Standard
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site. / Alessandro, Giraudo; Krall, Jacob; Nielsen, Birgitte; Sørensen, Troels Ersted; Kongstad, Kenneth Thermann; Barbara, Rolando; Donatella, Boschi; Frølund, Bente; Lolli, Marco L.
In:
European Journal of Medicinal Chemistry, Vol. 158, 05.10.2018, p. 311-321.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Alessandro, G, Krall, J
, Nielsen, B, Sørensen, TE
, Kongstad, KT, Barbara, R, Donatella, B
, Frølund, B & Lolli, ML 2018, '
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site',
European Journal of Medicinal Chemistry, vol. 158, pp. 311-321.
https://doi.org/10.1016/j.ejmech.2018.08.094APA
Alessandro, G., Krall, J.
, Nielsen, B., Sørensen, T. E.
, Kongstad, K. T., Barbara, R., Donatella, B.
, Frølund, B., & Lolli, M. L. (2018).
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site.
European Journal of Medicinal Chemistry,
158, 311-321.
https://doi.org/10.1016/j.ejmech.2018.08.094Vancouver
Alessandro G, Krall J
, Nielsen B, Sørensen TE
, Kongstad KT, Barbara R et al.
4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site.
European Journal of Medicinal Chemistry. 2018 Oct 5;158:311-321.
https://doi.org/10.1016/j.ejmech.2018.08.094Author
Alessandro, Giraudo ; Krall, Jacob ; Nielsen, Birgitte ; Sørensen, Troels Ersted ; Kongstad, Kenneth Thermann ; Barbara, Rolando ; Donatella, Boschi ; Frølund, Bente ; Lolli, Marco L. / 4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site. In: European Journal of Medicinal Chemistry. 2018 ; Vol. 158. pp. 311-321.
Bibtex
@article{c9e4c580a7164a0394a6517bb5d2f526,
title = "4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site",
author = "Giraudo Alessandro and Jacob Krall and Birgitte Nielsen and S{\o}rensen, {Troels Ersted} and Kongstad, {Kenneth Thermann} and Rolando Barbara and Boschi Donatella and Bente Fr{\o}lund and Lolli, {Marco L.}",
year = "2018",
month = oct,
day = "5",
doi = "10.1016/j.ejmech.2018.08.094",
language = "English",
volume = "158",
pages = "311--321",
journal = "European Journal of Medicinal Chemistry",
issn = "0223-5234",
publisher = "Elsevier Masson",
}
RIS
TY - JOUR
T1 - 4-Hydroxy-1,2,3-triazole moiety as bioisostere of the carboxylic acid function: a novel scaffold to probe the orthosteric gamma-aminobutyric acid receptor binding site
AU - Alessandro, Giraudo
AU - Krall, Jacob
AU - Nielsen, Birgitte
AU - Sørensen, Troels Ersted
AU - Kongstad, Kenneth Thermann
AU - Barbara, Rolando
AU - Donatella, Boschi
AU - Frølund, Bente
AU - Lolli, Marco L.
PY - 2018/10/5
Y1 - 2018/10/5
U2 - 10.1016/j.ejmech.2018.08.094
DO - 10.1016/j.ejmech.2018.08.094
M3 - Journal article
C2 - 30223119
VL - 158
SP - 311
EP - 321
JO - European Journal of Medicinal Chemistry
JF - European Journal of Medicinal Chemistry
SN - 0223-5234
ER -
