In:
Journal of Pharmacy and Pharmacology, Oxford University Press (OUP), Vol. 53, No. 9 ( 2010-02-18), p. 1295-1302
Abstract:
The effects of 14 synthetic 2′-hydroxychalcone derivatives on prostaglandin E2 (PGE2) production in rat peritoneal macrophages stimulated by the protein kinase C activator, 12-O-tetradecanoylphorbol 13-acetate (TPA), were examined to clarify the structure-activity relationship. 2′,4-Dihydroxy-4′-methoxychalcone (compound 3), 2′,4-dihydroxy-6′-methoxychalcone (compound 8) and 2′-hydroxy-4′-methoxychalcone (compound 9) suppressed PGE2 production more potently than the other compounds. The IC50 (50 % Inhibitory concentration) value for compounds 3, 8 and 9 was calculated to be 3 μ. The activity of cyclooxygenase (COX)-1 was inhibited slightly by compound 9, but that of COX-2 was not inhibited. At concentrations that inhibited the production of PGE2, compound 9 had no effect on the release of radioactivity from [3H]arachidonic acid-labelled macrophages stimulated by TPA. Western-blot analysis revealed that the induction of COX-2 protein by TPA was inhibited by compound 9 in parallel with the inhibition of PGE2 production. Compounds 3 and 8 had similar effects. These findings suggest that 4′-methoxyl and 6′-methoxyl groups are required for the expression of more potent inhibitory activity against PGE2 production, and that the inhibition of PGE2 production by these 2′-hydroxychalcone derivatives is due to the inhibition of TPA-induced COX-2 protein expression.
Type of Medium:
Online Resource
ISSN:
0022-3573
,
2042-7158
DOI:
10.1211/0022357011776595
Language:
English
Publisher:
Oxford University Press (OUP)
Publication Date:
2010
detail.hit.zdb_id:
2041988-0
detail.hit.zdb_id:
2050532-2
SSG:
15,3
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