Title : Prostaglandin H synthase and lipoxygenase mediated activation of xenobiotics in platelets.

Pub. Date : 1999

PMID : 10667392






9 Functional Relationships(s)
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1 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. Aspirin pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
2 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. Aspirin pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
3 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. Indomethacin pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
4 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. Indomethacin pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
5 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. 1-naphthol pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
6 Pretreatment by two inhibitors of PHS, aspirin and indomethacin, resulted in a dose-dependent inhibition of alpha-naphthol-induced covalent binding, confirming PHS involvement. 1-naphthol pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
7 Furthermore, combined treatment of aspirin and NDGA almost abolished the increase of alpha-naphthol-induced covalent binding, suggesting that PHS and LPO are both major pathways for xenobiotic activation in platelets. Aspirin pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
8 Furthermore, combined treatment of aspirin and NDGA almost abolished the increase of alpha-naphthol-induced covalent binding, suggesting that PHS and LPO are both major pathways for xenobiotic activation in platelets. Masoprocol pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens
9 Furthermore, combined treatment of aspirin and NDGA almost abolished the increase of alpha-naphthol-induced covalent binding, suggesting that PHS and LPO are both major pathways for xenobiotic activation in platelets. 1-naphthol pterin-4 alpha-carbinolamine dehydratase 1 Homo sapiens