Zobrazeno 1 - 10
of 28
pro vyhledávání: '"J. E. Bakke"'
Publikováno v:
Xenobiotica. 22:325-334
1. Pentachlorophenyl methyl sulphoxide and pentachlorophenyl methyl sulphone were found to be substrates for microsomal and cytosolic glutathione-S-transferase of rabbit, monkey, chicken and human liver, covalently immobilized on beaded sepharose. 2.
Autor:
J. E. Bakke
Publikováno v:
Drug Metabolism Reviews. 22:637-647
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 30(12)
1. Radioactivity from oral doses of N-isopropyl[1-14C]acetanilide was excreted in urine (53.5%), faeces (8.1%) and expired air (17.0%) of rat. 2. Enterohepatic circulation occurred during formation of approximately 34% of the metabolites. N-isopropyl
Publikováno v:
Circulation. 94
Cardiac transplantation is an increasingly important treatment for patients with end-stage heart failure. Rejection is one of the major limitations, and currently, serial endomyocardial biopsies are required to diagnose rejection. In the year after t
Publikováno v:
ACS Symposium Series ISBN: 9780841227385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::924011ea6909783c3d9ce31e06f17fbb
https://doi.org/10.1021/bk-1992-0542.ch011
https://doi.org/10.1021/bk-1992-0542.ch011
Metabolism of the glutathione conjugate of propachlor by in situ perfused kidneys and livers of rats
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 20(4)
1. [1-14C]Propachlor-GSH was perfused at 0.34, 3.4 and 34 mumol/h through the portal vein or the right renal artery of anaesthetized rats with biliary and ureteral cannulas. Urine was the predominant route for elimination of the 14C regardless of the
Autor:
J. E. Bakke
Publikováno v:
Biological Mass Spectrometry. 19:635-635
Autor:
K. E. Norin, J. E. Bakke, Joseph Rafter, Jan-Åke Gustafsson, Gerald L. Larsen, Bertil Gustafsson
Publikováno v:
Xenobiotica. 13:171-178
Conventional rats metabolize 2-chloro-N-isopropylacetanilide (propachlor) mainly to various 2-methylsulphonylacetanilides and to residues in the faeces that are unextractable. Mercapturic acid pathway (MAP) metabolites of propachlor are the source of
Autor:
C. E. Price, J. E. Bakke
Publikováno v:
Journal of Environmental Science and Health, Part B. 14:279-290
Rats excreted the 14C from a single oral dose of N‐isopropyl‐N‐[14C]phenyloxamic acid [I, a soil metabolite from 2‐chloro‐N‐isopropylacetanilide (propachlor)] in approximately equal quantities in the urine (49.2%) and feces (48.2%). A mil
Autor:
J. E. Bakke, C. E. Price
Publikováno v:
Journal of Environmental Science and Health, Part B. 11:9-22
Sheep and rats metabolized single oral doses of O-O-dimethyl-O-(3,5,6-trichloro-2-pyridyl) phosphorothioate (I) to three major metabolites that were excreted in the urine (approximately 70% of the 14C). These were the glucuronide of 3,5,6-trichloro-2