Zobrazeno 1 - 7
of 7
pro vyhledávání: '"James M. Grace"'
Autor:
James M. Grace, Thomas G. Brewer, Alan L. Mitchell, Kathleen U. Leo, Jim O. Peggins, Tony Aguilar, Qigui Li
Publikováno v:
Pharmacology. 54:276-284
Arteether (AE) is primarily deethylated to dihydroqinghaosu (DQHS) in rats and humans. Conversion of AE to DQHS was impaired in microsomes from rats infected with Plasmodium berghei. The Km for AE was 175.1 +/- 49.1 and 124.4 +/- 115.1 mumol/l, and V
Publikováno v:
Pharmaceutical Research. 14:1449-1454
Purpose. To study the reaction of artelinic acid with chemical model systems of cytochrome P-450 as a means of obtaining authentic samples of the putative metabolites necessary for identification of the mammalian metabolites of artelinic acid.
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1643-1648
Amonafide (4-aminobenzoisoqinolinedione) and its structural analog, mitonafide 1 , have been shown to stabilize topoisomerase II cleavable complexes. The position of the nitro group and structural modifications of the side chain influence the interac
Publikováno v:
Chemical Research in Toxicology. 7:286-290
Debrisoquine 4-hydroxylase is a unique cytochrome P450 that effects oxidation of protonated substrates at sites distal from the basic nitrogen. A basic tenet of the several models that have been proposed for the active site of P450 2D6 is that oxidat
Autor:
Steven L. Andersen, Jonathan L. Vennerstrom, Joanna K. Hu, James M. Grace, Arba L. Ager, Varima Wongpanich, David L. Wesche, Cindy K. Angerhofer
Publikováno v:
The American journal of tropical medicine and hygiene. 62(5)
The antimalarial peroxide, dispiro-1,2,4,5-tetraoxane WR 148999, was synergistic with chloroquine, quinine, mefloquine, and artemisinin against both D6 and W2 clones of Plasmodium falciparum. In consideration of the contrasting antagonism between art
Publikováno v:
Clinical pharmacokinetics. 39(4)
Various compounds of the artemisinin family are currently used for the treatment of patients with malaria worldwide. They are characterised by a short half-life and feature the most rapidly acting antimalarial drugs to date. They are increasingly bei
Publikováno v:
Free radical research. 25(1)
Products of the reaction of 4-hydroxy-2-nonenal (4HNE) with native and heat-denatured Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase (G6PDH) were analyzed to determine the structure and position of the protein modifications. Matrix assis