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

Research output: Contribution to journalJournal articleResearchpeer-review

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 journalJournal articleResearchpeer-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.2018.08.094

APA

Alessandro, G., Krall, J., Nielsen, B., Sørensen, T. E., Kongstad, K. T., Barbara, R., ... 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.2018.08.094

Vancouver

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.2018.08.094

Author

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 = "10",
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

VL - 158

SP - 311

EP - 321

JO - European Journal of Medicinal Chemistry

JF - European Journal of Medicinal Chemistry

SN - 0223-5234

ER -

ID: 203013437