Zobrazeno 1 - 10
of 24
pro vyhledávání: '"K. Gerding"'
Autor:
M. Sausen, J. Hernandez, L. Keefer, S. Angiouli, F. Cavallo, J. Simmons, K. Gerding, Siân Jones, James R. White
Publikováno v:
Journal of Thoracic Oncology. 13:S985-S986
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22e9cfc5c0abe98dcab5c6b388268230
https://doi.org/10.1016/j.jtho.2018.08.1866
https://doi.org/10.1016/j.jtho.2018.08.1866
Background: Exacerbations represent a major source of morbidity and mortality in asthma and are a prominent feature of poorly controlled, difficult-to-treat disease. Objective: The goal of our study was to provide a detailed characterization of the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::5c9045af70633e63c55d6459b347f030
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3001909
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3001909
Publikováno v:
Packaging Technology and Science, 3, 9, 153-165
Packaging foodstuffs is a dynamic process which continually has to respond to the changes in supply and demand which are the result of adaptations to the varying demands of the consumer, changes in retail practices, technological innovations, new mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90734c0eaa4d0a8b0f07817d7ceda605
https://doi.org/10.1002/pts.2770090305
https://doi.org/10.1002/pts.2770090305
Publikováno v:
Journal of Chromatography A. 625:223-230
Tetracyclic eudistomins, a class of compounds with potent antiviral and antitumour activity, contain two asymmetric centres, resulting into two (d,l) pairs called “cis” and “trans”. The cis-enatiomers can be separated on the chiral stationary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21dcb66094f2b30e56302451304ebf41
https://doi.org/10.1016/0021-9673(92)85206-9
https://doi.org/10.1016/0021-9673(92)85206-9
Publikováno v:
Xenobiotica. 20:515-524
1. The disposition and metabolic profiling of 2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin(I), a dopamine agonist, were studied in anaesthetized rats after i.v. administration and in non-anaesthetized rats after i.v. and oral dosing. No major
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73a98539c373d81db9a401e10796c53a
https://doi.org/10.3109/00498259009046866
https://doi.org/10.3109/00498259009046866
Publikováno v:
Electrophoresis. 25(16)
A capillary electrophoresis method for the enantiomeric purity determination of SLV307, a basic potential antipsychotic compound, has been developed and validated. It is shown that the presence of the eutomer in the sample solution may have a signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb5691cd8431d326c9fd8f7cf639e8f
https://pubmed.ncbi.nlm.nih.gov/15352019
https://pubmed.ncbi.nlm.nih.gov/15352019
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 19(1)
Glucuronidation is known to be a major metabolic pathway for labetalol. As the drug contains a phenolic and an alcoholic hydroxy group, in principle two regio isomeric glucuronides can be formed. By incubating the substrate labetalol with bovine live
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ce8a72203c4c83e207d875696230e4b
https://pubmed.ncbi.nlm.nih.gov/1673399
https://pubmed.ncbi.nlm.nih.gov/1673399
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 18(6)
The metabolism of 2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin (N-0437) was investigated in conscious monkeys after subsequent i.v., oral, and ocular administration. The administration of the drug caused some physiological effects, such as br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26d752a8353a1bb7b6d555d2bf801d61
https://pubmed.ncbi.nlm.nih.gov/1981538
https://pubmed.ncbi.nlm.nih.gov/1981538
Publikováno v:
Experimental eye research, 51(1), 11-14. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD
The ocular and systemic disposition of the new dopamine agonist 2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin (N-0437) was investigated in conscious monkeys after ocular administration of 0.56 mg N-0437. HCl (corresponding to 0.50 mg free base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd26663ddce6f1ee94c642972b09d87
https://pubmed.ncbi.nlm.nih.gov/1973654
https://pubmed.ncbi.nlm.nih.gov/1973654
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 20(5)
1. The in vivo metabolic pathways of 2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin (I) in rats have been established, using in vitro metabolism as a complementary technique. 2. All identified metabolites were conjugates. Glucuronidation at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2301aa339ed352f09055670464151ea
https://pubmed.ncbi.nlm.nih.gov/1971984
https://pubmed.ncbi.nlm.nih.gov/1971984