Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mary K. Peters"'
Autor:
Sha Liu, Raymond F. Kauffman, Garret J. Etgen, Dale E. Mais, Allie Edward Tripp, Chahrzad Montrose-Rafizadeh, Yanping Xu, Leonard L. Winneroski, Brian A. Oldham, Patric James Hahn, Deepa Rungta, Dawn A. Brooks, William R. Bensch, Mary K. Peters, Sarah B. Wilson, Kathy M Ogilvie, Mccarthy James R, Jacob R Bosley, Samuel J. Dominianni, Christopher John Rito, Richard W. Zink, Robert J. Ardecky, James S. Bean, Anthony J. Shuker, Carol L. Broderick, Gregory A. Stephenson
Publikováno v:
Journal of Medicinal Chemistry. 47:2422-2425
The design and synthesis of the dual peroxisome proliferator activated receptor (PPAR) alpha/gamma agonist (S)-2-methyl-3-[4-[2-(5-methyl-2-thiophen-2-yl-oxazol-4-yl)ethoxy]phenyl]-2-phenoxypropionic acid (2) for the treatment of type 2 diabetes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1308bb3472bf950182ed5ac246acab95
https://doi.org/10.1021/jm0342616
https://doi.org/10.1021/jm0342616
Autor:
Yanping Xu, Mary K. Peters, Brian A. Oldham, Sarah B. Wilson, Aaron Kunkel, Allie Edward Tripp, Minmin Wang, Robert E. Babine, Leonard L. Winneroski, Richard W. Zink, Robert J. Ardecky, Deepa K. Rungta, Mccarthy James R, Garret J. Etgen, Christopher John Rito, D. R. Hutchison, Dawn A. Brooks, Dale E. Mais, Raymond F. Kauffman, Kathleen M. Ogilvie, Chahrzad Montrose-Rafizadeh
Publikováno v:
Bioorganicmedicinal chemistry letters. 14(24)
To understand the species selectivity in a series of alpha-methyl-alpha-phenoxy carboxylic acid PPARalpha/gamma dual agonists (1-11), structure-based molecular modeling was carried out in the ligand binding pockets of both human and mouse PPARalpha.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::538c575e3eaee66c93b66cea90fda590
https://pubmed.ncbi.nlm.nih.gov/15546740
https://pubmed.ncbi.nlm.nih.gov/15546740
Autor:
Andrew Pike, Charles David Jones, Larry John Black, Allen R. Thompson, James A. Clemens, Mary K. Peters, Julie F. Falcone, Mary G. Jevnikar
Publikováno v:
Journal of Medicinal Chemistry. 27:1057-1066
In an effort to prepare nonsteroidal antiestrogens demonstrating greater antagonism and less intrinsic estrogenicity than those currently available, a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives was synthesized. These compounds were prepare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3861982acfe6aaabc912a7d59c53df
https://doi.org/10.1021/jm00374a021
https://doi.org/10.1021/jm00374a021
Autor:
C. D. Jones, Mary K. Peters, L. J. Black, A. J. Pike, M. G. Jevnikar, A. R. Thompson, James A. Clemens, Julie F. Falcone
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9922d380bf463a15066f613ac4391304
https://doi.org/10.1002/chin.198503198
https://doi.org/10.1002/chin.198503198