7-(1,1-Dimethylethyl)-6-(2-ethyl-2 <i>H</i> -1,2,4- triazol-3-ylmethoxy)-3-(2-fluorophenyl)- 1,2,4-triazolo[4,3- <i>b</i> ]pyridazine:  A Functionally Selective γ-Aminobutyric Acid <sub>A</sub> (GABA <sub>A</sub> ) α2/α3-Subtype Selective Agonist That Exhibits Potent Anxiolytic Activity but Is Not Sedating in Animal Models

Robert W. Carling, Andrew Madin, Alec Guiblin, Michael G. N. Russell, Kevin W. Moore, Andrew Mitchinson, Bindi Sohal, Andrew Pike, Susan M. Cook, Ian Ragan,

Journal of Medicinal Chemistry · 2005 · 54 citations · 21 references

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Abstract

There is increasing evidence that compounds with selectivity for gamma-aminobutyric acid(A) (GABA(A)) alpha2- and/or alpha3-subtypes may retain the desirable anxiolytic activity of nonselective benzodiazepines but possess an improved side effect profile. Herein we describe a novel series of GABA(A) alpha2/alpha3 subtype-selective agonists leading to the identification of the development candidate 17, a nonsedating anxiolytic in preclinical animal assays.

References

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