The effects of six imidazole compounds were examined on thromboxane B2 (TxB2) and prostaglandin E2 (PGE2) production and mitogen‐stimulated lymphocyte transformation in human blood mononuclear cells
UK 37248 (4‐(2‐[IH‐imidazol‐l‐yl]ethoxy)benzoic acid), imidazole and 1‐methylimidazole selectively inhibited TxB2 synthesis in a dose‐related manner, with corresponding increases in PGE2 production
Clotrimazole, benzimidazole and 2‐methylimidazole preferentially inhibited TxB synthesis but had little effect on PGE2 production
Clotrimazole and benzimidazole inhibited proliferative responses of the lymphocytes, but UK 37248 and 1‐methylimidazole did not affect transformation at concentrations which inhibited TxB2 synthesis to a similar level (over 90%)
The results do not support involvement of endogenous TxB2 in the process of lymphocyte mitogenesis or in the mechanism of the suppressive effects of some TxB2 synthetase inhibitors.