Standard
4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists. / Receveur, Jean-Marie; Bjurling, Emelie; Ulven, Trond; Little, Paul Brian; Nørregaard, Pia K; Högberg, Thomas.
In:
Bioorganic & Medicinal Chemistry Letters, Vol. 14, No. 20, 18.10.2004, p. 5075-5080.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Receveur, J-M, Bjurling, E
, Ulven, T, Little, PB, Nørregaard, PK & Högberg, T 2004, '
4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists',
Bioorganic & Medicinal Chemistry Letters, vol. 14, no. 20, pp. 5075-5080.
https://doi.org/10.1016/j.bmcl.2004.07.077APA
Receveur, J-M., Bjurling, E.
, Ulven, T., Little, P. B., Nørregaard, P. K., & Högberg, T. (2004).
4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists.
Bioorganic & Medicinal Chemistry Letters,
14(20), 5075-5080.
https://doi.org/10.1016/j.bmcl.2004.07.077Vancouver
Receveur J-M, Bjurling E
, Ulven T, Little PB, Nørregaard PK, Högberg T.
4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists.
Bioorganic & Medicinal Chemistry Letters. 2004 Oct 18;14(20):5075-5080.
https://doi.org/10.1016/j.bmcl.2004.07.077Author
Receveur, Jean-Marie ; Bjurling, Emelie ; Ulven, Trond ; Little, Paul Brian ; Nørregaard, Pia K ; Högberg, Thomas. / 4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists. In: Bioorganic & Medicinal Chemistry Letters. 2004 ; Vol. 14, No. 20. pp. 5075-5080.
Bibtex
@article{282902067a314b6c8e899c1343ac7fb5,
title = "4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists",
abstract = "Synthesis, in vitro biological evaluation and structure-activity relationships of 4-acylamino-and 4-ureidobenzamides as novel hMCH1R-antagonists are disclosed. The nature of the amine side chains could be varied considerably in contrast to the central benzamide scaffold and aromatic substituents.",
keywords = "Animals, Benzamides, CHO Cells, Cricetinae, Cricetulus, Humans, Hypothalamic Hormones, Ligands, Melanins, Pituitary Hormones, Radioligand Assay, Receptors, Pituitary Hormone, Structure-Activity Relationship, Urea",
author = "Jean-Marie Receveur and Emelie Bjurling and Trond Ulven and Little, {Paul Brian} and N{\o}rregaard, {Pia K} and Thomas H{\"o}gberg",
year = "2004",
month = oct,
day = "18",
doi = "10.1016/j.bmcl.2004.07.077",
language = "English",
volume = "14",
pages = "5075--5080",
journal = "Bioorganic & Medicinal Chemistry Letters",
issn = "0960-894X",
publisher = "Pergamon Press",
number = "20",
}
RIS
TY - JOUR
T1 - 4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists
AU - Receveur, Jean-Marie
AU - Bjurling, Emelie
AU - Ulven, Trond
AU - Little, Paul Brian
AU - Nørregaard, Pia K
AU - Högberg, Thomas
PY - 2004/10/18
Y1 - 2004/10/18
N2 - Synthesis, in vitro biological evaluation and structure-activity relationships of 4-acylamino-and 4-ureidobenzamides as novel hMCH1R-antagonists are disclosed. The nature of the amine side chains could be varied considerably in contrast to the central benzamide scaffold and aromatic substituents.
AB - Synthesis, in vitro biological evaluation and structure-activity relationships of 4-acylamino-and 4-ureidobenzamides as novel hMCH1R-antagonists are disclosed. The nature of the amine side chains could be varied considerably in contrast to the central benzamide scaffold and aromatic substituents.
KW - Animals
KW - Benzamides
KW - CHO Cells
KW - Cricetinae
KW - Cricetulus
KW - Humans
KW - Hypothalamic Hormones
KW - Ligands
KW - Melanins
KW - Pituitary Hormones
KW - Radioligand Assay
KW - Receptors, Pituitary Hormone
KW - Structure-Activity Relationship
KW - Urea
U2 - 10.1016/j.bmcl.2004.07.077
DO - 10.1016/j.bmcl.2004.07.077
M3 - Journal article
VL - 14
SP - 5075
EP - 5080
JO - Bioorganic & Medicinal Chemistry Letters
JF - Bioorganic & Medicinal Chemistry Letters
SN - 0960-894X
IS - 20
ER -
