Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation

Jacob Krall; Claus Hatt Jensen; Troels Ersted Sørensen; Birgitte Nielsen; Anders A. Jensen; Tommy Sander; Thomas Balle; Bente Frølund

doi:10.1021/jm4006466

Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation

Jacob Krall, Claus Hatt Jensen, Troels Ersted Sørensen, Birgitte Nielsen, Anders A. Jensen, Tommy Sander, Thomas Balle, Bente Frølund

Research output: Contribution to journal › Journal article › Research › peer-review

6 Citations (Scopus)

Original language	English
Journal	Journal of Medicinal Chemistry
Volume	56
Issue number	16
Pages (from-to)	6536−6540
Number of pages	5
ISSN	0022-2623
DOIs	https://doi.org/10.1021/jm4006466
Publication status	Published - 15 Jul 2013

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Cite this

Krall, J., Jensen, C. H., Sørensen, T. E., Nielsen, B., Jensen, A. A., Sander, T., Balle, T., & Frølund, B. (2013). Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation. Journal of Medicinal Chemistry, 56(16), 6536−6540. https://doi.org/10.1021/jm4006466

Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted : design, synthesis, and pharmacological evaluation. / Krall, Jacob; Jensen, Claus Hatt; Sørensen, Troels Ersted; Nielsen, Birgitte ; Jensen, Anders A.; Sander, Tommy; Balle, Thomas; Frølund, Bente.

In: Journal of Medicinal Chemistry, Vol. 56, No. 16, 15.07.2013, p. 6536−6540.

Research output: Contribution to journal › Journal article › Research › peer-review

Krall, J, Jensen, CH, Sørensen, TE, Nielsen, B , Jensen, AA, Sander, T, Balle, T & Frølund, B 2013, 'Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation', Journal of Medicinal Chemistry, vol. 56, no. 16, pp. 6536−6540. https://doi.org/10.1021/jm4006466

Krall J, Jensen CH, Sørensen TE, Nielsen B , Jensen AA, Sander T et al. Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted: design, synthesis, and pharmacological evaluation. Journal of Medicinal Chemistry. 2013 Jul 15;56(16):6536−6540. https://doi.org/10.1021/jm4006466

Krall, Jacob ; Jensen, Claus Hatt ; Sørensen, Troels Ersted ; Nielsen, Birgitte ; Jensen, Anders A. ; Sander, Tommy ; Balle, Thomas ; Frølund, Bente. / Exploring the orthosteric binding site of the γ-aminobutyric acid type A receptor using 4-(piperidin-4-yl)-1-hydroxypyrazoles 3- or 5-imidazolyl substituted : design, synthesis, and pharmacological evaluation. In: Journal of Medicinal Chemistry. 2013 ; Vol. 56, No. 16. pp. 6536−6540.

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