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Volumn 9, Issue 5, 2009, Pages 452-463

Soluble epoxide hydrolase, a target with multiple opportunities for cardiovascular drug discovery

Author keywords

DHETs; Dihydroxyeicosatrienoic acids; EETs; Ephx2; Epoxyeicosatrienoic acids; P450 monooxygenase; Soluble epoxide hydrolase

Indexed keywords

12 (3 ADAMANTYL 1 YLUREIDO)DODECANOIC ACID; AEPO; BENZAMIDE DERIVATIVE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; ENZYME INHIBITOR; EPOXIDE HYDROLASE; EPOXYICOSATRIENOIC ACID; INTERCELLULAR ADHESION MOLECULE 1; N CYCLOHEXYL N DECYLUREA; PYRIDONE DERIVATIVE; SOLUBLE EPOXIDE HYDROLASE; SOLUBLE EPOXIDE HYDROLASE INHIBITOR; TUPS; UNCLASSIFIED DRUG; VASCULAR CELL ADHESION MOLECULE 1;

EID: 66649116553     PISSN: 15680266     EISSN: None     Source Type: Journal    
DOI: 10.2174/156802609788340805     Document Type: Review
Times cited : (44)

References (77)
  • 1
    • 34247867952 scopus 로고    scopus 로고
    • Cardiovascular therapeutic aspects of soluble epoxide hydrolase inhibitors
    • Imig, J. D. Cardiovascular therapeutic aspects of soluble epoxide hydrolase inhibitors. Cardio. Drug Rev. 2006, 24(2), 169-188.
    • (2006) Cardio. Drug Rev , vol.24 , Issue.2 , pp. 169-188
    • Imig, J.D.1
  • 2
    • 34548755151 scopus 로고    scopus 로고
    • The soluble epoxide hydrolase as a pharmaceutical target for hypertension
    • Chiamvimonvat, N.; Ho, C.-M.; Tsai, H.-J.; Hammock, B. D. The soluble epoxide hydrolase as a pharmaceutical target for hypertension. J. Cardiovasc. Pharmacol. 2007, 50(3), 225-237.
    • (2007) J. Cardiovasc. Pharmacol , vol.50 , Issue.3 , pp. 225-237
    • Chiamvimonvat, N.1    Ho, C.-M.2    Tsai, H.-J.3    Hammock, B.D.4
  • 3
    • 39749161642 scopus 로고    scopus 로고
    • Eicosanoids and renal damage in cardiometabolic syndrome
    • Imig, J. D. Eicosanoids and renal damage in cardiometabolic syndrome. Expert Opin. Drug Metab. Toxicol. 2008, 4(2), 165-174.
    • (2008) Expert Opin. Drug Metab. Toxicol , vol.4 , Issue.2 , pp. 165-174
    • Imig, J.D.1
  • 4
    • 13844316739 scopus 로고    scopus 로고
    • Epoxide hydrolases: Mechanisms, inhibitor designs, and biological roles
    • Morisseau, C.; Hammock, B. D. Epoxide hydrolases: Mechanisms, inhibitor designs, and biological roles. Annu. Rev. Pharmacol. Toxicol. 2005, 45, 311-333.
    • (2005) Annu. Rev. Pharmacol. Toxicol , vol.45 , pp. 311-333
    • Morisseau, C.1    Hammock, B.D.2
  • 5
    • 0037452577 scopus 로고    scopus 로고
    • The soluble epoxide hydrolase encoded by EPXH2 is a bifunctional enzyme with novel lipid phosphate phosphatase activity
    • Newman, J. W.; Morisseau, C.; Harris, T. R.; Hammock, B. D. The soluble epoxide hydrolase encoded by EPXH2 is a bifunctional enzyme with novel lipid phosphate phosphatase activity. Proc. Natl. Acad. Sci. USA 2003, 100, 1558-1563.
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , pp. 1558-1563
    • Newman, J.W.1    Morisseau, C.2    Harris, T.R.3    Hammock, B.D.4
  • 6
    • 1942438591 scopus 로고    scopus 로고
    • Structure of human epoxide hydrolase reveals mechanistic inferences on bifunctional catalysis in epoxide and phosphate ester hydrolysis
    • Gomez, G. A.; Morisseau, C.; Hammock, B. D.; Christianson, D. W. Structure of human epoxide hydrolase reveals mechanistic inferences on bifunctional catalysis in epoxide and phosphate ester hydrolysis. Biochemistry 2004, 43, 4716-4723.
    • (2004) Biochemistry , vol.43 , pp. 4716-4723
    • Gomez, G.A.1    Morisseau, C.2    Hammock, B.D.3    Christianson, D.W.4
  • 7
    • 0000353408 scopus 로고
    • The catalytic mechanism of microsomal epoxide hydrolase involves an ester intermediate
    • Lacourciere, G. M.; Armstrong, R. N. The catalytic mechanism of microsomal epoxide hydrolase involves an ester intermediate. J. Am. Chem. Soc. 1993, 115(22), 10466-10467.
    • (1993) J. Am. Chem. Soc , vol.115 , Issue.22 , pp. 10466-10467
    • Lacourciere, G.M.1    Armstrong, R.N.2
  • 9
    • 0034686018 scopus 로고    scopus 로고
    • Binding of alkylurea inhibitors to epoxide hydrolase implicates active site tyrosines in substrate activation
    • Argiriadi, M. A.; Morisseau, C.; Goodrow, M. H.; Dowdy, D. L.; Hammock, B. D.; Christianson, D. W. Binding of alkylurea inhibitors to epoxide hydrolase implicates active site tyrosines in substrate activation. J. Biol. Chem. 2000, 275(20), 15265-15270.
    • (2000) J. Biol. Chem , vol.275 , Issue.20 , pp. 15265-15270
    • Argiriadi, M.A.1    Morisseau, C.2    Goodrow, M.H.3    Dowdy, D.L.4    Hammock, B.D.5    Christianson, D.W.6
  • 10
    • 0034725581 scopus 로고    scopus 로고
    • Biochemical evidence for the involvement of tyrosine in epoxide activation during the catalytic cycle of epoxide hydrolase
    • Yamada, T.; Morisseau, C.; Maxwell, J. E.; Argiriadi, M. A.; Christianson, D. W.; Hammock, B. D. Biochemical evidence for the involvement of tyrosine in epoxide activation during the catalytic cycle of epoxide hydrolase. J. Biol. Chem. 2000, 275(30), 23082-23088.
    • (2000) J. Biol. Chem , vol.275 , Issue.30 , pp. 23082-23088
    • Yamada, T.1    Morisseau, C.2    Maxwell, J.E.3    Argiriadi, M.A.4    Christianson, D.W.5    Hammock, B.D.6
  • 11
    • 33749364917 scopus 로고    scopus 로고
    • Cytochrome P450 enzymes: Central players in cardiovascular health and disease
    • Elbekai, R. H.; El-Kadi, A. O. S. Cytochrome P450 enzymes: Central players in cardiovascular health and disease. Pharmacol. Ther. 2006, 112, 564-587.
    • (2006) Pharmacol. Ther , vol.112 , pp. 564-587
    • Elbekai, R.H.1    El-Kadi, A.O.S.2
  • 12
    • 33947375240 scopus 로고    scopus 로고
    • Action of epoxyeicosatrienoic acids on cellular function
    • Spector, A. A.; Norris, A. W. Action of epoxyeicosatrienoic acids on cellular function. Am. J. Pysiol. Cell Physiol. 2007, 292, C996-C1012.
    • (2007) Am. J. Pysiol. Cell Physiol , vol.292
    • Spector, A.A.1    Norris, A.W.2
  • 13
    • 0028090109 scopus 로고
    • Display of the characteristics of endothelium-derived hyperpolarizing factor by a cytochrome P450-derived arachidonic acid metabolite in the coronary microcirculation
    • Bauersachs, J.; Hecker, M.; Busse, R. Display of the characteristics of endothelium-derived hyperpolarizing factor by a cytochrome P450-derived arachidonic acid metabolite in the coronary microcirculation. Br. J. Pharmacol. 1994, 113, 1548-1553.
    • (1994) Br. J. Pharmacol , vol.113 , pp. 1548-1553
    • Bauersachs, J.1    Hecker, M.2    Busse, R.3
  • 14
    • 0030051805 scopus 로고    scopus 로고
    • Identification of epoxyeicosatrienoic acids as endothelium-derived hyperpolarization factors
    • Campbell, W. B.; Gebremedhin, D.; Pratt, P. F.; Harder, D. R. Identification of epoxyeicosatrienoic acids as endothelium-derived hyperpolarization factors. Circ. Res. 1996, 78, 415-423.
    • (1996) Circ. Res , vol.78 , pp. 415-423
    • Campbell, W.B.1    Gebremedhin, D.2    Pratt, P.F.3    Harder, D.R.4
  • 16
  • 18
    • 33644849675 scopus 로고    scopus 로고
    • Epoxyeicosatrienoic and dihydroxyeicosatrienoic acids dilate human coronary arterioles via BK(Ca) channels: Implications for soluble epoxide hydrolase inhibition
    • Larsen, B. T.; Miura, H.; Hatoum, O. A.; Campbell, W. B.; Hammock, B. D.; Zeldin, D. C.; Falck, J. R.; Gutterman, D. D. Epoxyeicosatrienoic and dihydroxyeicosatrienoic acids dilate human coronary arterioles via BK(Ca) channels: Implications for soluble epoxide hydrolase inhibition. Am. J. Physiol. Heart Circ. Physiol. 2006, 290, H491-H499.
    • (2006) Am. J. Physiol. Heart Circ. Physiol , vol.290
    • Larsen, B.T.1    Miura, H.2    Hatoum, O.A.3    Campbell, W.B.4    Hammock, B.D.5    Zeldin, D.C.6    Falck, J.R.7    Gutterman, D.D.8
  • 19
    • 33645815886 scopus 로고    scopus 로고
    • Endothelium-derived epoxyeicosatrienoic acids and vascular function
    • Fleming, I.; Busse, R. Endothelium-derived epoxyeicosatrienoic acids and vascular function. Hypertension 2006, 47, 629-633
    • (2006) Hypertension , vol.47 , pp. 629-633
    • Fleming, I.1    Busse, R.2
  • 20
    • 33644654633 scopus 로고    scopus 로고
    • Imig J. D.; Zhao Xueying; Zaharis C. Z.; Olearczyk J.J.; Pollock D. M.; Newman J. W.; Kim I. H.; Watanabe T.; Hammock B. D. An orally active epoxide hydrolase inhibitor lowers blood pressure and provides renal protection in salt-sensitive hypertension. Hypertension 2005, 46(4), 975-81.
    • Imig J. D.; Zhao Xueying; Zaharis C. Z.; Olearczyk J.J.; Pollock D. M.; Newman J. W.; Kim I. H.; Watanabe T.; Hammock B. D. An orally active epoxide hydrolase inhibitor lowers blood pressure and provides renal protection in salt-sensitive hypertension. Hypertension 2005, 46(4), 975-81.
  • 21
    • 34147160073 scopus 로고    scopus 로고
    • Loch, D.; H., Andrew; Morisseau, C.; Hammock, B. D.; Brown, L. Prevention of hypertension in DOCA-salt rats by an inhibitor of soluble epoxide hydrolase. Cell Biochem. Biophys. 2007, 47(1), 87-97.
    • Loch, D.; H., Andrew; Morisseau, C.; Hammock, B. D.; Brown, L. Prevention of hypertension in DOCA-salt rats by an inhibitor of soluble epoxide hydrolase. Cell Biochem. Biophys. 2007, 47(1), 87-97.
  • 22
    • 42149190687 scopus 로고    scopus 로고
    • Oral delivery of 1,3-dicyclohexylurea nanosus-pension enhances exposure and lowers blood pressure in hypertensive rats
    • Ghosh, S.; Chiang P.; Wahlstrom J. L.; Fujiwara H.; Selbo, J. G.; Roberds, S. L. Oral delivery of 1,3-dicyclohexylurea nanosus-pension enhances exposure and lowers blood pressure in hypertensive rats. Basic Clin. Pharmacol. Toxicol. 2008, 102(5), 453-458.
    • (2008) Basic Clin. Pharmacol. Toxicol , vol.102 , Issue.5 , pp. 453-458
    • Ghosh, S.1    Chiang, P.2    Wahlstrom, J.L.3    Fujiwara, H.4    Selbo, J.G.5    Roberds, S.L.6
  • 24
    • 0034704156 scopus 로고    scopus 로고
    • Targeted disruption of soluble epoxide hydrolase reveals a role in blood pressure regulation
    • Sinal, C. J.; Miyata, M.; Tohkin, M.; Nagata, K.; Bend, J. R.; Gonzalez. Targeted disruption of soluble epoxide hydrolase reveals a role in blood pressure regulation. J. Biol. Chem. 2000, 275(51), 40504-40510.
    • (2000) J. Biol. Chem , vol.275 , Issue.51 , pp. 40504-40510
    • Sinal, C.J.1    Miyata, M.2    Tohkin, M.3    Nagata, K.4    Bend, J.R.5    Gonzalez6
  • 28
    • 0033588034 scopus 로고    scopus 로고
    • Anti-inflammatory properties of cytochrome P450 epoxygenase-derived eicosanoids
    • Node, K.; Huo, Y.; Ruan, Z.-X.; Yang, B.; Spiecker, M.; Ley, K.; Zeldin, D. C.; Liao, J. K. Anti-inflammatory properties of cytochrome P450 epoxygenase-derived eicosanoids. Science 1999, 285(5431), 1276-1279.
    • (1999) Science , vol.285 , Issue.5431 , pp. 1276-1279
    • Node, K.1    Huo, Y.2    Ruan, Z.-X.3    Yang, B.4    Spiecker, M.5    Ley, K.6    Zeldin, D.C.7    Liao, J.K.8
  • 30
    • 33750529521 scopus 로고    scopus 로고
    • Inhibition of soluble epoxide hydrolase reduces LPS-induced thermal hyperalgesia and mechanical allodynia in a rat model of inflammatory pain
    • Inceoglu, B.; Jinks, S. L.; Schmelzer, K. R.; Waite, T.; Kim, I. H.; Hammock, B. D. Inhibition of soluble epoxide hydrolase reduces LPS-induced thermal hyperalgesia and mechanical allodynia in a rat model of inflammatory pain. Life Sci. 2006, 79(24), 2311-2319.
    • (2006) Life Sci , vol.79 , Issue.24 , pp. 2311-2319
    • Inceoglu, B.1    Jinks, S.L.2    Schmelzer, K.R.3    Waite, T.4    Kim, I.H.5    Hammock, B.D.6
  • 32
    • 66649091624 scopus 로고    scopus 로고
    • Webb, H.; Kay, H. Soluble epoxide hydrolase inhibitors for the treatment of rheumatoid arthritis and other autoimmune induced inflammation disorders. WO08058033A2, 2008.
    • Webb, H.; Kay, H. Soluble epoxide hydrolase inhibitors for the treatment of rheumatoid arthritis and other autoimmune induced inflammation disorders. WO08058033A2, 2008.
  • 33
    • 33845944050 scopus 로고    scopus 로고
    • Beyond vasodilation: Non-vasomotor roles of epoxyeicosatrienoic acids in the cardiovascular system
    • Larsen, B. T.; Campbell, W. B.; Gutterman, D. D. Beyond vasodilation: non-vasomotor roles of epoxyeicosatrienoic acids in the cardiovascular system. TRENDS Pharmacol. Sci. 2008, 28(1), 32-38.
    • (2008) TRENDS Pharmacol. Sci , vol.28 , Issue.1 , pp. 32-38
    • Larsen, B.T.1    Campbell, W.B.2    Gutterman, D.D.3
  • 36
    • 34548050872 scopus 로고    scopus 로고
    • Increasing or stabilizing renal epoxyeicosatrienoic acid production attenuates abnormal renal function and hypertension in obese rats
    • Huang, H.; Morisseau, C.; Wang, J. F.; Yang, T.; Falck, J. R.; Hammock, B. D.; Wang, M.-H. Increasing or stabilizing renal epoxyeicosatrienoic acid production attenuates abnormal renal function and hypertension in obese rats. Am. J. Physiol. 2007, 293(1), F342-F349.
    • (2007) Am. J. Physiol , vol.293 , Issue.1
    • Huang, H.1    Morisseau, C.2    Wang, J.F.3    Yang, T.4    Falck, J.R.5    Hammock, B.D.6    Wang, M.-H.7
  • 41
    • 1642458135 scopus 로고    scopus 로고
    • Polymorphism of the Soluble Epoxide Hydrolase is Associated with Coronary Artery Calicification in African-American Subjects - The Coronary Artery Risk Development in Young Adults (CARDIA) Study
    • Fornage, M.; Boerwinkle, E.; Doris, P. A.; Jacobs, D.; Liu, K.; Wong, N. D. Polymorphism of the Soluble Epoxide Hydrolase is Associated with Coronary Artery Calicification in African-American Subjects - The Coronary Artery Risk Development in Young Adults (CARDIA) Study. Circulation 2004, 109, 335-339.
    • (2004) Circulation , vol.109 , pp. 335-339
    • Fornage, M.1    Boerwinkle, E.2    Doris, P.A.3    Jacobs, D.4    Liu, K.5    Wong, N.D.6
  • 42
    • 33745222033 scopus 로고    scopus 로고
    • Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study
    • Lee, C. R.; North, K. E.; Bray, M. S.; Fornage, M.; Seubert, J. M.; Newman, J. W.; Hammock, B. D.; Couper, D. J.; Heiss, G.; Zeldin, D. C. Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study. Hum. Mol. Genet. 2006, 15(10), 1640-1649.
    • (2006) Hum. Mol. Genet , vol.15 , Issue.10 , pp. 1640-1649
    • Lee, C.R.1    North, K.E.2    Bray, M.S.3    Fornage, M.4    Seubert, J.M.5    Newman, J.W.6    Hammock, B.D.7    Couper, D.J.8    Heiss, G.9    Zeldin, D.C.10
  • 43
    • 10744225519 scopus 로고    scopus 로고
    • Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: Intrafamilial association study in an eight-generation hyperlipidemic kindred
    • Sato, K.; Emi, M.; Ezura, Y.; Fujita, Y.; Takada, D.; Ishigami, T.; Umemura, S.; Xin, Y.; Wu, L. L.; Larrinaga-Shum, S.; Stephenson, S. H.; Hunt, S. C., Hopkins, P. N. Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: Intrafamilial association study in an eight-generation hyperlipidemic kindred. J. Hum. Genet. 2004, 49, 29-34.
    • (2004) J. Hum. Genet , vol.49 , pp. 29-34
    • Sato, K.1    Emi, M.2    Ezura, Y.3    Fujita, Y.4    Takada, D.5    Ishigami, T.6    Umemura, S.7    Xin, Y.8    Wu, L.L.9    Larrinaga-Shum, S.10    Stephenson, S.H.11    Hunt, S.C.12    Hopkins, P.N.13
  • 44
    • 66649105010 scopus 로고    scopus 로고
    • Novel role of soluble epoxide hydrolase in regulating cholesterol in mammalian cells
    • Enayetallah, A.; Cao, L.; Grant, D. F. Novel role of soluble epoxide hydrolase in regulating cholesterol in mammalian cells. Open Drug Metabol. J. 2007, 1, 1-6.
    • (2007) Open Drug Metabol. J , vol.1 , pp. 1-6
    • Enayetallah, A.1    Cao, L.2    Grant, D.F.3
  • 46
    • 34250731775 scopus 로고    scopus 로고
    • Cytochrome P450 eicosanoids are activators of peroxisome proliferator-activated receptor α
    • Ng, V. Y.; Huang, Y.; Reddy, L. M.; Falck, J. R.; Lin, E. T.; Kroetz, D. L. Cytochrome P450 eicosanoids are activators of peroxisome proliferator-activated receptor α. Drug Metab. Dispos. 2007, 35(7), 1126-1134.
    • (2007) Drug Metab. Dispos , vol.35 , Issue.7 , pp. 1126-1134
    • Ng, V.Y.1    Huang, Y.2    Reddy, L.M.3    Falck, J.R.4    Lin, E.T.5    Kroetz, D.L.6
  • 47
  • 48
    • 66649084737 scopus 로고    scopus 로고
    • Webb, H.; Kay, H. Ureas as soluble epoxide hydrolase inhibitors for treatment of metabolic syndrome and related disorders and their preparation. WO08094869A1, 2008.
    • Webb, H.; Kay, H. Ureas as soluble epoxide hydrolase inhibitors for treatment of metabolic syndrome and related disorders and their preparation. WO08094869A1, 2008.
  • 49
    • 0020406326 scopus 로고
    • Chalcone oxides - potent selective inhibitors of cytosolic epoxide hydrolase
    • Mullin, C. A.; Hammock, B. D.; Chalcone oxides - potent selective inhibitors of cytosolic epoxide hydrolase. Arch. Biochem. Biophys. 1982, 216(2), 423-439.
    • (1982) Arch. Biochem. Biophys , vol.216 , Issue.2 , pp. 423-439
    • Mullin, C.A.1    Hammock, B.D.2
  • 50
    • 0032529615 scopus 로고    scopus 로고
    • Mechanism of mammalian soluble epoxide hydrolase inhibition by chalcone oxide derivatives
    • Morisseau, C.; Du, G.; Newman, J. W.; Hammock, B. D. Mechanism of mammalian soluble epoxide hydrolase inhibition by chalcone oxide derivatives. Arch. Biochem. Biophys. 1998, 356(2), 214-228.
    • (1998) Arch. Biochem. Biophys , vol.356 , Issue.2 , pp. 214-228
    • Morisseau, C.1    Du, G.2    Newman, J.W.3    Hammock, B.D.4
  • 54
    • 49249116223 scopus 로고    scopus 로고
    • Effects of the selective EET antagonist, 14,15-EEZE, on cardioprotection produced by exogenous or endogenous EETs in the canine heart
    • Gross, G. J.; Gauthier, K. M.; Moore, J.; Falck, J. R.; Hammock, B. D.; Campbell, W. B.; Nithipatikom, K. Effects of the selective EET antagonist, 14,15-EEZE, on cardioprotection produced by exogenous or endogenous EETs in the canine heart. Am. J. Physiol. 2008, 294(6), H2838-H2844.
    • (2008) Am. J. Physiol , vol.294 , Issue.6
    • Gross, G.J.1    Gauthier, K.M.2    Moore, J.3    Falck, J.R.4    Hammock, B.D.5    Campbell, W.B.6    Nithipatikom, K.7
  • 55
    • 33644697099 scopus 로고    scopus 로고
    • An epoxide hydrolase inhibitor, 12-(3- adamantyl-1-yl-ureido)dodecanoic acid (AUDA), reduces ischemic cerebral infarct size in stroke-prone spontaneously hypertensive rats
    • Dorrance, A. M.; Rupp, N.; Pollock, D. M.; Newman, J. W.; Hammock, D.; Imig, J. D. An epoxide hydrolase inhibitor, 12-(3- adamantyl-1-yl-ureido)dodecanoic acid (AUDA), reduces ischemic cerebral infarct size in stroke-prone spontaneously hypertensive rats. J. Cardio. Pharm. 2005, 46(6), 842-848.
    • (2005) J. Cardio. Pharm , vol.46 , Issue.6 , pp. 842-848
    • Dorrance, A.M.1    Rupp, N.2    Pollock, D.M.3    Newman, J.W.4    Hammock, D.5    Imig, J.D.6
  • 57
    • 33747331141 scopus 로고    scopus 로고
    • Synthesis and SAR of conformationally restricted inhibitors of soluble epoxide hydrolase
    • Jones, P. D.; Tsai, H.-J.; Do, Z. N.; Morisseau, C.; Hammock, B. D. Synthesis and SAR of conformationally restricted inhibitors of soluble epoxide hydrolase. Bioorg. Med. Chem. Lett. 2006, 16, 5212-5216.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , pp. 5212-5216
    • Jones, P.D.1    Tsai, H.-J.2    Do, Z.N.3    Morisseau, C.4    Hammock, B.D.5
  • 58
    • 35348826197 scopus 로고    scopus 로고
    • 1,3-disubstituted ureas functionalized with ether groups are potent inhibitors of the soluble epoxide hydrolase with improved pharmacokinetic properties
    • Kim, I.-H.; Tsai, H.-J.; Nishi, K.; Kasagami, T.; Morisseau, C.; Hammock, B. D. 1,3-disubstituted ureas functionalized with ether groups are potent inhibitors of the soluble epoxide hydrolase with improved pharmacokinetic properties. J. Med. Chem. 2007, 50(21), 5217-5226.
    • (2007) J. Med. Chem , vol.50 , Issue.21 , pp. 5217-5226
    • Kim, I.-H.1    Tsai, H.-J.2    Nishi, K.3    Kasagami, T.4    Morisseau, C.5    Hammock, B.D.6
  • 59
    • 34548070313 scopus 로고    scopus 로고
    • Orally bioavailable potent soluble epoxide hydrolase inhibitors
    • Hwang, S. H.; Tsai, H.-J.; Liu, J.-Y.; Morisseau, C.; Hammock, B. D. Orally bioavailable potent soluble epoxide hydrolase inhibitors. J. Med. Chem. 2007, 50, 3825-3840.
    • (2007) J. Med. Chem , vol.50 , pp. 3825-3840
    • Hwang, S.H.1    Tsai, H.-J.2    Liu, J.-Y.3    Morisseau, C.4    Hammock, B.D.5
  • 60
    • 66649136270 scopus 로고    scopus 로고
    • Gless, R. D., Jr. Preparation of phenyl urea and thiourea derivatives as soluble epoxide hydrolase inhibitors. WO08016884A2, 2008.
    • Gless, R. D., Jr. Preparation of phenyl urea and thiourea derivatives as soluble epoxide hydrolase inhibitors. WO08016884A2, 2008.
  • 61
    • 66649087842 scopus 로고    scopus 로고
    • Gless, R. D., Jr. Preparation of benzenesulfonamides as soluble epoxide hydrolase inhibitors for treating cardiovascular, inflammatory, pulmonary, and diabetes-related diseases. WO08040000A2, 2008.
    • Gless, R. D., Jr. Preparation of benzenesulfonamides as soluble epoxide hydrolase inhibitors for treating cardiovascular, inflammatory, pulmonary, and diabetes-related diseases. WO08040000A2, 2008.
  • 62
    • 66649113793 scopus 로고    scopus 로고
    • Gless, R. D., Jr.; Anandan, S. K.; Aavula, B. R. Phenylurea derivatives as soluble epoxide hydrolase inhibitors. WO08051873A2, 2008.
    • Gless, R. D., Jr.; Anandan, S. K.; Aavula, B. R. Phenylurea derivatives as soluble epoxide hydrolase inhibitors. WO08051873A2, 2008.
  • 63
    • 66649111728 scopus 로고    scopus 로고
    • Gless, R. D., Jr.; Anandan, S. K. Preparation of (piperidinyl)adamantanylurea derivatives for use as soluble epoxide hydrolase inhibitors. WO08051875A1, 2008.
    • Gless, R. D., Jr.; Anandan, S. K. Preparation of (piperidinyl)adamantanylurea derivatives for use as soluble epoxide hydrolase inhibitors. WO08051875A1, 2008.
  • 64
    • 66649101984 scopus 로고    scopus 로고
    • Hammock, B. D.; Jones, P. D.; Morriseau, C.; Huang, H.; Tsai, H.-J.; Gless, R. D., Jr. Piperidinyl, indolyl, piridinyl, morpholinyl, and benzimidazolyl urea derivatives as inhibitors of soluble epoxide hydrolase for the treatment of hypertension, inflammations and other diseases. WO2007106525A1.
    • Hammock, B. D.; Jones, P. D.; Morriseau, C.; Huang, H.; Tsai, H.-J.; Gless, R. D., Jr. Piperidinyl, indolyl, piridinyl, morpholinyl, and benzimidazolyl urea derivatives as inhibitors of soluble epoxide hydrolase for the treatment of hypertension, inflammations and other diseases. WO2007106525A1.
  • 65
    • 66649133935 scopus 로고    scopus 로고
    • Ingraham, R. H. Cyclic urea compounds as soluble epoxide hydrolase inhibitors effective for the treatment of cardiovascular disorders. WO07106706A1, 2007.
    • Ingraham, R. H. Cyclic urea compounds as soluble epoxide hydrolase inhibitors effective for the treatment of cardiovascular disorders. WO07106706A1, 2007.
  • 66
    • 66649105605 scopus 로고    scopus 로고
    • Delombaert, S.; Eldrup, A. B.; Kowalski, J. A.; Mugge, I. A.; Soleymanzadeh, F.; Swinamer, A. D.; Taylor, S. J. Preparation of piperidinecarboxylic acid benzylamides as soluble epoxide hydrolase inhibitors. WO07106705A1, 2007.
    • Delombaert, S.; Eldrup, A. B.; Kowalski, J. A.; Mugge, I. A.; Soleymanzadeh, F.; Swinamer, A. D.; Taylor, S. J. Preparation of piperidinecarboxylic acid benzylamides as soluble epoxide hydrolase inhibitors. WO07106705A1, 2007.
  • 67
    • 66649119866 scopus 로고    scopus 로고
    • Ingraham, R. H.; Proudfoot, J. R. Preparation of arylpyrazoles as soluble epoxide hydrolase inhibitors for the treatment of cardiovascular disease. WO03002555A1, 2003.
    • Ingraham, R. H.; Proudfoot, J. R. Preparation of arylpyrazoles as soluble epoxide hydrolase inhibitors for the treatment of cardiovascular disease. WO03002555A1, 2003.
  • 68
    • 66649086654 scopus 로고    scopus 로고
    • Fleck, R. W.; Guo, X.; Lo, H. Y.; Man, C. C. Substituted pyrazole compounds useful as soluble epoxide hydrolase inhibitors and their preparation and pharmaceutical compositions. WO07067836A2, 2007.
    • Fleck, R. W.; Guo, X.; Lo, H. Y.; Man, C. C. Substituted pyrazole compounds useful as soluble epoxide hydrolase inhibitors and their preparation and pharmaceutical compositions. WO07067836A2, 2007.
  • 69
    • 66649127072 scopus 로고    scopus 로고
    • Cywin, C. L.; De Lombaert, S.; Eldrup, A. B.; Ingraham, R. H.; Taylor, S.; Soleymanzadeh, F. Methods of using inhibitors of soluble epoxide hydrolase against hypertension and other disorders. WO06121719A2, 2006.
    • Cywin, C. L.; De Lombaert, S.; Eldrup, A. B.; Ingraham, R. H.; Taylor, S.; Soleymanzadeh, F. Methods of using inhibitors of soluble epoxide hydrolase against hypertension and other disorders. WO06121719A2, 2006.
  • 71
    • 66649121217 scopus 로고    scopus 로고
    • Eldrup, A. B.; Soleymanzadeh, F.; Taylor, S. J. N-substituted pyridones or pyrimidones, processes for preparing them, pharmaceutical compositions containing them, and their use as soluble epoxide hydrolase (sEH) inhibitors. WO07044491A1, 2007.
    • Eldrup, A. B.; Soleymanzadeh, F.; Taylor, S. J. N-substituted pyridones or pyrimidones, processes for preparing them, pharmaceutical compositions containing them, and their use as soluble epoxide hydrolase (sEH) inhibitors. WO07044491A1, 2007.
  • 72
    • 66649124742 scopus 로고    scopus 로고
    • Eldrup, A. B.; Farrow, N. A.; Kowalski, J. A.; Delombaert, S.; Mugge, I. A.; Soleymanzadeh, F.; Swinamer, A. D.; Taylor, S. J. Substituted pyridinamide compounds useful as soluble epoxide hydrolase inhibitors. WO07098352A2, 2007.
    • Eldrup, A. B.; Farrow, N. A.; Kowalski, J. A.; Delombaert, S.; Mugge, I. A.; Soleymanzadeh, F.; Swinamer, A. D.; Taylor, S. J. Substituted pyridinamide compounds useful as soluble epoxide hydrolase inhibitors. WO07098352A2, 2007.
  • 73
    • 66649101685 scopus 로고    scopus 로고
    • Ota, T.; Takahashi, H.; Kakinuma, H.; Busujima, T. Benzimidazole-5-carboxamide derivatives as soluble epoxide hydrolase inhibitors. WO07043653A1, 2007.
    • Ota, T.; Takahashi, H.; Kakinuma, H.; Busujima, T. Benzimidazole-5-carboxamide derivatives as soluble epoxide hydrolase inhibitors. WO07043653A1, 2007.
  • 74
    • 66649086376 scopus 로고    scopus 로고
    • Ota, T.; Hirano, H.; Kakinuma, H.; Shimaoka, T.; Kanno, H. Anilide compounds as soluble epoxide hydrolase inhibitors and pharmaceuticals containing them. JP2007126454A, 2007.
    • Ota, T.; Hirano, H.; Kakinuma, H.; Shimaoka, T.; Kanno, H. Anilide compounds as soluble epoxide hydrolase inhibitors and pharmaceuticals containing them. JP2007126454A, 2007.
  • 76
    • 66649103155 scopus 로고    scopus 로고
    • Ding, Y.; Marino, J. P.; Li, P.; Londregan, A. T. Novel soluble epoxide hydrolase inhibitors and their use. WO08105968A1, 2008.
    • Ding, Y.; Marino, J. P.; Li, P.; Londregan, A. T. Novel soluble epoxide hydrolase inhibitors and their use. WO08105968A1, 2008.
  • 77
    • 66649114070 scopus 로고    scopus 로고
    • Patel, D. V.; Gless, R. D., Jr.; Webb, H.; Kay, H.; Anandan, S. K.; Aavula, B. R. Preparation of α-hydroxyamide derivatives and analogs as soluble epoxide hydrolase inhibitors. WO08073623A2, 2008.
    • Patel, D. V.; Gless, R. D., Jr.; Webb, H.; Kay, H.; Anandan, S. K.; Aavula, B. R. Preparation of α-hydroxyamide derivatives and analogs as soluble epoxide hydrolase inhibitors. WO08073623A2, 2008.


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