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Volumn 20, Issue 35, 2013, Pages 4386-4410

Medicinal chemistry of quinolines as emerging anti-inflammatory agents: An overview

Author keywords

Anti inflammatory drugs; COX; PDE4; Quinoline; Synthesis; TACE; TRPV1

Indexed keywords

AMIDE; ANTIINFLAMMATORY AGENT; CAPSAICIN; CARBOXYLIC ACID; CYCLOOXYGENASE 2 INHIBITOR; D 4418; GSK 256066; HYDROXAMIC ACID; IBUPROFEN; L 454560; N (3,5 DICHLORO 1 OXIDO 4 PYRIDINYL) 8 METHOXY 2 TRIFLUOROMETHYL 5 QUINOLINECARBOXAMIDE; NICOTINAMIDE; PHOSPHODIESTERASE IV INHIBITOR; PROSTAGLANDIN SYNTHASE; PROSTAGLANDIN SYNTHASE INHIBITOR; PYRIMIDINE DERIVATIVE; QUINOLINE DERIVATIVE; RESINIFERATOXIN; SCH 365351; THIAZINE DERIVATIVE; TUMOR NECROSIS FACTOR ALPHA CONVERTING ENZYME INHIBITOR; UNCLASSIFIED DRUG; VANILLOID RECEPTOR 1 ANTAGONIST;

EID: 84887917753     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/09298673113209990170     Document Type: Article
Times cited : (82)

References (96)
  • 1
    • 77954309291 scopus 로고    scopus 로고
    • Quinolines and structurally related heterocycles as antimalarials
    • Kaur, K.; Jain, M.; Reddy, R. P.; Jain, R. Quinolines and structurally related heterocycles as antimalarials. Eur. J. Med. Chem., 2010, 45(8), 3245-3264.
    • (2010) Eur. J. Med. Chem. , vol.45 , Issue.8 , pp. 3245-3264
    • Kaur, K.1    Jain, M.2    Reddy, R.P.3    Jain, R.4
  • 2
    • 0026680407 scopus 로고
    • Quinolone antimicrobial agents
    • Neu, H. C. Quinolone antimicrobial agents. Annu. Rev. Med., 1992, 43, 465-486.
    • (1992) Annu. Rev. Med. , vol.43 , pp. 465-486
    • Neu, H.C.1
  • 3
    • 24344486053 scopus 로고    scopus 로고
    • Synthesis of novel 4-substituted-7-trifluoromethylquinoline derivatives with nitric oxide releasing properties and their evaluation as analgesic and antiinflammatory agents
    • Abadi, A. H.; Hegazy, G. H.; El-Zaher, A. A. Synthesis of novel 4-substituted-7-trifluoromethylquinoline derivatives with nitric oxide releasing properties and their evaluation as analgesic and antiinflammatory agents. Bioorg. Med. Chem., 2005, 13(20), 5759-5765.
    • (2005) Bioorg. Med. Chem. , vol.13 , Issue.20 , pp. 5759-5765
    • Abadi, A.H.1    Hegazy, G.H.2    El-Zaher, A.A.3
  • 7
    • 79955004745 scopus 로고    scopus 로고
    • Quinoline as a privileged scaffold in cancer drug discovery
    • Solomon, V. R.; Lee, H. Quinoline as a privileged scaffold in cancer drug discovery. Curr. Med. Chem., 2011, 18(10), 1488-1508.
    • (2011) Curr. Med. Chem. , vol.18 , Issue.10 , pp. 1488-1508
    • Solomon, V.R.1    Lee, H.2
  • 8
    • 0034658440 scopus 로고    scopus 로고
    • Reversal of MRP-mediated doxorubicin resistance with quinoline-based drugs
    • Vezmar, M.; Georges, E. Reversal of MRP-Mediated Doxorubicin Resistance with Quinoline-Based Drugs. Biochem. Pharmacol., 2000, 59(10), 1245-1252.
    • (2000) Biochem. Pharmacol. , vol.59 , Issue.10 , pp. 1245-1252
    • Vezmar, M.1    Georges, E.2
  • 10
    • 0036566639 scopus 로고    scopus 로고
    • Atherosclerosis: The new view
    • Libby, P. Atherosclerosis: the new view. Sci. Am., 2002, 286(5), 46-55.
    • (2002) Sci. Am. , vol.286 , Issue.5 , pp. 46-55
    • Libby, P.1
  • 11
    • 33745571976 scopus 로고    scopus 로고
    • The immune response in atherosclerosis: A double-edged sword
    • Hansson, G. K.; Libby, P. The immune response in atherosclerosis: a double-edged sword. Nat. Rev. Immunol., 2006, 6(7), 508-519.
    • (2006) Nat. Rev. Immunol. , vol.6 , Issue.7 , pp. 508-519
    • Hansson, G.K.1    Libby, P.2
  • 12
    • 0031601339 scopus 로고    scopus 로고
    • The multienzyme PDE4 cyclic adenosine monophosphate-specific phosphodiesterase family: Intracellular targeting, regulation, and selective inhibition by compounds exerting anti-inflammatory and antidepressant actions
    • Houslay, M. D.; Sullivan, M.; Bolger, G. B. The multienzyme PDE4 cyclic adenosine monophosphate-specific phosphodiesterase family: intracellular targeting, regulation, and selective inhibition by compounds exerting anti-inflammatory and antidepressant actions. Adv. Pharmacol., 1998, 44, 225-342.
    • (1998) Adv. Pharmacol. , vol.44 , pp. 225-342
    • Houslay, M.D.1    Sullivan, M.2    Bolger, G.B.3
  • 13
    • 21144437565 scopus 로고    scopus 로고
    • Phosphodiesterase: Overview of protein structures, potential therapeutic applications and recent progress in drug development
    • Jeon, Y. H.; Heo, Y.-S.; Kim, C. M.; Hyun, Y.-L.; Lee, T. G.; Ro, S.; Cho, J. M. Phosphodiesterase: overview of protein structures, potential therapeutic applications and recent progress in drug development. Cell. Mol. Life Sci., 2005, 62(11), 1198-1220.
    • (2005) Cell. Mol. Life Sci. , vol.62 , Issue.11 , pp. 1198-1220
    • Jeon, Y.H.1    Heo, Y.-S.2    Kim, C.M.3    Hyun, Y.-L.4    Lee, T.G.5    Ro, S.6    Cho, J.M.7
  • 14
    • 15144351114 scopus 로고
    • Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford, U.K
    • Potter, B. V. L. In: Comprehensive Medicinal Chemistry; Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford, U.K., 1990, pp. 102-128.
    • (1990) Comprehensive Medicinal Chemistry , pp. 102-128
    • Potter, B.V.L.1
  • 15
    • 52449115420 scopus 로고    scopus 로고
    • Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease
    • Kodimuthali, A.; Jabaris, S. S. L.; Pal, M. Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease. J. Med. Chem., 2008, 51(18), 5471-5489.
    • (2008) J. Med. Chem. , vol.51 , Issue.18 , pp. 5471-5489
    • Kodimuthali, A.1    Jabaris, S.S.L.2    Pal, M.3
  • 17
    • 0034687225 scopus 로고    scopus 로고
    • Hunting the emesis and efficacy targets of PDE4 inhibitors: Identification of the photoaffinity probe 8-(3-azidophenyl)-6-[(4-iodo-1H-1- imidazolyl)methyl] quinoline (APIIMQ)
    • Macdonald, D.; Perrier, H.; Liu, S.; Laliberté, F.; Rasori, R.; Robichaud, A.; Masson, P.; Huang, Z. Hunting the emesis and efficacy targets of PDE4 inhibitors: identification of the photoaffinity probe 8-(3-azidophenyl)-6- [(4-iodo-1H-1-imidazolyl)methyl] quinoline (APIIMQ). J. Med. Chem., 2000, 43(21), 3820-3823.
    • (2000) J. Med. Chem. , vol.43 , Issue.21 , pp. 3820-3823
    • Macdonald, D.1    Perrier, H.2    Liu, S.3    Laliberté, F.4    Rasori, R.5    Robichaud, A.6    Masson, P.7    Huang, Z.8
  • 21
    • 0036179542 scopus 로고    scopus 로고
    • The new phosphodiesterase 4 inhibitor roflumilast is efficacious in exercise-induced asthma and leads to suppression of LPS-stimulated TNF-alpha ex vivo
    • Timmer, W.; Leclerc, V.; Birraux, G.; Neuhauser, M.; Hatzelmann, A.; Bethke, T.; Wurst, W. The new phosphodiesterase 4 inhibitor roflumilast is efficacious in exercise-induced asthma and leads to suppression of LPS-stimulated TNF-alpha ex vivo. J. Clin. Pharmacol., 2002, 42(3), 297-303.
    • (2002) J. Clin. Pharmacol. , vol.42 , Issue.3 , pp. 297-303
    • Timmer, W.1    Leclerc, V.2    Birraux, G.3    Neuhauser, M.4    Hatzelmann, A.5    Bethke, T.6    Wurst, W.7
  • 35
    • 80054788578 scopus 로고    scopus 로고
    • Novel 1-alkynyl substituted 1,2-dihydroquinoline derivatives from nimesulide (and their 2-oxo analogues): A new strategy to identify inhibitors of PDE4B
    • Pal, S.; Durgadas, S.; Nallapati, S.; Mukkanti, K.; Kapavarapu, R.; Meda, C. L. T.; Parsa, K. V. L.; Pal, M. Novel 1-alkynyl substituted 1,2-dihydroquinoline derivatives from nimesulide (and their 2-oxo analogues): A new strategy to identify inhibitors of PDE4B. Bioorg. Med. Chem. Lett., 2011, 21(21), 6573-6576.
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , Issue.21 , pp. 6573-6576
    • Pal, S.1    Durgadas, S.2    Nallapati, S.3    Mukkanti, K.4    Kapavarapu, R.5    Meda, C.L.T.6    Parsa, K.V.L.7    Pal, M.8
  • 36
    • 77951490751 scopus 로고    scopus 로고
    • Ceric ammonium nitrate: An efficient catalyst for one-pot synthesis of 2,2,4-trimethyl-1,2-dihydroquinolines
    • Durgadas, S.; Chatare, V. K.; Mukkanti, K.; Pal, S. Ceric ammonium nitrate: An efficient catalyst for one-pot synthesis of 2,2,4-trimethyl-1,2- dihydroquinolines. Lett. Org. Chem. 2010, 7(4), 306-310.
    • (2010) Lett. Org. Chem. , vol.7 , Issue.4 , pp. 306-310
    • Durgadas, S.1    Chatare, V.K.2    Mukkanti, K.3    Pal, S.4
  • 37
    • 0034926291 scopus 로고    scopus 로고
    • The vanilloid receptor: A molecular gateway to the pain pathway
    • Caterina, M. J.; Julius, D. The vanilloid receptor: a molecular gateway to the pain pathway. Annu. Rev. Neurosci., 2001, 24, 487-517.
    • (2001) Annu. Rev. Neurosci. , vol.24 , pp. 487-517
    • Caterina, M.J.1    Julius, D.2
  • 38
    • 0034954583 scopus 로고    scopus 로고
    • VR1 protein expression increases in undamaged DRG neurons after partial nerve injury
    • Hudson, L. J.; Bevan, S.; Wotherspoon, G.; Gentry, C.; Fox, A.; Winter, J. VR1 protein expression increases in undamaged DRG neurons after partial nerve injury. Eur. J. Neurosci., 2001, 13(11), 2105-2114.
    • (2001) Eur. J. Neurosci. , vol.13 , Issue.11 , pp. 2105-2114
    • Hudson, L.J.1    Bevan, S.2    Wotherspoon, G.3    Gentry, C.4    Fox, A.5    Winter, J.6
  • 39
    • 0037179755 scopus 로고    scopus 로고
    • P38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia
    • Ji, R. R.; Samad, T. A.; Jin, S. X.; Schmoll, R.; Woolf, C. J. p38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia. Neuron, 2002, 36(1), 57-68.
    • (2002) Neuron , vol.36 , Issue.1 , pp. 57-68
    • Ji, R.R.1    Samad, T.A.2    Jin, S.X.3    Schmoll, R.4    Woolf, C.J.5
  • 42
    • 65549133355 scopus 로고    scopus 로고
    • Vanilloid receptor antagonists: Emerging class of novel anti-inflammatory agents for pain management
    • Pal, M.; Angaru, S.; Kodimuthali, A.; Dhingra, N. Vanilloid Receptor Antagonists: Emerging Class of Novel Anti-Inflammatory Agents for Pain Management. Curr. Pharm. Des., 2009, 15(9), 1008-1026.
    • (2009) Curr. Pharm. Des. , vol.15 , Issue.9 , pp. 1008-1026
    • Pal, M.1    Angaru, S.2    Kodimuthali, A.3    Dhingra, N.4
  • 49
    • 84859805419 scopus 로고    scopus 로고
    • Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists
    • Saku, O.; Ishida, H.; Atsumi, E.; Sugimoto, Y.; Kodaira, H.; Kato, Y.; Shirakura, S.; Nakasato, Y. Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists. J. Med. Chem., 2012, 55(7), 3436-3451.
    • (2012) J. Med. Chem. , vol.55 , Issue.7 , pp. 3436-3451
    • Saku, O.1    Ishida, H.2    Atsumi, E.3    Sugimoto, Y.4    Kodaira, H.5    Kato, Y.6    Shirakura, S.7    Nakasato, Y.8
  • 50
    • 0028244816 scopus 로고
    • Tumor necrosis factor: A pleiotropic cytokine and therapeutic target
    • Tracey, K. J.; Cerami, A. Tumor necrosis factor: a pleiotropic cytokine and therapeutic target. Annu. Rev. Med., 1994, 45, 491-503.
    • (1994) Annu. Rev. Med. , vol.45 , pp. 491-503
    • Tracey, K.J.1    Cerami, A.2
  • 51
    • 0025809325 scopus 로고
    • Human tumor necrosis factor gene regulation in phorbol ester stimulated T and B cell lines
    • Goldfeld, A. E.; Strominger, J. L.; Doyle, C. Human Tumor Necrosis Factor Gene Regulation in Phorbol Ester Stimulated T and B Cell Lines. J. Exp. Med., 1991, 174(1), 73-81.
    • (1991) J. Exp. Med. , vol.174 , Issue.1 , pp. 73-81
    • Goldfeld, A.E.1    Strominger, J.L.2    Doyle, C.3
  • 52
    • 0032815883 scopus 로고    scopus 로고
    • Adamalysins. A family of metzincins including TNF-alpha converting enzyme (TACE)
    • Killar, L.; White, J.; Black, R.; Peschon, J. Adamalysins. A family of metzincins including TNF-alpha converting enzyme (TACE). Ann. NY Acad. Sci. 1999, 878, 442-452.
    • (1999) Ann. NY Acad. Sci. , vol.878 , pp. 442-452
    • Killar, L.1    White, J.2    Black, R.3    Peschon, J.4
  • 53
    • 0024281428 scopus 로고
    • A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF
    • Kriegler, M.; Perez, C.; Defay, K.; Albert, I.; Lu, S. D. A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF. Cell, 1988, 53(1), 45-53.
    • (1988) Cell , vol.53 , Issue.1 , pp. 45-53
    • Kriegler, M.1    Perez, C.2    Defay, K.3    Albert, I.4    Lu, S.D.5
  • 57
    • 0033863530 scopus 로고    scopus 로고
    • Ongoing trials with matrix metalloproteinase inhibitors
    • Brown, P. D. Ongoing trials with matrix metalloproteinase inhibitors. Exp. Opin. Invest. Drugs, 2000, 9(9), 2167-2177.
    • (2000) Exp. Opin. Invest. Drugs , vol.9 , Issue.9 , pp. 2167-2177
    • Brown, P.D.1
  • 58
    • 0033946952 scopus 로고    scopus 로고
    • Metalloproteinase inhibitors: New opportunities for the treatment of rheumatoid arthritis and osteoarthritis
    • Shaw, T.; Nixon, J. S.; Bottomley, K. M. Metalloproteinase inhibitors: new opportunities for the treatment of rheumatoid arthritis and osteoarthritis. Exp. Opin. Invest. Drugs, 2000, 9(7), 1469-1478.
    • (2000) Exp. Opin. Invest. Drugs , vol.9 , Issue.7 , pp. 1469-1478
    • Shaw, T.1    Nixon, J.S.2    Bottomley, K.M.3
  • 59
    • 0035056510 scopus 로고    scopus 로고
    • The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders
    • Elliot, S.; Cawston, T. The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders. Drugs Aging, 2001, 18(2), 87-99.
    • (2001) Drugs Aging , vol.18 , Issue.2 , pp. 87-99
    • Elliot, S.1    Cawston, T.2
  • 62
    • 0035341741 scopus 로고    scopus 로고
    • TACE and other ADAM proteases as targets for drug discovery
    • Moss, M. L.; White, J. M.; Lambert, M. H.; Andrews, R. C. TACE and other ADAM proteases as targets for drug discovery. Drug Discov. Today, 2001, 6(8), 417-426.
    • (2001) Drug Discov. Today , vol.6 , Issue.8 , pp. 417-426
    • Moss, M.L.1    White, J.M.2    Lambert, M.H.3    Andrews, R.C.4
  • 64
    • 19944376150 scopus 로고    scopus 로고
    • Non-hydroxamate 5-phenylpyrimidine-2,4,6-trione derivatives as selective inhibitors of tumor necrosis factor-converting enzyme
    • Duan, J. J.-W.; Lu, Z.; Wasserman, Z. R.; Liu, R.-Q.; Covington, M. B.; Decicco, C. P. Non-hydroxamate 5-phenylpyrimidine-2,4,6-trione derivatives as selective inhibitors of tumor necrosis factor-converting enzyme. Bioorg. Med. Chem. Lett., 2005, 15(12), 2970-2973.
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , Issue.12 , pp. 2970-2973
    • Duan, J.J.-W.1    Lu, Z.2    Wasserman, Z.R.3    Liu, R.-Q.4    Covington, M.B.5    Decicco, C.P.6
  • 72
    • 0033791318 scopus 로고    scopus 로고
    • Cyclooxygenases: Structural, cellular, and molecular biology
    • Smith, W. L.; DeWitt, D. L.; Garavito, R. M. Cyclooxygenases: structural, cellular, and molecular biology. Annu. Rev. Biochem., 2000, 69, 145-182.
    • (2000) Annu. Rev. Biochem. , vol.69 , pp. 145-182
    • Smith, W.L.1    Dewitt, D.L.2    Garavito, R.M.3
  • 74
    • 34147119080 scopus 로고    scopus 로고
    • Structural and functional basis of cyclooxygenase inhibition
    • Blobaum, A. L.; Marnett, L. J. Structural and Functional Basis of Cyclooxygenase Inhibition. J. Med. Chem., 2007, 50(7), 1425-1441.
    • (2007) J. Med. Chem. , vol.50 , Issue.7 , pp. 1425-1441
    • Blobaum, A.L.1    Marnett, L.J.2
  • 75
    • 75149177657 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of new 2,3-diarylquinoline derivatives as selective cyclooxygenase-2 inhibitors
    • Ghodsi, R.; Zarghi, A.; Daraei, B.; Hedayati, M. Design, synthesis and biological evaluation of new 2,3-diarylquinoline derivatives as selective cyclooxygenase-2 inhibitors. Bioorg. Med. Chem., 2010, 18(3), 1029-1033.
    • (2010) Bioorg. Med. Chem. , vol.18 , Issue.3 , pp. 1029-1033
    • Ghodsi, R.1    Zarghi, A.2    Daraei, B.3    Hedayati, M.4
  • 76
    • 67650083504 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new 4-carboxyl quinoline derivatives as cyclooxygenase-2 inhibitors
    • Zarghi, A.; Ghodsi, R.; Azizi, E.; Daraie, B.; Hedayati, M.; Dadrass, O. G. Synthesis and biological evaluation of new 4-carboxyl quinoline derivatives as cyclooxygenase-2 inhibitors. Bioorg. Med. Chem., 2009, 17(14), 5312-5317.
    • (2009) Bioorg. Med. Chem. , vol.17 , Issue.14 , pp. 5312-5317
    • Zarghi, A.1    Ghodsi, R.2    Azizi, E.3    Daraie, B.4    Hedayati, M.5    Dadrass, O.G.6
  • 77
    • 20944441781 scopus 로고    scopus 로고
    • Prostaglandinmediated control of rat brain kynurenic acid synthesis-opposite actions by COX-1 and COX-2 isoforms
    • Schwieler, L.; Erhardt, S.; Erhardt, C.; Engberg, G. Prostaglandinmediated control of rat brain kynurenic acid synthesis-opposite actions by COX-1 and COX-2 isoforms. J. Neural Transm., 2005, 112(7), 863-872.
    • (2005) J. Neural Transm. , vol.112 , Issue.7 , pp. 863-872
    • Schwieler, L.1    Erhardt, S.2    Erhardt, C.3    Engberg, G.4
  • 78
    • 0034047074 scopus 로고    scopus 로고
    • Glutamate and kynurenate in the rat central nervous system following treatments with tail ischaemia or diclofenac
    • Edwards, S. R.; Mather, L. E.; Lin, Y.; Power, I.; Cousins, M. J. Glutamate and kynurenate in the rat central nervous system following treatments with tail ischaemia or diclofenac. J. Pharm. Pharmacol., 2000, 52(1), 59-66.
    • (2000) J. Pharm. Pharmacol. , vol.52 , Issue.1 , pp. 59-66
    • Edwards, S.R.1    Mather, L.E.2    Lin, Y.3    Power, I.4    Cousins, M.J.5
  • 80
    • 0347990509 scopus 로고    scopus 로고
    • 1,2-Diaryl-1-ethanone and pyrazolo[4,3-c]quinoline-4-one as novel selective cyclooxygenase-2 inhibitors
    • Baruah, B.; Dasu, K.; Vaitilingam, B.; Vanguri, A.; Casturi, S. R.; Yeleswarapu, K. R. 1,2-Diaryl-1-ethanone and pyrazolo[4,3-c]quinoline-4-one as novel selective cyclooxygenase-2 inhibitors. Bioorg. Med. Chem. Lett., 2004, 14(2), 445-448.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , Issue.2 , pp. 445-448
    • Baruah, B.1    Dasu, K.2    Vaitilingam, B.3    Vanguri, A.4    Casturi, S.R.5    Yeleswarapu, K.R.6
  • 84
    • 0346059512 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory evaluation of 4-anilinofuro[2,3-b] quinoline and 4-phenoxyfuro[2,3-b]quinoline derivatives
    • Chen, Y.-L.; Chen, I.-L.; Lu, C.-M.; Tzeng, C.-C.; Tsao, L.-T.; Wang, J.-P. Synthesis and anti-inflammatory evaluation of 4-anilinofuro[2,3-b] quinoline and 4-phenoxyfuro[2,3-b]quinoline derivatives. Part 3. Bioorg. Med. Chem., 2004, 12(2), 387-392.
    • (2004) Part 3. Bioorg. Med. Chem. , vol.12 , Issue.2 , pp. 387-392
    • Chen, Y.-L.1    Chen, I.-L.2    Lu, C.-M.3    Tzeng, C.-C.4    Tsao, L.-T.5    Wang, J.-P.6
  • 85
    • 46449106774 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory activity evaluation of novel 7-alkoxy 1-amino-4,5-dihydro[1,2,4]triazole[4,3-A]quinolines
    • Sun, X.-Y.; Wei, C.-X.; Chai, K.-Y.; Piao, H.-R.; Quan, Z.-S. Synthesis and anti-inflammatory activity evaluation of novel 7-alkoxy 1-amino-4,5- dihydro[1,2,4]triazole[4,3-a]quinolines. Arch. Pharm. Chem. Life Sci., 2008, 341 (5), 288-293.
    • (2008) Arch. Pharm. Chem. Life Sci. , vol.341 , Issue.5 , pp. 288-293
    • Sun, X.-Y.1    Wei, C.-X.2    Chai, K.-Y.3    Piao, H.-R.4    Quan, Z.-S.5
  • 86
    • 1642409766 scopus 로고    scopus 로고
    • Tetrazolo[ 1,5-A]quinoline as a potential promising new scaffold for the synthesis of novel anti-inflammatory and antibacterial agents
    • Bekhit, A. A.; El-Sayed, O. A.; Aboulmagd, E.; Park, J. Y. Tetrazolo[ 1,5-a]quinoline as a potential promising new scaffold for the synthesis of novel anti-inflammatory and antibacterial agents. Eur. J. Med. Chem., 2004, 39(3), 249-255.
    • (2004) Eur. J. Med. Chem. , vol.39 , Issue.3 , pp. 249-255
    • Bekhit, A.A.1    El-Sayed, O.A.2    Aboulmagd, E.3    Park, J.Y.4
  • 87
    • 34447306306 scopus 로고    scopus 로고
    • Anti-inflammatory thiazine alkaloids isolated from the New Zealand Ascidian Aplidium sp. : IIInhibitors of the neutrophil respiratory burst in a model of gouty arthritis
    • Pearce, A. N.; Chia, E. W.; Berridge, M. V.; Clark, G. R.; Harper, J. L.; Larsen, L.; Maas, E. W.; Page, M. J.; Perry, N. B.; Webb, V. L.; Copp, B. R. Anti-inflammatory thiazine alkaloids isolated from the New Zealand Ascidian Aplidium sp.: Inhibitors of the neutrophil respiratory burst in a model of gouty arthritis. J. Nat. Prod., 2007, 70(6), 936-940.
    • (2007) J. Nat. Prod. , vol.70 , Issue.6 , pp. 936-940
    • Pearce, A.N.1    Chia, E.W.2    Berridge, M.V.3    Clark, G.R.4    Harper, J.L.5    Larsen, L.6    Maas, E.W.7    Page, M.J.8    Perry, N.B.9    Webb, V.L.10    Copp, B.R.11
  • 89
    • 40949138241 scopus 로고    scopus 로고
    • Synthesis, analgesic, anti-inflammatory, and antimicrobial activity of some novel pyrimido[4,5-b]quinolin-4-ones
    • El-Gazzar, A.-R. B. A.; El-Enanyb, M. M.; Mahmouda, M. N. Synthesis, analgesic, anti-inflammatory, and antimicrobial activity of some novel pyrimido[4,5-b]quinolin-4-ones. Bioorg. Med. Chem., 2008, 16(6), 3261-3273.
    • (2008) Bioorg. Med. Chem. , vol.16 , Issue.6 , pp. 3261-3273
    • El-Gazzar, A.-R.B.A.1    El-Enanyb, M.M.2    Mahmouda, M.N.3
  • 90
    • 61449168879 scopus 로고    scopus 로고
    • New acyclic nucleosides analogues as potential analgesic, antiinflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines Eur
    • El-Gazzar, A. B. A.; Hafez, H. N.; Nawwar, G. A. M. New acyclic nucleosides analogues as potential analgesic, antiinflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines Eur. J. Med. Chem., 2009, 44(4), 1427-1436.
    • (2009) J. Med. Chem. , vol.44 , Issue.4 , pp. 1427-1436
    • El-Gazzar, A.B.A.1    Hafez, H.N.2    Nawwar, G.A.M.3
  • 94
    • 84887877781 scopus 로고    scopus 로고
    • Available from: http://www.gsk-clinicalstudyregister.com/quicksearch- list.jsp?item=GSK256066&type=Compound&letterrange=G-K&studyType= All&phase=All&population=All&marketing=All.
  • 95
    • 84860662131 scopus 로고    scopus 로고
    • Anti-inflammatory iridoids of botanical origin
    • Viljoen, A.; Mncwangi, N.; Vermaak, I. Anti-Inflammatory Iridoids of Botanical Origin. Curr. Med. Chem., 2012, 19(14), 2104-2127.
    • (2012) Curr. Med. Chem. , vol.19 , Issue.14 , pp. 2104-2127
    • Viljoen, A.1    Mncwangi, N.2    Vermaak, I.3
  • 96
    • 84861881610 scopus 로고    scopus 로고
    • Discovery of selective small molecular TACE inhibitors for the treatment of rheumatoid arthritis
    • Li, N.G.; Shi, Z.H.; Tang, Y.P.; Wei-Li.; Lian-Yin.; Duan, J.A. Discovery of Selective Small Molecular TACE Inhibitors for the Treatment of Rheumatoid Arthritis. Curr. Med. Chem., 2012, 19(18), 2924-2956.
    • (2012) Curr. Med. Chem. , vol.19 , Issue.18 , pp. 2924-2956
    • Li, N.G.1    Shi, Z.H.2    Tang, Y.P.3


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