Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Bioorg Med Chem Lett ; 17(20): 5715-9, 2007 Oct 15.
Article in English | MEDLINE | ID: mdl-17766108

ABSTRACT

Furan-containing congeners of the histamine H(2) receptor antagonist ranitidine were synthesized and tested for improgan-like antinociceptive activity. The most potent ligand of the series, VUF5498, is the most potent improgan-like agent described to date (ED(50)=25 nmol, icv). This compound is approximately equal in potency with morphine. These non-imidazole, improgan-like pain relievers further define the structural requirements for analgesics of this class and are important tools for ongoing mechanism-based studies.


Subject(s)
Cimetidine/analogs & derivatives , Furans/chemistry , Nociceptors/metabolism , Ranitidine/chemistry , Ranitidine/pharmacology , Animals , Cimetidine/chemistry , Cimetidine/pharmacology , Male , Molecular Structure , Rats , Rats, Sprague-Dawley , Structure-Activity Relationship
SELECTION OF CITATIONS
SEARCH DETAIL
...