A series of unsymmetrically substituted biphenyl compounds was designed as alpha helical proteomimetics with the aim of inhibiting the binding of coactivator proteins to the nuclear hormone receptor coactivator binding domain. These compounds were synthes
Weiser, Patrick T.,Chang, Ching-Yi,McDonnell, Donald P.,Hanson, Robert N.
p. 917 - 926
(2014/01/23)
More Articles about upstream products of 1542755-53-2