Referenced in: none

Automatically associated channels: TRP , TRPV , TRPV1

Title: Efficient modulation of γ-aminobutyric acid type A receptors by piperine derivatives.

Authors: Angela Schöffmann, Laurin Wimmer, Daria Goldmann, Sophia Khom, Juliane Hintersteiner, Igor Baburin, Thomas Schwarz, Michael Hintersteininger, Peter Pakfeifer, Mouhssin Oufir, Matthias Hamburger, Thomas Erker, Gerhard F Ecker, Marko D Mihovilovic, Steffen Hering

Journal, date & volume: J. Med. Chem., 2014 Jul 10 , 57, 5602-19

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24905252

Abstract
Piperine activates TRPV1 (transient receptor potential vanilloid type 1 receptor) receptors and modulates γ-aminobutyric acid type A receptors (GABAAR). We have synthesized a library of 76 piperine analogues and analyzed their effects on GABAAR by means of a two-microelectrode voltage-clamp technique. GABAAR were expressed in Xenopus laevis oocytes. Structure-activity relationships (SARs) were established to identify structural elements essential for efficiency and potency. Efficiency of piperine derivatives was significantly increased by exchanging the piperidine moiety with either N,N-dipropyl, N,N-diisopropyl, N,N-dibutyl, p-methylpiperidine, or N,N-bis(trifluoroethyl) groups. Potency was enhanced by replacing the piperidine moiety by N,N-dibutyl, N,N-diisobutyl, or N,N-bistrifluoroethyl groups. Linker modifications did not substantially enhance the effect on GABAAR. Compound 23 [(2E,4E)-5-(1,3-benzodioxol-5-yl)-N,N-dipropyl-2,4-pentadienamide] induced the strongest modulation of GABAA (maximal GABA-induced chloride current modulation (IGABA-max = 1673% ± 146%, EC50 = 51.7 ± 9.5 μM), while 25 [(2E,4E)-5-(1,3-benzodioxol-5-yl)-N,N-dibutyl-2,4-pentadienamide] displayed the highest potency (EC50 = 13.8 ± 1.8 μM, IGABA-max = 760% ± 47%). Compound 23 induced significantly stronger anxiolysis in mice than piperine and thus may serve as a starting point for developing novel GABAAR modulators.