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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
Harvard
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/jm4006466APA
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/jm4006466Vancouver
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/jm4006466Author
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.
Bibtex
@article{02491cc0e1dc43dfa12b63481b17082b,
title = "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",
author = "Jacob Krall and Jensen, {Claus Hatt} and S{\o}rensen, {Troels Ersted} and Birgitte Nielsen and Jensen, {Anders A.} and Tommy Sander and Thomas Balle and Bente Fr{\o}lund",
year = "2013",
month = jul,
day = "15",
doi = "10.1021/jm4006466",
language = "English",
volume = "56",
pages = "6536−6540",
journal = "Journal of Medicinal Chemistry",
issn = "0022-2623",
publisher = "American Chemical Society",
number = "16",
}
RIS
TY - JOUR
T1 - 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
T2 - design, synthesis, and pharmacological evaluation
AU - Krall, Jacob
AU - Jensen, Claus Hatt
AU - Sørensen, Troels Ersted
AU - Nielsen, Birgitte
AU - Jensen, Anders A.
AU - Sander, Tommy
AU - Balle, Thomas
AU - Frølund, Bente
PY - 2013/7/15
Y1 - 2013/7/15
U2 - 10.1021/jm4006466
DO - 10.1021/jm4006466
M3 - Journal article
C2 - 23855889
VL - 56
SP - 6536−6540
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
SN - 0022-2623
IS - 16
ER -
