4-Acylamino-and 4-ureidobenzamides as melanin-concentrating hormone (MCH) receptor 1 antagonists

Research output: Contribution to journalJournal articleResearchpeer-review

  • Jean-Marie Receveur
  • Emelie Bjurling
  • Ulven, Trond
  • Paul Brian Little
  • Pia K Nørregaard
  • Thomas Högberg
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.
Original languageEnglish
JournalBioorganic & Medicinal Chemistry Letters
Volume14
Issue number20
Pages (from-to)5075-5080
Number of pages6
ISSN0960-894X
DOIs
Publication statusPublished - 18 Oct 2004

    Research areas

  • Animals, Benzamides, CHO Cells, Cricetinae, Cricetulus, Humans, Hypothalamic Hormones, Ligands, Melanins, Pituitary Hormones, Radioligand Assay, Receptors, Pituitary Hormone, Structure-Activity Relationship, Urea

ID: 189159527