor:
Charles W. Bolten, Patrick M. Blanner, William G. McDonald, Nicholas R. Staten, Richard A. Mazzarella, Graciela B. Arhancet, Martin F. Meier, David J. Weiss, Patrick M. Sullivan, Alexander E. Hromockyj, Rolf F. Kletzien, Jerry R. Colca
Publikováno v:
Gene Regulation and Systems Biology, Vol 1, Pp 73-82 (2007)
Gene Regulation and Systems Biology, Vol 1 (2007)
Gene Regulation and Systems Biology
Gene Regulation and Systems Biology, Vol 1 (2007)
Gene Regulation and Systems Biology
Insulin sensitizing thiazolidinediones (TZDs) are generally considered to work as agonists for the nuclear receptor peroxisome proliferative activated receptor-gamma (PPAR gamma). However, TZDs also have acute, non-genomic metabolic effects and it is
Autor:
Marvin J. Meyers, Paula M. Loria, Li She, Xiangyang Chen, David W. Piotrowski, Neil Raheja, Agustin Casimiro-Garcia, Kun Song, Catherine M. Ambler, Liuqing Wei, Graciela B. Arhancet, Derek Vrieze, Sandra M. Jennings, Carine M. Boustany-Kari, Catherine Angela Hulford, Rena Eudy, Cuiman Cai, Mary Ellen Banker, David Hepworth, Tereece Banks, Matthew F. Sammons, Donna N. Petersen
Publikováno v:
Journal of medicinal chemistry. 57(10)
A novel series of nonsteroidal mineralocorticoid receptor (MR) antagonists identified as part of our strategy to follow up on the clinical candidate PF-03882845 (2) is reported. Optimization departed from the previously described pyrazoline 3a and fo
Publikováno v:
The Journal of Organic Chemistry. 62:3537-3541
Alkoxyamine 3 undergoes thermolysis only on heating to over 150 °C, ΔH⧧ = 34.3 ± 1.6 kcal/mol and ΔS⧧ = 0.8 ± 3.7 eu. The initially formed nitroxyl (6) and α-phenethyl radicals (5) mainly disproportionate to styrene plus diethylhydroxylamin