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Journal Abstract Search

144 related items for PubMed ID: 1618754

  • 1. Identification of 5-oxo-15-hydroxy-6,8,11,13-eicosatetraenoic acid as a novel and potent human eosinophil chemotactic eicosanoid.
    Schwenk U, Morita E, Engel R, Schröder JM.
    J Biol Chem; 1992 Jun 25; 267(18):12482-8. PubMed ID: 1618754
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  • 4. The suppression of 5-lipoxygenation of arachidonic acid in human polymorphonuclear leucocytes by the 15-lipoxygenase product (15S)-hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoic acid: structure-activity relationship and mechanism of action.
    Petrich K, Ludwig P, Kühn H, Schewe T.
    Biochem J; 1996 Mar 15; 314 ( Pt 3)(Pt 3):911-6. PubMed ID: 8615788
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  • 5. 5-Oxo-eicosanoids are potent eosinophil chemotactic factors. Functional characterization and structural requirements.
    Schwenk U, Schröder JM.
    J Biol Chem; 1995 Jun 23; 270(25):15029-36. PubMed ID: 7797484
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  • 6. Inhibition of human natural killer cell activity by (14R,15S)-14,15-dihydroxy-5Z,8Z,10E,12E- icosatetraenoic acid.
    Ramstedt U, Serhan CN, Lundberg U, Wigzell H, Samuelsson B.
    Proc Natl Acad Sci U S A; 1984 Nov 23; 81(22):6914-8. PubMed ID: 6095260
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  • 7. Role of Human 15-Lipoxygenase-2 in the Biosynthesis of the Lipoxin Intermediate, 5S,15S-diHpETE, Implicated with the Altered Positional Specificity of Human 15-Lipoxygenase-1.
    Perry SC, Horn T, Tourdot BE, Yamaguchi A, Kalyanaraman C, Conrad WS, Akinkugbe O, Holinstat M, Jacobson MP, Holman TR.
    Biochemistry; 2020 Oct 27; 59(42):4118-4130. PubMed ID: 33048542
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  • 8. 5-Oxo-6,8,11,14-eicosatetraenoic acid is a potent stimulator of human eosinophil migration.
    Powell WS, Chung D, Gravel S.
    J Immunol; 1995 Apr 15; 154(8):4123-32. PubMed ID: 7706749
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  • 10. A novel dioxygenation product of arachidonic acid possesses potent chemotactic activity for human polymorphonuclear leukocytes.
    Shak S, Perez HD, Goldstein IM.
    J Biol Chem; 1983 Dec 25; 258(24):14948-53. PubMed ID: 6317681
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  • 11. Arachidonate 12-lipoxygenase purified from porcine leukocytes by immunoaffinity chromatography and its reactivity with hydroperoxyeicosatetraenoic acids.
    Yokoyama C, Shinjo F, Yoshimoto T, Yamamoto S, Oates JA, Brash AR.
    J Biol Chem; 1986 Dec 15; 261(35):16714-21. PubMed ID: 3782139
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  • 12. Drosophila Fed ARA and EPA Yields Eicosanoids, 15S-Hydroxy-5Z,8Z, 11Z, 13E-Eicosatetraenoic Acid, and 15S-Hydroxy-5Z,8Z,11Z,13E,17Z-Eicosapentaenoic Acid.
    Tan L, Xin X, Zhai L, Shen L.
    Lipids; 2016 Apr 15; 51(4):435-49. PubMed ID: 26931457
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  • 13. Hyperalgesic properties of 15-lipoxygenase products of arachidonic acid.
    Levine JD, Lam D, Taiwo YO, Donatoni P, Goetzl EJ.
    Proc Natl Acad Sci U S A; 1986 Jul 15; 83(14):5331-4. PubMed ID: 3014543
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  • 14. Synthesis and 5-lipoxygenase inhibitory activities of eicosanoid compounds.
    Arai Y, Shimoji K, Konno M, Konishi Y, Okuyama S, Iguchi S, Hayashi M, Miyamoto T, Toda M.
    J Med Chem; 1983 Jan 15; 26(1):72-8. PubMed ID: 6298421
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  • 15. Synthesis of 11,12-leukotriene A4, 11S,12S-oxido-5Z,7E,9E,14Z-eicosatetraenoic acid, a novel leukotriene of the 12-lipoxygenase pathway.
    Kitamura S, Shimizu T, Izumi T, Seyama Y.
    FEBS Lett; 1987 Mar 09; 213(1):169-73. PubMed ID: 3556576
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  • 16. A simple method for the preparation of (5Z,8Z,11Z,14Z)-16-hydroxyeicosa-5,8,11,14-tetraenoic acid enantiomers and the corresponding 14,15-dehydro analogues: role of the 16-hydroxy group for the lipoxygenase reaction.
    Ivanov IV, Romanov SG, Groza NV, Nigam S, Kuhn H, Myagkova GI.
    Bioorg Med Chem; 2002 Jul 09; 10(7):2335-43. PubMed ID: 11983531
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  • 18. Identification of novel arachidonic acid metabolites formed by prostaglandin H synthase.
    Hecker M, Ullrich V, Fischer C, Meese CO.
    Eur J Biochem; 1987 Nov 16; 169(1):113-23. PubMed ID: 3119336
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  • 19. Substrate selectivity of 5-hydroxyeicosanoid dehydrogenase and its inhibition by 5-hydroxy-Delta6-long-chain fatty acids.
    Patel P, Cossette C, Anumolu JR, Erlemann KR, Grant GE, Rokach J, Powell WS.
    J Pharmacol Exp Ther; 2009 Apr 16; 329(1):335-41. PubMed ID: 19164464
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