Zobrazeno 1 - 10
of 14
pro vyhledávání: '"William B. Mahony"'
Publikováno v:
Biochemical Pharmacology. 46:725-729
The mechanism of membrane permeation of several 2′,3′-dideoxynucleosides was investigated at 37° with human erythrocytes using an “inhibitor-stop” assay. Transport (per 5 μL cells) via the nucleoside and nucleobase carriers was assessed by
Publikováno v:
Biochemical Pharmacology. 42:147-152
The mechanism of transport of desciclovir (DCV)--a structural analogue and prodrug of acyclovir (ACV) which provides an improved oral bioavailability of ACV--was investigated in human erythrocytes with a "papaverine-stop" assay. DCV influx was noncon
Publikováno v:
Biochemical Pharmacology. 41:263-271
The membrane permeation of ganciclovir (DHPG)--a structural analogue of acyclovir (ACV) with activity against cytomegalovirus--was investigated in human erythrocytes at 37 degrees with an "inhibitor-stop" assay. DHPG influx was nonconcentrative, occu
Publikováno v:
Biochemical pharmacology. 68(9)
Abacavir, (-)-(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol, is a novel purine carbocyclic nucleoside analogue that has been approved by the FDA for the treatment of HIV (as Ziagen trade mark [abacavir sulfate]). Ch
Autor:
Geoffrey J. Yuen, Nancy F. Thompson, H. Wayne Hutman, Yu Lou, Thurman Allsup, Victoria R. Otto, William B. Mahony
Publikováno v:
Journal of clinical pharmacology. 41(3)
A single-center, open-label, three-way crossover study was conducted in 24 healthy subjects to assess (1) the bioequivalence of a combined abacavir 300 mg/lamivudine 150 mg/zidovudine 300 mg (A/L/Z) combination tablet relative to the separate brand-n
Publikováno v:
Biochemical pharmacology. 46(3)
The transport of 5-fluorouracil (5-FU) and uracil into human erythrocytes has been investigated under initial velocity conditions with an "inhibitor-stop" assay using a cold papaverine solution to terminate influx. At 37 degrees and pH 7.3, 5-FU infl
Publikováno v:
Journal of Biological Chemistry. 262:5748-5754
The demonstrated in vitro and in vivo activity of 3′-azido-3′-deoxythymidine (N3dThd) against the infectivity and the cytopathic effect of human immunodeficiency virus has prompted an investigation of the mechanism by which this nucleoside analog
Publikováno v:
Journal of Biological Chemistry. 263:9276-9284
A novel "inhibitor-stop" method for the determination of initial rates of purine nucleobase transport in human erythrocytes has been developed, based on the addition of seven assay volumes of cold 19 mM papaverine to terminate influx. In view of our
Autor:
Thomas P. Zimmerman, William B. Mahony
Publikováno v:
Analytical Biochemistry. 154:235-243
5-[125I]Iodo-2'-deoxyuridine (IdUrd) has been shown to serve as a permeant for the nucleoside transport system of human erythrocytes and to be matabolically inert in these cells. Linear initial velocities were obtained at 20 degrees C for 125IdUrd tr
Publikováno v:
Journal of Biological Chemistry. 263:9285-9291
The mechanism of transport of the antiviral agent acyclovir (ACV) into human erythrocytes has been investigated. Initial velocities of ACV influx were determined with an "inhibitor-stop" assay that used papaverine to inhibit ACV influx rapidly and co