Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Dominick DelGrande"'
Autor:
Paivi Jaana Kukkola, Suraj S. Shetty, Natalie A. Bilci, Paula Savage, Theodore Ikler, Arco Y. Jeng, Dominick DelGrande
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:1737-1740
1,3-Disubstituted isoindolines have been discovered as a new class of potent functional ET A selective receptor antagonists through pharmacophore analysis of existing nonpeptide endothelin antagonists. The structure–activity relationships for both
Autor:
Gary M. Coppola, Xilin Liu, Robert C. Anderson, Douglas C. Knorr, William S. Fillers, James L. Stanton, Jiaping Gao, Tomaselli Hc, Christine C. Vinluan, Thomas Daniel Aicher, Carol J. Dragland, Suraj S. Shetty, Wieslawa Maniara, A. Islam, Emma L. Kaplan, William R. Mann, Leonard J. Brand, Donald Mark Sperbeck, R. E. Walter, Dominick DelGrande, R. J. Lozito
Publikováno v:
Journal of Medicinal Chemistry. 43:236-249
N‘-Methyl-N-(4-tert-butyl-1,2,5,6-tetrahydropyridine)thiourea, SDZ048-619 (1), is a modest inhibitor (IC50 = 180 μM) of pyruvate dehydrogenase kinase (PDHK). In an optimization of the N-methylcarbothioamide moiety of 1, it was discovered that amid
Autor:
Emma L. Kaplan, Gary M. Coppola, Xilin Liu, Gregory Raymond Bebernitz, Donald Mark Sperbeck, Dominick DelGrande, Wieslawa Maniara, Leonard J. Brand, Suraj S. Shetty, Thomas Daniel Aicher, Robert C. Anderson, Charles F. Jewell, R. J. Lozito, Douglas C. Knorr, A. Islam, Chen Liu, Christine C. Vinluan, Jianping Gao, Robert J. Strohschein, William R. Mann, Carol J. Dragland, R. E. Walter
Publikováno v:
Journal of Medicinal Chemistry. 42:2741-2746
Publikováno v:
Biochemical and Biophysical Research Communications. 191:459-464
IRL 1620 (Suc-[Glu9,Ala11,15]-ET-1 (8-21)) (0.1 nM - 1 microM), a novel ETB-selective endothelin (ET) agonist, produced endothelium-dependent relaxations in precontracted rabbit mesenteric artery (2 nM, EC50) and endothelium-independent contractions
Autor:
Arco Y. Jeng, Dominick DelGrande, Natalie A. Bilci, Paula Savage, Paivi Jaana Kukkola, Suraj S. Shetty, Theodore Ikler
Publikováno v:
ChemInform. 32
1,3-Disubstituted isoindolines have been discovered as a new class of potent functional ET A selective receptor antagonists through pharmacophore analysis of existing nonpeptide endothelin antagonists. The structure–activity relationships for both
Autor:
Wei H. Wang, Christine C. Vinluan, Robert J. Strohschein, Xilin Liu, Emma L. Kaplan, Dominick DelGrande, Gregory Raymond Bebernitz, Douglas C. Knorr, Jennifer Tan, Jiaping Gao, Suraj S. Shetty, James L. Stanton, Charles Liu, Thomas Daniel Aicher, Carol J. Dragland, William R. Mann, Leonard J. Brand, Robert J. Lozito, Wieslawa Maniara, Amin Islam
Publikováno v:
Journal of medicinal chemistry. 43(11)
The optimization of a series of anilide derivatives of (R)-3,3, 3-trifluoro-2-hydroxy-2-methylpropionic acid as inhibitors of pyruvate dehydrogenase kinase (PDHK) is described that started from N-phenyl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide 1
Autor:
Shiling Hu, Joseph L. Balwierczak, Dominick DelGrande, Helen S. Kim, Christine M. Krulan, George B. Weiss
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 352(2)
The rank order of potency of a series of benzopyran and cyanoguanidine K+ channel openers (KCOs) for causing relaxation of the PGF2 alpha-precontracted porcine coronary artery was determined. Glyburide, an inhibitor of KATP channels, showed an appare
Publikováno v:
Journal of biochemistry. 112(1)
Endothelin-1 (ET-1) is a potent peptidic vasoconstrictor. This peptide has been shown to be cleared rapidly by the kidney. The purpose of the present study was to assess the involvement of renal proteolytic enzymes in the clearance/degradation of ET-
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