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169 related items for PubMed ID: 3122826
1. Reductive inactivation of soybean lipoxygenase 1 by catechols: a possible mechanism for regulation of lipoxygenase activity. Kemal C, Louis-Flamberg P, Krupinski-Olsen R, Shorter AL. Biochemistry; 1987 Nov 03; 26(22):7064-72. PubMed ID: 3122826 [Abstract] [Full Text] [Related]
2. Formation of free radical metabolites in the reaction between soybean lipoxygenase and its inhibitors. An ESR study. Van der Zee J, Eling TE, Mason RP. Biochemistry; 1989 Oct 17; 28(21):8363-7. PubMed ID: 2557901 [Abstract] [Full Text] [Related]
3. Interaction of the di-catechols rooperol and nordihydroguaiaretic acid with oxidative systems in the human blood. A structure-activity relationship. Van der Merwe MJ, Jenkins K, Theron E, van der Walt BJ. Biochem Pharmacol; 1993 Jan 26; 45(2):303-11. PubMed ID: 8382058 [Abstract] [Full Text] [Related]
6. Inhibition of arachidonic acid release by nordihydroguaiaretic acid and its antioxidant action in rat alveolar macrophages and Chinese hamster lung fibroblasts. Robison TW, Sevanian A, Forman HJ. Toxicol Appl Pharmacol; 1990 Aug 26; 105(1):113-22. PubMed ID: 2118282 [Abstract] [Full Text] [Related]
7. Effect of a lipoxygenase inhibitor on vasoconstriction in dog lung. el-Kashef HA, Hofman WF, Ehrhart IC. Am J Physiol; 1989 Dec 26; 257(6 Pt 2):H1977-82. PubMed ID: 2513733 [Abstract] [Full Text] [Related]
10. Effects of cyclo- and lipoxygenase inhibitors on hypoxic vasoconstriction in isolated ferret lungs. Gottlieb JE, McGeady M, Adkinson NF, Sylvester JT. J Appl Physiol (1985); 1988 Mar 26; 64(3):936-43. PubMed ID: 2835351 [Abstract] [Full Text] [Related]
12. Products of the lipoxygenase pathway in human natural killer cell cytotoxicity. Rossi P, Lindgren JA, Kullman C, Jondal M. Cell Immunol; 1985 Jun 26; 93(1):1-8. PubMed ID: 2986854 [Abstract] [Full Text] [Related]
13. Lipoxygenase pathway inhibition impairs the allograft response. Jordan ML, Carlson A, Hoffman RA, Simmons RL. Surgery; 1987 Aug 26; 102(2):248-55. PubMed ID: 3039676 [Abstract] [Full Text] [Related]
14. N-(4-chlorophenyl)-N-hydroxy-N'-(3-chlorophenyl)urea, a general reducing agent for 5-, 12-, and 15-lipoxygenases and a substrate for their pseudoperoxidase activities. Falgueyret JP, Desmarais S, Roy PJ, Riendeau D. Biochem Cell Biol; 1992 Aug 26; 70(3-4):228-36. PubMed ID: 1515123 [Abstract] [Full Text] [Related]