Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Catherine A. Dyke"'
Publikováno v:
Journal of Chromatography A. 523:300-304
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f281a2e04468f6e618637c6b679bf657
https://doi.org/10.1016/0021-9673(90)85033-r
https://doi.org/10.1016/0021-9673(90)85033-r
Autor:
Patrick Camilleri, Catherine A. Dyke
Publikováno v:
Journal of Chromatography A. 518:277-281
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::360e75d05bca3c7287dd64a5467c1828
https://doi.org/10.1016/s0021-9673(01)93189-9
https://doi.org/10.1016/s0021-9673(01)93189-9
Autor:
Patrick Camilleri, Christopher J. Thorpe, David G. Reid, Catherine A. Dyke, Simon P. Robinson, Lesley K. MacLachlan
Publikováno v:
Chirality. 2:229-232
1H nuclear magnetic resonance at 360 MHz shows that SK&F 96365 (1-(beta-[3-(p-methoxyphenyl)-propyloxy]-p-methoxyphenethyl)-1H- imidazole hydrochloride), an antagonist of mammalian receptor-operated calcium channels, interacts with the calcium-bindin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0654205c248b664a0a6fa632b8905c1
https://doi.org/10.1002/chir.530020407
https://doi.org/10.1002/chir.530020407
Publikováno v:
Journal of Chromatography A. 498:414-416
In this Note we describe an analytical method that is suitable to differentiate between the optical isomers of fenoldopam. This method was also used to resolve the optical isomers, where the three hydroxy groups in fenoldopam have been replaced by me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::538a8554004ffbee17d55579f8a627bf
https://doi.org/10.1016/s0021-9673(01)84271-0
https://doi.org/10.1016/s0021-9673(01)84271-0
Autor:
Robert John Ife, Catherine A. Dyke, Eugene Meenan, David J. Keeling, Anthony H. Underwood, Colin J. Theobald, Carolyn A. Price, Michael E. Parsons, Malcolm L. Meeson
Publikováno v:
Journal of Medicinal Chemistry. 32:1970-1977
The benzimidazole sulfoxide class of antisecretory H+/K+-ATPase inhibitors need to possess high stability under neutral physiological conditions yet rearrange rapidly at low pH to the active sulfenamide 2. Since the initial reaction involves internal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9575bd815ecd39e34bd813afcef7ec7
https://doi.org/10.1021/jm00128a046
https://doi.org/10.1021/jm00128a046