Zobrazeno 1 - 10
of 184
pro vyhledávání: '"J. K. Stubbs"'
Autor:
Kenneth J. Blackburn, S F Campbell, Peter Edward Cross, Alan J. Higgins, Michael Gwilt, Donald G. Gardiner, Roger A. Burges, J K Stubbs
Publikováno v:
Journal of Cardiovascular Pharmacology. 9:110-119
Summary:Amlodipine was twice as potent as nifedipine at inhibiting Ca2 + -induced contractions in depolarised rat aorta (IC50 1.9 nM vs. 4.1 nM) but, unlike nifedipine, displayed a very slow onset of action. Contractions induced by depolarising steps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939d1ab483c14fd3a2a6fefc9f2b157d
https://doi.org/10.1097/00005344-198701000-00018
https://doi.org/10.1097/00005344-198701000-00018
Autor:
R. A. Burges, D. G. Gardiner, M. Gwilt, A. J. Higgins, K. J. Blackburn, S. F. Campbell, P. E. Cross, J. K. Stubbs
Publikováno v:
Journal Of Cardiovascular Pharmacology. 9:110-119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6efcdc08e41793d260300e623706bdd9
https://doi.org/10.1097/00005344-198709010-00018
https://doi.org/10.1097/00005344-198709010-00018
Autor:
John Edmund Arrowsmith, Campbell Simon F, J K Stubbs, Roger A. Burges, Donald G. Gardiner, Peter E. Cross, Kenneth J. Blackburn
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aa8201d79e44519bc4bdb6b02bb63a1
https://doi.org/10.1002/chin.198706180
https://doi.org/10.1002/chin.198706180
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::073dbc25fce7b4495a106400c35b5a2b
https://doi.org/10.1002/chin.197609246
https://doi.org/10.1002/chin.197609246
Autor:
J. K. Stubbs, R. M. Acheson
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1812c97d49c89111494f039a2a5a55a
https://doi.org/10.1002/chin.197003133
https://doi.org/10.1002/chin.197003133
Autor:
J. K. Stubbs, R. M. Acheson
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7270f1b5b2cc703e970dc219cd48db52
https://doi.org/10.1002/chin.197223281
https://doi.org/10.1002/chin.197223281
Autor:
R. M. Acheson, J. K. Stubbs
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a41bb86ecbd28d1bdee448df6a2b34ad
https://doi.org/10.1002/chin.197152329
https://doi.org/10.1002/chin.197152329
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:1440-1441
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c083423c1990a410651be44285e63af5
https://doi.org/10.1007/bf00764551
https://doi.org/10.1007/bf00764551
Autor:
J. K. Stubbs, R. M. Acheson
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :899
A number of heterocyclic sulphur compounds and their sulphoxides have been S- and O-alkylated respectively, with silver perchlorate and alkyl halides. 5-Methoxydibenzothiophenium and 10-methoxyphenoxathiinium perchlorates reacted with amines to give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c894b0ca8094a65a0059e5f6aba7928
https://doi.org/10.1039/p19720000899
https://doi.org/10.1039/p19720000899
Autor:
R. M. Acheson, J. K. Stubbs
Publikováno v:
Journal of the Chemical Society C: Organic. :3285
Deuterium labelling experiments have shown that the thermal conversion of tetramethyl 4aH-benzo[c]quinolizine-1,2,3,4-tetracarboxylate into the 1H-isomer is an intramolecular process, whereas the photochemical conversion in methanol involves deuteriu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ddd5b712afa2554a6f5fd8206250d97
https://doi.org/10.1039/j39710003285
https://doi.org/10.1039/j39710003285