Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Ernest S. Paight"'
Autor:
Marlys Hammond, David A. Griffith, Philip A. Carpino, Steven R. Schneider, Robert L. Dow, Paul DaSilva-Jardine, John R. Hadcock, Philip A. Iredale, Dennis O. Scott, Ernest S. Paight
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:5351-5354
A new series of CB(1) receptor antagonists incorporating an imidazole-based isosteric replacement for the hydrazide moiety of rimonabant (SR141716) is disclosed. Members of this imidazole series possess potent/selective binding to the rCB(1) receptor
Autor:
Robert L. Dow, Paul DaSilva-Jardine, Ernest S. Paight, Philip A. Carpino, David A. Griffith, John R. Hadcock, Philip A. Iredale, Dennis O. Scott, Rebecca E. O’Connor, Chudy I. Nduaka, Shawn C Black, Steven R. Schneider
Publikováno v:
Journal of Medicinal Chemistry. 52:2652-2655
We report the design, synthesis, and structure-activity relationships of novel bicyclic lactam-based cannabinoid type 1 (CB(1)) receptor antagonists. Members of these series are potent, selective antagonists in in vitro/in vivo efficacy models of CB(
Autor:
Steven W. Muchmore, Elizabeth A. Kowaluk, Kennan C. Marsh, Steve McGaraughty, Haixia Yu, Arthur Gomtsyan, Andrew O. Stewart, Shripad S. Bhagwat, Michael F. Jarvis, Karen M. Alexander, Kathy L. Kohlhaas, Clarissa L. Jakob, Chih-Hung Lee, Robin R. Frey, Mark A. Matulenko, Ernest S. Paight, Joseph P. Mikusa, Meiqun Jiang, Stanley Didomenico
Publikováno v:
Bioorganic & Medicinal Chemistry. 15:1586-1605
A series of non-nucleoside adenosine kinase (AK) inhibitors is reported. These inhibitors originated from the modification of 5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-ylamine (ABT-702). The identification of a linker
Autor:
Paul DaSilva-Jardine, Josephine Spitzer, Michele H. Rosner, Samuel P. Simons, Diane M. Hargrove, Boris A. Chrunyk, Richard F. Hank, Phoebe Chiang, Ernest S. Paight, Swick Andrew Gordon, Robert L. Dow, Peter Cornelius, Gayle K. Schulte, Tate Bonnie Frances, Steven R. Schneider, Terrell A. Patterson, William P. Newsome, Jayvardhan Pandit, Mark Ammirati, Eunsun Lee, Dennis E. Danley, Peter K. LeMotte
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:379-382
In this communication, we wish to describe the discovery of a novel series of 6-azauracil-based thyromimetics that possess up to 100-fold selectivities for binding and functional activation of the beta(1)-isoform of the thyroid receptor family. Struc
Publikováno v:
Polyhedron. 16:3505-3510
The synthesis and characterisation of some anionic Ni, Pd and Pt complexes of the ligand, Na2C3S5, (C3S52− = 1,3-dithiole-2-thione-4,5-dimercapto = dmit) are reported. The complexes were isolated as PPN+ [PPN+ = bis(triphenylphosphine)iminium] salt
Publikováno v:
Journal of Organometallic Chemistry. 466:283-289
Trimethylplatinum(IV) iodide reacts with ditellurides, R 2 Te 2 , to give bimetallic complexes of the type [(PtIMe 3 ) 2 (Te 2 R 2 )] (R = Me, p -MeOC 6 H 4 , p -EtOC 6 H 4 ). Ditelluroethers, RTeCH 2 TeR, react with trimethylplatinum(IV) iodide to g
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :3341-3347
Reaction of the dimercapto disodium salt 2 with 1,4-dibromobutane, dibromo-o-xylene, 1,8-bis(bromomethyl) naphthalene and 1,2,4,5-tetrakis(bromomethyl)benzene gave the thiones 3, 5, 8 and 11 respectively. The thiones 5 and 8 were oxidised to give the
Autor:
J. P. Jasinski, Ernest S. Paight
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:531-533
The coumarin and benzothiazolyl ring systems in the title compound, C 20 H 18 N 2 O 2 S, are planar. The pyrone ring in the coumarin moiety is bent slightly (2.30 o ) compared to the thiazolyl ring in the benzothiazolyl moiety. The crystal structure
Autor:
J. P. Jasinski, Ernest S. Paight
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 50:1928-1930
This molecule represents a new polymorph of the title laser-dye aminocoumarin compound, C 12 H 10 F 3 NO 2 . Torsion angles in the trifluoro moiety and intermolecular packing effects indicate significant structural differences when compared to its po
Publikováno v:
The Journal of Organic Chemistry. 56:710-712