Zobrazeno 1 - 9
of 9
pro vyhledávání: '"J. M. Hinkley"'
Autor:
T. E. Mertz, Leslie M. Werbel, C. S. Stratton, S. Hastings, Milton L. Hoefle, T. J. Steffe, J. M. Hinkley, L. T. Blouin, R. W. Fleming
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::069e74016ff4a2186eb79c3c14db5d81
https://doi.org/10.1002/chin.199122152
https://doi.org/10.1002/chin.199122152
Autor:
Leslie M. Werbel, T. E. Mertz, C. S. Stratton, R. W. Fleming, T. J. Steffe, Stephen G. Hastings, L. T. Blouin, Milton L. Hoefle, J. M. Hinkley
Publikováno v:
Journal of medicinal chemistry. 34(1)
A series of alpha-[(diarylmethoxy)methyl]-1-piperidineethanols was evaluated for antiarrhythmic activity in the coronary artery ligated dog model. Structure-activity relationship studies indicated that the 2,6-dimethylpiperidine group afforded the be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf2380bf40f1b914b1bfd0dfb905b675
https://pubmed.ncbi.nlm.nih.gov/1992154
https://pubmed.ncbi.nlm.nih.gov/1992154
Autor:
Milton L. Hoefle, R. W. Fleming, C. S. Stratton, T. E. Mertz, Stephen G. Hastings, T. J. Steffe, J. M. Hinkley, L. T. Blouin
Publikováno v:
Journal of medicinal chemistry. 34(1)
A series of alpha,alpha-diaryl-1-piperidinebutanols was evaluated for antiarrhythmic activity in the coronary ligated dog model. Structure-activity relationship studies indicated that the 2,6-dimethylpiperidine group yielded compounds with the best a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::323324628858f116ba17616191eeccb8
https://pubmed.ncbi.nlm.nih.gov/1992110
https://pubmed.ncbi.nlm.nih.gov/1992110
Autor:
M. L. Hoefle, Holmes A, I. Nordin, J. M. Hinkley, R. W. Fleming, A. E. Werner, Cohen Dm, Essenburg Ad, Klutchko S, Blankley Cj
Publikováno v:
Journal of Medicinal Chemistry. 29:1953-1961
The synthesis and angiotensin converting enzyme (ACE) inhibiting activities of quinapril (CI-906, 22), its active diacid (CI-928, 33), and its dimethoxy analogue (CI-925, 25) are reported. These tetrahydro-3-isoquinolinecarboxylic acid derivatives po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e01c041adb89cb9f50b460a4a0009b5
https://doi.org/10.1021/jm00160a026
https://doi.org/10.1021/jm00160a026
Autor:
G. B. Trimitsis, J. M. Hinkley, R. TenBrink, A. L. Faburada, R. Anderson, M. Poli, B. Christian, G. Gustafson, J. Erdman, D. Rop
Publikováno v:
The Journal of Organic Chemistry. 48:2957-2962
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e6383486eaa5014453fad1ee414a796
https://doi.org/10.1021/jo00166a004
https://doi.org/10.1021/jo00166a004
Publikováno v:
Journal of the American Chemical Society. 99:4838-4840
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90bca7a10ebab424a931215625f63b7d
https://doi.org/10.1021/ja00456a058
https://doi.org/10.1021/ja00456a058
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d969068fc9ee9469b40ccf8f26493b88
https://doi.org/10.1002/chin.197742118
https://doi.org/10.1002/chin.197742118
Autor:
I. Nordin, R. W. Fleming, Cohen Dm, C. J. Blankley, Sylvester Klutchko, H. R. Kaplan, J. M. Hinkley, Ann Holmes, A. D. Essenburg, A. E. Werner, Milton L. Hoefle
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82af4c43e2bc8b1ecf4dbf6c2cdde880
https://doi.org/10.1002/chin.198711185
https://doi.org/10.1002/chin.198711185
Autor:
R. Anderson, B. Christian, D. Rop, R. Tenbrink, G. B. Trimitsis, J. Erdman, G. Gustafson, A. L. Faburada, M. Poli, J. M. Hinkley
Publikováno v:
Chemischer Informationsdienst. 15
Etude de l'alkylation par des halogenures d'alkyle primaires et secondaires des dianones des phenyl-1, diphenyl-1,1- et methoxy-4'phenyl-1 acetones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0779a18b8c46802853fef092d6891f67
https://doi.org/10.1002/chin.198408134
https://doi.org/10.1002/chin.198408134