R 68 070: Thromboxane A2 Synthetase Inhibition and Thromboxane A2/Prostaglandin Endoperoxide Receptor Blockade Combined in One Molecule - I. Biochemical Profile In Vitro

F De Clerck; J Beetens; D de Chaffoy de Courcelles; E Freyne; P A J Janssen

doi:10.1055/s-0038-1646523

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 1989; 61(01): 035-042
DOI: 10.1055/s-0038-1646523

Original Article

Schattauer GmbH Stuttgart

R 68 070: Thromboxane A₂ Synthetase Inhibition and Thromboxane A₂/Prostaglandin Endoperoxide Receptor Blockade Combined in One Molecule - I. Biochemical Profile In Vitro

Authors

F De Clerck

The Department of Haematology, Janssen Research Foundation, Beerse, Belgium
J Beetens

The Department of Haematology, Janssen Research Foundation, Beerse, Belgium
D de Chaffoy de Courcelles

¹The Department of Biochemistry, Janssen Research Foundation, Beerse, Belgium
E Freyne

²The Department of Chemistry, Janssen Research Foundation, Beerse, Belgium
P A J Janssen

The Department of Haematology, Janssen Research Foundation, Beerse, Belgium

Abstract

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Summary

R 68 070 or (E)-5-[[[(3-pyridinyl)[3-(trifluoromethyl)phenyl]- methylen]amino]oxy] pentanoic acid (Janssen Research Foundation, Belgium) combines specific thromboxane A₂ (TXA₂) synthetase inhibition with TXA₂/prostaglandin endoperoxide receptor blockade in one molecule.

In vitro, the compound specifically inhibits the production of TXB₂ from [¹⁴C] arachidonic acid by washed human platelets (IC₅₀ = 8.2 × 10^-9 M) and by platelet microsomes (IC₅₀ = 3.6 × 10^-9 M), of MDA (IC₅₀ = 1.91 × 10^-8 M) and of TXB₂ (IC₅₀ = 1.47 × 10^-8 M) by thrombin-coagulated human platelet-rich plasma (P.R.P.) and whole blood respectively and increases the levels of PGD₂, PGE₂, PGF_2α and 6-keto-PGF_1α. The activity of cyclo-oxygenase-, prostacyclin synthetase-, 5-, 12- and 15-lipoxygenase-enzymes are not affected. Additionally, R 68 070 inhibits human platelet aggregation in P.R.P. induced by U 46619 3 × 10^-7 M to 2 × 10^-6 M (IC₅₀ = 2.08 × 10^-6 M to 2.66 × 10^-5 M), collagen 0.5 to 2 μg/ml (IC₅₀ = 2.85 × 10^-6 M to 4.81 × 10^-5 M), arachidonic acid 7.5 × 10^-4 M to 2 × 10^- M (IC₅₀ = 2.1 × 10^-8 M to 3.3 × 10^-8 M) and the U 46619 (1 × 10^-7 M)-induced accumulation of [32P] phosphatidic acid (IC₅₀ = 5.24 × 10^-7 M) in washed human platelets. Collagen (0.75 μg/ml)-induced ATP release (IC₅₀ = 4.1 × 10^-6 M), ADP (1 to 2.5 × 10^-6 M)-induced second wave aggregation (IC₅₀ = 3.19 × 10^-6 M) in P.R.P. as well as the collagen (1 μg/ml)-induced adhesion/aggregation reaction in human whole blood (IC₅₀ = 1.02 × 10^-5 M) are reduced as well by the compoun.

Primary platelet reactions induced by serotonin, ADP, PAF, or A 23187, platelet adenylate cyclase- and cAMP phosphodiesterase-activity, and platelet inhibitory activities of PGD₂, PGI₂, PGE₂, PGE₁ are not modified by R 68 070.

This biochemical profile is compatible with a dual mechanism of action of R 68 070, namely TXA₂ synthetase inhibition at low concentrations, plus additionally TXA₂/prostaglandin endoperoxide receptor blockade at higher concentrations

Key words

R 68 070 - TXA₂-synthetase - Receptor blockade - Man - Experimental models

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References

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