Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Todd M. Baughman"'
Autor:
Zhiping Xiong, Jeffrey J. Pouliot, Daniel J. Price, Andrew Maynard, Dulce Garrido, Andrew J. Peat, Katrina L. Creech, Todd M. Baughman, John W. Seal, Vincent W.-F. Tai, Luz Helena Kryn
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 24:2288-2294
Two novel series of spirocyclic piperidine analogs appended to a pyrazolo[1,5-a]pyridine core were designed, synthesized and evaluated for their anti-HCV activity. A series of piperidine ketals afforded dispiro 6p which showed excellent in vitro anti
Autor:
Emile J. Velthuisen, Todd M. Baughman, Brian A. Johns, David P. Temelkoff, Jason G. Weatherhead
Publikováno v:
European Journal of Medicinal Chemistry. 63:202-212
Several highly deuterated analogs of the HIV-1 protease inhibitor brecanavir have been prepared to study the effect of deuterium upon metabolic stability. The sites for deuterium incorporation were initially chosen to maximize the potential for a kin
Publikováno v:
Rapid Communications in Mass Spectrometry. 23:2146-2150
Propranolol is a widely used quality control and validation compound for liver microsome and hepatocyte metabolism studies. A multitude of literature reports describing the identification of propranolol metabolites exists today. However, no literatur
Autor:
Robert J. Barnaby, Cosette J. Serabjit-Singh, Luigina Bertolotti, Joseph W. Polli, Todd M. Baughman, Joan E. Humphreys, Angela L. Mote, Giovanni Vitulli, Kevin D. Read, Lindsey O. Webster, Kelly H. Jordan
Publikováno v:
Drug Metabolism and Disposition. 32:722-726
This article is available online at http://dmd.aspetjournals.org ABSTRACT: GV196771 (E-4,6-dichloro-3-(2-oxo-1-phenyl-pyrrolidin-3-glyden- emethyl)-1H-indole-2 carboxylic acid) is a potent antagonist of the modulatory glycine site of the N-methyl-D-a
Autor:
Jo A. Salisbury, Joan E. Humphreys, Cosette J. Serabjit-Singh, Todd M. Baughman, Timothy K. Tippin, Kelly H. Jordan, Joseph W. Polli, Angela L. Mote
Publikováno v:
Journal of Pharmaceutical Sciences. 92:2082-2089
Recent in vitro studies have suggested that P-glycoprotein (Pgp) and passive membrane permeability may influence the brain concentrations of non-sedating (second-generation) antihistamines. The purpose of this study was to determine the importance of
Publikováno v:
Rapid communications in mass spectrometry : RCM. 23(14)
Propranolol is a widely used quality control and validation compound for liver microsome and hepatocyte metabolism studies. A multitude of literature reports describing the identification of propranolol metabolites exists today. However, no literatur
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 852(1-2)
A hydrophilic interaction chromatography (HILIC)/mass spectrometric assay was developed for the determination of zanamivir, a neuraminidase inhibitor used to treat influenza, in rat and monkey plasma. An organic solvent with hydrophilic properties, m
Autor:
L. O. Tyler, Z. Zhao, M. Wells-Knecht, R. A. Graham, I. S. Silver, Todd M. Baughman, K. Wells-Knecht
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 33(6)
Pioglitazone is in the class of compounds known as the thiazolidinediones and is used to treat type 2 diabetes mellitus. The first in its class compound, troglitazone, was withdrawn from the U.S. market in 2000 due to a high incidence of hepatotoxici
Autor:
William F. Elmquist, Jin Cao, William J. Ehlhardt, Bryan H. Norman, Anne H. Dantzig, Michael Gregory Bell, Chuan Shih, James J. Starling, Joseph Michael Gruber, Todd M. Baughman, Mark A. Winter, Kevin L. Law, Julian Stanley Kroin, Robert L. Shepard
Publikováno v:
Advances in enzyme regulation. 37
The above data indicate that LY335979 displays the following characteristics of an 'ideal modulator' of Pgp-mediated multidrug resistance: high affinity binding to Pgp, high potency for in vitro reversal of drug resistance, high therapeutic index (ac
Publikováno v:
Chemosphere. 31(2)
The urinary metabolites of n-nonane in male Fischer 344 rats, after administering the hydrocarbon by gavage, included gamma-valerolactone, delta-hexanolactone, 2,5-hexanedione, delta-heptanolactone, 1-heptanol, 2-nonanol, 3-nonanol, 4-nonanol, 4-nona