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2,4-Disubstituted oxazoles and thiazoles as latent pharmacophores for diacylhydrazine of SC-51089, a potent PGE2 antagonist.

Authors :
Hallinan EA
Hagen TJ
Tsymbalov S
Stapelfeld A
Savage MA
Source :
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2001 Jan; Vol. 9 (1), pp. 1-6.
Publication Year :
2001

Abstract

8-Chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(4-pyridinyl)propyl]hydrazide, monohydrochloride (1, SC-51089) is a functional PGE2 antagonist selective for the EP1 receptor subtype with antinociceptive activity. Analogues of SC-51089, in which the diacylhydrazine moiety has been replaced with 2,4-disubstituted-oxazoles and-thiazoles, are described.

Details

Language :
English
ISSN :
0968-0896
Volume :
9
Issue :
1
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry
Publication Type :
Academic Journal
Accession number :
11197330
Full Text :
https://doi.org/10.1016/s0968-0896(00)00229-7