Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Andrea H. Ayscue"'
Autor:
Andrea H. Ayscue, Daniel D. Sternbach, Millard H. Lambert, Jennifer S. Smith, Timothy M. Willson, Brad R. Henke, Kelli D. Plunket, Kevin G. Liu, Lisa M. Leesnitzer
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:2385-2388
A series of oxadiazole-substituted α-isopropoxy phenylpropanoic acids with dual agonist activity on PPARα and PPARγ is described. Several of these compounds also showed partial agonist activity on PPARδ. Resolution of one analogue showed that PPA
Autor:
Lisa M. Leesnitzer, Timothy M. Willson, Millard H. Lambert, Daniel D. Sternbach, Brad R. Henke, Kevin G. Liu, Kelli D. Plunket, Andrea H. Ayscue, Jennifer S. Smith
Publikováno v:
ChemInform. 32
A series of oxadiazole-substituted α-isopropoxy phenylpropanoic acids with dual agonist activity on PPARα and PPARγ is described. Several of these compounds also showed partial agonist activity on PPARδ. Resolution of one analogue showed that PPA
Autor:
Andrea H. Ayscue, Brad R. Henke, Daniel D. Sternbach, Lisa M. Leesnitzer, William R. Oliver, Kevin G. Liu, Millard H. Lambert, Kelli D. Plunket, Timothy M. Willson, H. Eric Xu
Publikováno v:
ChemInform. 33
A series of PPARgamma agonists were synthesized from L-tyrosine that incorporated low molecular weight N-substituents. The most potent analogue, pyrrole (4e), demonstrated a K(i) of 6.9nM and an EC(50) of 4.7nM in PPARgamma binding and functional ass
Autor:
Andrea H. Ayscue, Lisa M. Leesnitzer, Jason A. Holt, Shawn P. Williams, Thomas G. Consler, Andrew N. Billin, G. Bruce Wisely
Publikováno v:
Molecular endocrinology (Baltimore, Md.). 17(9)
The ligand-binding domain (LBD) of apo-nuclear receptors in solution is thought to be a very dynamic structure with many possible conformations. Upon ligand binding, the structure is stabilized to a more rigid conformation. The dynamic stabilization
Autor:
Andrea H. Ayscue, Daniel D. Sternbach, H. Eric Xu, Brad R. Henke, Timothy M. Willson, William R. Oliver, Millard H. Lambert, Kelli D. Plunket, Lisa M. Leesnitzer, Kevin G. Liu
Publikováno v:
Bioorganicmedicinal chemistry letters. 11(24)
A series of PPARgamma agonists were synthesized from L-tyrosine that incorporated low molecular weight N-substituents. The most potent analogue, pyrrole (4e), demonstrated a K(i) of 6.9nM and an EC(50) of 4.7nM in PPARgamma binding and functional ass