Structural analogues of the natural products magnolol and honokiol as potent allosteric potentiators of GABAA receptors
作者:Alexander Fuchs、Roland Baur、Clara Schoeder、Erwin Sigel、Christa E. Müller
DOI:10.1016/j.bmc.2014.10.027
日期:2014.12
Biphenylic compounds related to the natural products magnolol and 4'-O-methylhonokiol were synthesized, evaluated and optimized as positive allosteric modulators (PAMs) of GABA(A) receptors. The most efficacious compounds were the magnolol analog 5-ethyl-5'-hexylbiphenyl-2,2'-diol (45) and the honokiol analogs 4'-methoxy-5-propylbiphenyl-2-ol (61), 5-butyl-4'-methoxybiphenyl-2-ol (62) and 5-hexyl-4'- methoxybiphenyl-2-ol (64), which showed a most powerful potentiation of GABA-induced currents (up to 20-fold at a GABA concentration of 3 mu M). They were found not to interfere with the allosteric sites occupied by known allosteric modulators, such as benzodiazepines and N-arachidonoylglycerol. These new PAMs will be useful as pharmacological tools and may have therapeutic potential for mono-therapy, or in combination, for example, with GABA(A) receptor agonists. (C) 2014 Elsevier Ltd. All rights reserved.
Hong, X. J.; Ge, M. J.; Zhao, X. M., Molecular Crystals and Liquid Crystals (1969-1991), 1983, vol. 99, p. 81 - 88
作者:Hong, X. J.、Ge, M. J.、Zhao, X. M.、Fen, Z. R.、Liu, Z. J.