Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kevin, Tays"'
Autor:
Zhao Bao-Ping, Kevin Tays, Brad M. Savall, Hui Cai, Michael David Gaul, James P. Edwards, Patricia McGovern, Robin L. Thurmond, Steven P. Meduna
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 25:956-959
Previously disclosed H 4 receptor modulators, the triamino substituted pyridines and pyrimidines, contain a free primary amino (–NH 2 ) group. In this Letter we demonstrate that an exocyclic amine (NH 2 ) is not needed to maintain affinity, and als
Autor:
Michael D. Hack, Brad M. Savall, Kevin Tays, Paul J. Dunford, Jeffery M. Cowden, Ronald L. Wolin, James P. Edwards, Frank Chavez, Robin L. Thurmond
Publikováno v:
Journal of Medicinal Chemistry. 57:2429-2439
This report discloses the discovery and SAR of a series of 6-alkyl-2-aminopyrimidine derived histamine H4 antagonists that led to the development of JNJ 39758979, which has been studied in phase II clinical trials in asthma and atopic dermatitis. Bui
Autor:
Brad M, Savall, Frank, Chavez, Kevin, Tays, Paul J, Dunford, Jeffery M, Cowden, Michael D, Hack, Ronald L, Wolin, Robin L, Thurmond, James P, Edwards
Publikováno v:
Journal of medicinal chemistry. 57(6)
This report discloses the discovery and SAR of a series of 6-alkyl-2-aminopyrimidine derived histamine H4 antagonists that led to the development of JNJ 39758979, which has been studied in phase II clinical trials in asthma and atopic dermatitis. Bui
Autor:
Kevin Tays, Jeffrey Atkinson
Publikováno v:
Scopus-Elsevier
The boron trichloride sensitive methoxymethyl (MOM) protecting group has been used to efficiently synthesize polymethoxylated derivatives of the benzoxazinone family of cyclic hydroxamic acids. The MOM group allows the unveiling of the hemiacetal at
Autor:
Kevin Tays, Jeffrey Atkinson
Publikováno v:
ChemInform. 29
The boron trichloride sensitive methoxymethyl (MOM) protecting group has been used to efficiently synthesize polymethoxylated derivatives of the benzoxazinone family of cyclic hydroxamic acids. The MOM group allows the unveiling of the hemiacetal at