메뉴 건너뛰기




Volumn 40, Issue 13, 1997, Pages 1955-1968

Structure-activity relationships of N-hydroxyurea 5-lipoxygenase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

ARACHIDONATE 5 LIPOXYGENASE; HYDROXYUREA; LIPOXYGENASE INHIBITOR; N [3 [5 (4 FLUOROPHENOXY) 2 FURYL] 1 METHYL 2 PROPYNYL] N HYDROXYUREA; UNCLASSIFIED DRUG;

EID: 15144342082     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9700474     Document Type: Article
Times cited : (39)

References (43)
  • 1
    • 0028216249 scopus 로고
    • Moderating the inflammation of asthma: Inhibiting the production or action of products of the 5-lipoxygenase pathway
    • (a) Israel, E. Moderating the inflammation of asthma: inhibiting the production or action of products of the 5-lipoxygenase pathway. Ann. Allergy 1994, 72, 279-284.
    • (1994) Ann. Allergy , vol.72 , pp. 279-284
    • Israel, E.1
  • 2
    • 0028207993 scopus 로고
    • Progress with investigational drugs for the treatment of pulmonary and inflammatory diseases
    • (b) Brooks, D. W. Progress with investigational drugs for the treatment of pulmonary and inflammatory diseases. Expert Opin. Invest. Drugs 1994, 3, 185-190.
    • (1994) Expert Opin. Invest. Drugs , vol.3 , pp. 185-190
    • Brooks, D.W.1
  • 3
    • 0020597565 scopus 로고
    • Leukotrienes: Mediators of immediate hypersensitivity reactions and inflammation
    • Samuelsson, B. Leukotrienes: mediators of immediate hypersensitivity reactions and inflammation. Science 1983, 220, 568-575.
    • (1983) Science , vol.220 , pp. 568-575
    • Samuelsson, B.1
  • 5
    • 0019352080 scopus 로고
    • Leukotrienes: A major step in understanding immediate hypersensitivity reactions
    • (b) Borgeat, P.; Sirois, P. Leukotrienes: a major step in understanding immediate hypersensitivity reactions. J. Med. Chem. 1981, 24, 121-126.
    • (1981) J. Med. Chem. , vol.24 , pp. 121-126
    • Borgeat, P.1    Sirois, P.2
  • 6
    • 0029946682 scopus 로고    scopus 로고
    • Modulators of Lekotriene Biosynthesis and Receptor Activation
    • Brooks, C. D. W.; Summers, J. B. Modulators of Lekotriene Biosynthesis and Receptor Activation. J. Med. Chem. 1996, 39, 2629-2654.
    • (1996) J. Med. Chem. , vol.39 , pp. 2629-2654
    • Brooks, C.D.W.1    Summers, J.B.2
  • 7
    • 0025040476 scopus 로고
    • Leukocyte arachidonate 5-lipoxygenase isolation and characterization
    • (a) Rouzer, C. A.; Samuelsson, B. Leukocyte arachidonate 5-lipoxygenase isolation and characterization. Methods Enzymol. 1990, 187, 312-319.
    • (1990) Methods Enzymol. , vol.187 , pp. 312-319
    • Rouzer, C.A.1    Samuelsson, B.2
  • 8
    • 0027932967 scopus 로고
    • 5-Lipoxygenase: Enzyme expression and regulation of activity
    • (b) Steinhilber, D. 5-Lipoxygenase: enzyme expression and regulation of activity. Pharm. Acta Helv. 1994, 69, 3-14.
    • (1994) Pharm. Acta Helv. , vol.69 , pp. 3-14
    • Steinhilber, D.1
  • 10
    • 0025883217 scopus 로고
    • Human 5-lipoxygenase contains an essential iron
    • Percival, M. D. Human 5-lipoxygenase contains an essential iron. J. Biol. Chem. 1991, 266, 10058-10061.
    • (1991) J. Biol. Chem. , vol.266 , pp. 10058-10061
    • Percival, M.D.1
  • 11
    • 0026736070 scopus 로고
    • 5-Lipoxygenase: Properties, pharmacology and the quinolinyl(bridged)aryl class of inhibitors
    • (a) Musser, J. H.; Kreft, A. F. 5-Lipoxygenase: properties, pharmacology and the quinolinyl(bridged)aryl class of inhibitors. J. Med. Chem. 1992, 35, 2502-2524.
    • (1992) J. Med. Chem. , vol.35 , pp. 2502-2524
    • Musser, J.H.1    Kreft, A.F.2
  • 12
    • 0025808251 scopus 로고
    • Hydroxamic acids and hydroxyureas as inhibitors of arachidonate 5-lipoxygenase
    • (b) Garland, L. G.; Salmon, J. A. Hydroxamic acids and hydroxyureas as inhibitors of arachidonate 5-lipoxygenase. Drugs Future 1991, 16, 547-558.
    • (1991) Drugs Future , vol.16 , pp. 547-558
    • Garland, L.G.1    Salmon, J.A.2
  • 13
    • 0027014761 scopus 로고
    • 5-Lipoxygenase inhibitors and their anti-inflammatory activities
    • Ellis, G. P., Luscombe, D. K., Eds.; Elsevier Science Publishers: New York
    • (c) Batt, D. G. 5-Lipoxygenase inhibitors and their anti-inflammatory activities. In Progress in Medicinal Chemistry; Ellis, G. P., Luscombe, D. K., Eds.; Elsevier Science Publishers: New York, 1992; Vol. 29, pp 1-63.
    • (1992) Progress in Medicinal Chemistry , vol.29 , pp. 1-63
    • Batt, D.G.1
  • 14
    • 0026725367 scopus 로고
    • Designing therapeutically effective 5-lipoxygenase inhibitors
    • (d) McMillan, R. M.; Walker, E. R. H. Designing therapeutically effective 5-lipoxygenase inhibitors. Trends Pharmacol. Sci. 1992, 13, 323-330.
    • (1992) Trends Pharmacol. Sci. , vol.13 , pp. 323-330
    • McMillan, R.M.1    Walker, E.R.H.2
  • 15
    • 0021365007 scopus 로고
    • Rationally designed, potent competitive inhibitors of leukotriene biosynthesis
    • Corey, E. J.; Cashman, J. R.; Kanter, S. S.; Corey, D. R. Rationally designed, potent competitive inhibitors of leukotriene biosynthesis. J. Am. Chem. Soc. 1984, 106, 1503-1504.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1503-1504
    • Corey, E.J.1    Cashman, J.R.2    Kanter, S.S.3    Corey, D.R.4
  • 23
    • 0002491936 scopus 로고
    • The discovery of zileuton
    • Merluzzi, V. J., Adams, J., Eds.; Birkhauser: Boston, Chapter 5
    • Brooks, D. W.; Carter, G. W. The discovery of zileuton. In The Search for Anti-Inflammatory Drugs; Merluzzi, V. J., Adams, J., Eds.; Birkhauser: Boston, 1995; Chapter 5, pp 129-160.
    • (1995) The Search for Anti-Inflammatory Drugs , pp. 129-160
    • Brooks, D.W.1    Carter, G.W.2
  • 24
    • 0026332275 scopus 로고
    • Pharmacokinetics, safety and ability to diminish leukotriene synthesis by zileuton, an inhibitor of 5-lipoxygenase
    • Ackerman, N. R., Bonney, R. J., Welton, A. F., Eds.; Birkhauser: Basel
    • (a) Rubin, P.; Dubé, L.; Braeckman, R.; Swanson, L.; Hanson, R.; Albert, D.; Carter, G. Pharmacokinetics, safety and ability to diminish leukotriene synthesis by zileuton, an inhibitor of 5-lipoxygenase. In Progress in Inflammation, Research and Therapy; Ackerman, N. R., Bonney, R. J., Welton, A. F., Eds.; Birkhauser: Basel, 1991; pp 103-116.
    • (1991) Progress in Inflammation, Research and Therapy , pp. 103-116
    • Rubin, P.1    Dubé, L.2    Braeckman, R.3    Swanson, L.4    Hanson, R.5    Albert, D.6    Carter, G.7
  • 25
    • 0344274371 scopus 로고
    • Pharmacokinetics and metabolism of the new 5-lipoxygenase inhibitor A-64077 after single oral administration in man
    • (b) Braeckman, R. A.; Granneman, R.; Rubin, P. R.; Kesterson, J. W. Pharmacokinetics and metabolism of the new 5-lipoxygenase inhibitor A-64077 after single oral administration in man. J. Clin. Pharmacol. 1989, 29, 837.
    • (1989) J. Clin. Pharmacol. , vol.29 , pp. 837
    • Braeckman, R.A.1    Granneman, R.2    Rubin, P.R.3    Kesterson, J.W.4
  • 27
    • 0013295291 scopus 로고
    • Chemistry of Amine-Boranes. Part 5. Reduction of Oximes, O-Acyl-oximes, and O-Alkyl-oximes with Pyridine-Borane in Acid
    • Kawase, M.; Kikugawa, Y. Chemistry of Amine-Boranes. Part 5. Reduction of Oximes, O-Acyl-oximes, and O-Alkyl-oximes with Pyridine-Borane in Acid. J. Chem. Soc., Perkin 1 Trans. 1979, 643-645.
    • (1979) J. Chem. Soc., Perkin 1 Trans. , pp. 643-645
    • Kawase, M.1    Kikugawa, Y.2
  • 28
    • 4043071644 scopus 로고
    • The Cyanohydridoborate Anion as a Selective Reducing Agent
    • Borch, R. F.; Bernstien, M. D.; Dupont Durst, H. The Cyanohydridoborate Anion as a Selective Reducing Agent. J. Am. Chem. Soc. 1971, 93, 2897-2904.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 2897-2904
    • Borch, R.F.1    Bernstien, M.D.2    Dupont Durst, H.3
  • 30
    • 85064399949 scopus 로고
    • Boron Trifluoride Promoted Addition of Organolithiums to Oxime Ethers. A Facile Synthesis of Substituted Hydroxylamines
    • Uno, H.; Terakawa, T.; Suzuki, H. Boron Trifluoride Promoted Addition of Organolithiums to Oxime Ethers. A Facile Synthesis of Substituted Hydroxylamines. Synlett 1991, 559-560.
    • (1991) Synlett , pp. 559-560
    • Uno, H.1    Terakawa, T.2    Suzuki, H.3
  • 31
    • 0025784591 scopus 로고
    • Addition of Organolithium Compounds to N-THP Protected Nitrones
    • Basha, A.; Ratajczyk, J. D.; Brooks, D. W. Addition Of Organolithium Compounds To N-THP Protected Nitrones. Tetrahedron Lett. 1991, 32, 3783-3786.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 3783-3786
    • Basha, A.1    Ratajczyk, J.D.2    Brooks, D.W.3
  • 32
    • 0023023425 scopus 로고
    • An Improved Synthesis of N-hydroxyamino Acids and Thier Esters Using (Z)-2-Furaldehyde Oxime
    • Goto, G.; Kawakita, K.; Okutani, T.; Miki, T. An Improved Synthesis of N-hydroxyamino Acids and Thier Esters Using (Z)-2-Furaldehyde Oxime. Chem. Pharm. Bull. 1986, 34, 3202-3207.
    • (1986) Chem. Pharm. Bull. , vol.34 , pp. 3202-3207
    • Goto, G.1    Kawakita, K.2    Okutani, T.3    Miki, T.4
  • 33
    • 0020618817 scopus 로고
    • Natural Ferric Ionophores: Total Synthesis of Schizokinen, Schizokinen A, and Arthrobactin
    • Lee, B. H.; Miller, M. J. Natural Ferric Ionophores: Total Synthesis of Schizokinen, Schizokinen A, and Arthrobactin. J. Org. Chem. 1983, 48, 24-31.
    • (1983) J. Org. Chem. , vol.48 , pp. 24-31
    • Lee, B.H.1    Miller, M.J.2
  • 34
    • 0000529702 scopus 로고
    • N,O-Bis(phenoxycarbonyl)hydroxylamine: A new reagent for the direct synthesis of substituted N-hydroxyureas
    • Stewart, A. O.; Brooks, D. W. N,O-Bis(phenoxycarbonyl)hydroxylamine: a new reagent for the direct synthesis of substituted N-hydroxyureas. J. Org. Chem. 1992, 57, 5020-5023.
    • (1992) J. Org. Chem. , vol.57 , pp. 5020-5023
    • Stewart, A.O.1    Brooks, D.W.2
  • 39
    • 0023877313 scopus 로고
    • Acetohydroxamic Acids as Potent, Selective, Orally Active 5-Lipoxygenase Inhibitors
    • Jackson, W. P.; Islip, P. J.; Kneen, G.; Pugh, A.; Wates, P. J. Acetohydroxamic Acids as Potent, Selective, Orally Active 5-Lipoxygenase Inhibitors. J. Med. Chem. 1988, 31, 499-500.
    • (1988) J. Med. Chem. , vol.31 , pp. 499-500
    • Jackson, W.P.1    Islip, P.J.2    Kneen, G.3    Pugh, A.4    Wates, P.J.5
  • 43
    • 0000021639 scopus 로고
    • Chemistry of Thienopyridines. III. Syntheses of Thieno-[2,3-b]- and Thieno[3,2-b]pyridine Systems. Direct Substitution into the Former System
    • Klemm, L. H.; Klopfenstein, C. E.; Zell, R.; McCoy, D. R.; Klemm, R. A. Chemistry of Thienopyridines. III. Syntheses of Thieno-[2,3-b]- and Thieno[3,2-b]pyridine Systems. Direct Substitution into the Former System. J. Org. Chem. 1969, 34, 347-354.
    • (1969) J. Org. Chem. , vol.34 , pp. 347-354
    • Klemm, L.H.1    Klopfenstein, C.E.2    Zell, R.3    McCoy, D.R.4    Klemm, R.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.