Nalmefene hydrochloride

Applications：Guvacine Hydrochloride is a GABA uptake inhibitor (hGABA T-1, rGABA T-2, hGABA T-3 and hBGT-1) (1,2,3). Gamma-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain (4). Guvacine Hydrochloride may be

Species : Human Assay Principle : Quantitative Target Name : neuronal apoptosis inhibitory protein Sensitivity : 14 pg/ml Detection Range : 35 pg/ml -2000pg/ml

Application Isoguvacine hydrochloride has been used as a &#947-aminobutyric acid type A (GABA A ) receptor agonist: to study its effects on neuronal activity in rats to study its antiallodynic effect in rats to study its effects on baroreflex

Application Isoguvacine hydrochloride has been used as a &#947-aminobutyric acid type A (GABA A ) receptor agonist: to study its effects on neuronal activity in rats to study its antiallodynic effect in rats to study its effects on baroreflex

Application：L-655,708 has been used as an α5 GABAA receptor inverse agonist to inhibit the discriminative stimulus of propofol in a dose-dependent manner.

Application：L-655,708 has been used as an α5 GABAA receptor inverse agonist to inhibit the discriminative stimulus of propofol in a dose-dependent manner.

Application：L-655,708 has been used as an α5 GABAA receptor inverse agonist to inhibit the discriminative stimulus of propofol in a dose-dependent manner.

Application：L-655,708 has been used as an α5 GABAA receptor inverse agonist to inhibit the discriminative stimulus of propofol in a dose-dependent manner.

Application：L-655,708 has been used as an α5 GABAA receptor inverse agonist to inhibit the discriminative stimulus of propofol in a dose-dependent manner.

LEI-401 is a first-in-class, selective, and CNS-active NAPE-PLD (N-acylphosphatidylethanolamine phospholipase D) inhibitor, with an IC 50 of 27 nM. LEI-401 modulates emotional behavior in mice.In VitroLEI-401 reduced a broad range of NAEs including

An endocannabinoid that contains linoleate in place of the arachidonate moiety of AEA has been detected in porcine brain and murine peritoneal macrophages and has weak affinity for the CB1 and CB2 receptors (Kis =10 &microM and 25 &microM,

MDL 105519 is a potent and selective antagonist of glycine binding to the NMDA receptor.In VitroMDL 105519 is a potent and selective ligand for the glycine recognition site that completely inhibit the binding of [ 3 H]glycine to rat brain membranes