Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jacquelyn Lyons"'
Autor:
Thao Ung, Ronald Robinson, Chrysanthe Spais, Justin Schreiber, Hussein Hallak, Jean Husten, Thelma S. Angeles, Jacquelyn Lyons, Yun Liu
Publikováno v:
Bioanalysis. 13:575-585
Aim: To quantify the free form of a protein as a target-engagement biomarker in nonhuman primate serum, a Meso Scale Discovery ligand-binding assay was developed and qualified. Results: The initial assay produced an unexpected artifact when used to m
Autor:
Danyal Butt, Jacquelyn Lyons, Matthew Pollard, Anthony Gerard Doyle, Chen Tian, Doris Shim, Jean Husten, David Mabon, Lynn Dorothy Poulton, Adam Clarke, Vanya Pande
Publikováno v:
mAbs
TL1A is an attractive therapeutic target for the treatment of mucosal inflammation associated with inflammatory bowel disease (IBD) and asthma. Blockade of the TL1A pathway has been shown to reduce inflammatory responses while leaving baseline immuni
Autor:
Mark, Liddament, Jean, Husten, Tanya, Estephan, David, Laine, David, Mabon, Laurie, Pukac, Jacquelyn, Lyons, Adam W, Clarke, Anthony, Doyle
Publikováno v:
Allergy, Asthma & Immunology Research
Reslizumab and mepolizumab are recently approved monoclonal antibodies for the treatment of severe (uncontrolled) eosinophilic asthma. Both are effective in neutralizing the function of interleukin-5 (IL-5). This study is the first to compare the bin
Autor:
Laurie Pukac, Anthony Gerard Doyle, Jacquelyn Lyons, Jean Husten, David Mabon, Adam Clarke, Mark T. Liddament, Tanya Estephan, David Jose Simon Laine
Publikováno v:
Allergy, Asthma & Immunology Research. 11:291
Reslizumab and mepolizumab are recently approved monoclonal antibodies for the treatment of severe (uncontrolled) eosinophilic asthma. Both are effective in neutralizing the function of interleukin-5 (IL-5). This study is the first to compare the bin
Autor:
Ming, Tao, Lisa D, Aimone, Zeqi, Huang, Joanne, Mathiasen, Rita, Raddatz, Jacquelyn, Lyons, Robert L, Hudkins
Publikováno v:
Journal of medicinal chemistry. 55(1)
Previous studies have shown that (5-{4-[3-(R)-2-methylpyrrolin-1-yl-propoxy]phenyl}-2H-pyridazin-3-one) 2 had high affinity for both the human (hH(3)R K(i) = 2.8 nM) and rat H(3)Rs (rH(3)R K(i) = 8.5 nM) but displayed low oral bioavailability in the
Autor:
Robert L, Hudkins, Lisa D, Aimone, Thomas R, Bailey, Robert J, Bendesky, Reddeppa Reddy, Dandu, Derek, Dunn, John A, Gruner, Kurt A, Josef, Yin-Guo, Lin, Jacquelyn, Lyons, Val R, Marcy, Joanne R, Mathiasen, Babu G, Sundar, Ming, Tao, Allison L, Zulli, Rita, Raddatz, Edward R, Bacon
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(18)
H(3)R structure-activity relationships on a novel class of pyridazin-3-one H(3)R antagonists/inverse agonists are disclosed. Modifications of the pyridazinone core, central phenyl ring and linker led to the identification of molecules with excellent
Autor:
Babu G, Sundar, Thomas, Bailey, Edward, Bacon, Lisa, Aimone, Zeqi, Huang, Jacquelyn, Lyons, Rita, Raddatz, Robert, Hudkins
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(18)
Pyridazinone 1 was recently reported as a potent H(3)R antagonist with good drug-like properties and in vivo activity. A series of constrained amine analogs of 1 was synthesized to identify compounds with improved pharmacokinetic profiles. From these
Autor:
Ming Tao, Lisa D. Aimone, Zeqi Huang, Joanne Mathiasen, Rita Raddatz, Jacquelyn Lyons, Robert L. Hudkins
Publikováno v:
Journal of Medicinal Chemistry; Jan2012, Vol. 55 Issue 1, p414-423, 10p