Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Norbert Gruenfeld"'
Autor:
Frank H. Ebetino, Norbert Gruenfeld, Leslie J. Browne, Candido Gude, Charles F. Huebner, Andrew M. Yuan, James L. Stanton
Publikováno v:
Journal of Medicinal Chemistry. 26:1277-1282
The preparation of a series of 1-glutarylindoline-2(S)-carboxylic acid derivatives, 6a-v and 21a-c, is described. The above compounds were tested for inhibition of angiotensin converting enzyme. The structure-activity relationship of the series is al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::788692a8fd5f69e3666a227eb18c787e
https://doi.org/10.1021/jm00363a012
https://doi.org/10.1021/jm00363a012
Autor:
Joseph F Weidenheimer, William Charles Barringer, Norbert Gruenfeld, George M. Sieger, Francis M. Callahan
Publikováno v:
Journal of Pharmaceutical Sciences. 50:869-874
A series of Mannich base derivatives of N-(2-thiazolyl)-1-phenol-4-sulfonamide has been synthesized and characterized largely in the form of hydrochloride salts and acetyl derivatives. The results on a variety of biological screening tests carried ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7edfcbbdf28503b76bc9e70a32de431
https://doi.org/10.1002/jps.2600501017
https://doi.org/10.1002/jps.2600501017
Autor:
S. Morris Kupchan, Norbert Gruenfeld
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 48:727-730
Cryptenamine has been reported to have a more favorable ratio of emetic to hpotensive dose than other veratrum preparations, and the advantageous ratio has geen attributed to the presence of new hypotensive alkaloids. Cryptenamine was fractionated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9216d069122796a7a6530d47ec58115d
https://doi.org/10.1002/jps.3030481208
https://doi.org/10.1002/jps.3030481208
Autor:
S. Morris Kupchan, Norbert Gruenfeld
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 48:737-739
The structure of germbudine has been elucidated as germine 3- d-threo -2′,3′-dihydroxy-2′-methylbutyrate 15- l -2 methylbutyrate (V). Oxidation of germbudine with periodic acid and subsequent alkaline hydrolysis afforded germine 15- l -2′-met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bff607b491ca2061334612cf58cb9d17
https://doi.org/10.1002/jps.3030481211
https://doi.org/10.1002/jps.3030481211
Autor:
William Macchia, Robert C. Friedmann, Norbert Gruenfeld, Michael H. Ackerman, Joseph E. Babiarz, Andrew M. Yuan, James L. Stanton
Publikováno v:
Chemischer Informationsdienst. 15
The synthesis of N-(3-mercaptopropionyl)-N-arylglycines (14a-x),- N-arylalanines (15a,b),-N-cycloalkylglycines (16a-k), and -1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids (17a-d), -1,2,3,4-tetrahydroquinoline-2-carboxylic acids (18a-f), and -indo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dd79ce76b95842594628bd26a9e671f
https://doi.org/10.1002/chin.198406172
https://doi.org/10.1002/chin.198406172
Autor:
Sam J. Piliero, Louis J. Ignarro, Norbert Gruenfeld, Jan W. F. Wasley, Doebel Karl J, Mary Lee Graeme
Publisher Summary This chapter elaborates studies analyzing non-steroidal anti-inflammatory agents. The importance of the circulating lymphocyte in association with the auto-immune component of adjuvant disease was shown by studies with heterologous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecefa38619d456fea37d360f7657f084
https://doi.org/10.1016/s0065-7743(08)60659-4
https://doi.org/10.1016/s0065-7743(08)60659-4
Autor:
Doebel Karl J, Sam J. Piliero, Mary Lee Graeme, Louis J. Ignarro, Jan W. F. Wasley, Norbert Gruenfeld
Publisher Summary This chapter elaborates the development and clinical studies of nonsteroidal anti-inflammatory agents. The studies of the possible role of infectious inductions and/or adverse immunological reactions continue with the hope of defini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::466910f0f8accd18e13e59374a745210
https://doi.org/10.1016/s0065-7743(08)60343-7
https://doi.org/10.1016/s0065-7743(08)60343-7