名称:
Investigation into the preferred conformation of gabapentin for interaction with its binding site on the α2δ subunit of a calcium channel
摘要:
A series of conformationally restricted Gabapentin analogues has been synthesised and used to propose the preferred conformation of Gabapentin for it to bind to the alpha(2) delta subunit of a calcium channel. (C) 1997 Elsevier Science Ltd.
DOI:
10.1016/s0960-894x(97)10002-6