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114 related items for PubMed ID: 9167446
1. Lipoxygenase inhibitors, Part 6. Synthesis of new tetrahydropyrazine and other heterocyclic compounds by reaction of hydrazonoyl chlorides. Frohberg P, Wiese M, Nuhn P. Arch Pharm (Weinheim); 1997 Mar; 330(3):47-52. PubMed ID: 9167446 [Abstract] [Full Text] [Related]
2. Synthesis of 1,5-diarylpyrazol-3-propanoic acids towards inhibition of cyclooxygenase-1/2 activity and 5-lipoxygenase-mediated LTB4 formation. Ergün BC, Nuñez MT, Labeaga L, Ledo F, Darlington J, Bain G, Cakir B, Banoglu E. Arzneimittelforschung; 2010 Mar; 60(8):497-505. PubMed ID: 20863006 [Abstract] [Full Text] [Related]
3. Ca2+ ionophore A23187-stimulated secretion of azurophil granules in human polymorphonuclear leukocytes is largely mediated by endogenously formed leukotriene B4. Hatzelmann A, Fruchtmann R, Mohrs KH, Raddatz S, Müller-Peddinghaus R. Biochem Pharmacol; 1994 Jul 05; 48(1):31-9. PubMed ID: 8043028 [Abstract] [Full Text] [Related]
4. 4-acylaminophenol derivatives as novel lipoxygenase inhibitors: synthesis and inhibitory effect on 5-lipoxygenase and leukotriene B4 production. Kikuchi M, Hashimura Y, Tsuzurahara K, Nagasawa M, Inoue H, Taniguchi T, Uchida T. Biol Pharm Bull; 1994 Aug 05; 17(8):1038-46. PubMed ID: 7820104 [Abstract] [Full Text] [Related]
6. Mode of action of the new selective leukotriene synthesis inhibitor BAY X 1005 ((R)-2-[4-(quinolin-2-yl-methoxy)phenyl]-2-cyclopentyl acetic acid) and structurally related compounds. Hatzelmann A, Fruchtmann R, Mohrs KH, Raddatz S, Müller-Peddinghaus R. Biochem Pharmacol; 1993 Jan 07; 45(1):101-11. PubMed ID: 8381000 [Abstract] [Full Text] [Related]
7. Linoleic acid and dihomogammalinolenic acid inhibit leukotriene B4 formation and stimulate the formation of their 15-lipoxygenase products by human neutrophils in vitro. Evidence of formation of antiinflammatory compounds. Iversen L, Fogh K, Bojesen G, Kragballe K. Agents Actions; 1991 Jul 07; 33(3-4):286-91. PubMed ID: 1659156 [Abstract] [Full Text] [Related]
8. Naphthalenic lignan lactones as selective, nonredox 5-lipoxygenase inhibitors. Synthesis and biological activity of (methoxyalkyl)thiazole and methoxytetrahydropyran hybrids. Ducharme Y, Brideau C, Dubé D, Chan CC, Falgueyret JP, Gillard JW, Guay J, Hutchinson JH, McFarlane CS, Riendeau D. J Med Chem; 1994 Feb 18; 37(4):512-8. PubMed ID: 8120869 [Abstract] [Full Text] [Related]