메뉴 건너뛰기




Volumn 83, Issue 5, 2012, Pages 896-900

Anti-neuroinflammatory constituents from Polygala tricornis Gagnep

Author keywords

Methylene butyrolactam derivative; 5 hydroxymethyl furfural derivative; Anti neuroinflammation; Polygala tricornis

Indexed keywords

(5 FORMYLFURAN 2 YL)METHYL 4 HYDROXY 2 METHYLENEBUTANOATE; ANTIINFLAMMATORY AGENT; BUTYL 4 METHYLENE 5 OXO PYRROLIDIN 2 CARBOXYLATE; ESCHERICHIA COLI LIPOPOLYSACCHARIDE; NITRIC OXIDE; PLANT EXTRACT; POLYGALA TRICORNIS EXTRACT; UNCLASSIFIED DRUG;

EID: 84861595021     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2012.03.025     Document Type: Article
Times cited : (38)

References (30)
  • 1
    • 18844374851 scopus 로고    scopus 로고
    • Neuroinflammatory processes in Parkinson's disease
    • E.C. Hirsch, S. Hunot, and A. Hartmann Neuroinflammatory processes in Parkinson's disease Parkinsonism Relat Disord 11 Suppl. 1 2005 S9 S15
    • (2005) Parkinsonism Relat Disord , vol.11 , Issue.SUPPL. 1
    • Hirsch, E.C.1    Hunot, S.2    Hartmann, A.3
  • 3
    • 4944258716 scopus 로고    scopus 로고
    • The role of inflammation in Alzheimer's disease
    • E.E. Tuppo, and H.R. Arias The role of inflammation in Alzheimer's disease Int J Biochem Cell Biol 37 2005 289 305
    • (2005) Int J Biochem Cell Biol , vol.37 , pp. 289-305
    • Tuppo, E.E.1    Arias, H.R.2
  • 4
    • 33644516288 scopus 로고    scopus 로고
    • Contribution of inflammatory processes to Alzheimer's disease: Molecular mechanisms
    • M. Sastre, T. Klockgether, and M.T. Heneka Contribution of inflammatory processes to Alzheimer's disease: molecular mechanisms Int J Dev Neurosci 24 2006 167 176
    • (2006) Int J Dev Neurosci , vol.24 , pp. 167-176
    • Sastre, M.1    Klockgether, T.2    Heneka, M.T.3
  • 5
    • 0026628844 scopus 로고
    • Immune regulation by brain cells in the central nervous system: Microglia but not astrocytes present myelin basic protein to encephalitogenic T cells under in vivo-mimicking conditions
    • Y. Matsumoto, K. Ohmori, and M. Fujiwara Immune regulation by brain cells in the central nervous system: microglia but not astrocytes present myelin basic protein to encephalitogenic T cells under in vivo-mimicking conditions Immunology 76 1992 209 216
    • (1992) Immunology , vol.76 , pp. 209-216
    • Matsumoto, Y.1    Ohmori, K.2    Fujiwara, M.3
  • 6
    • 0037215645 scopus 로고    scopus 로고
    • Role of microglia in inflammation-mediated neurodegenerative diseases: Mechanisms and strategies for therapeutic intervention
    • B. Liu, and J.S. Hong Role of microglia in inflammation-mediated neurodegenerative diseases: mechanisms and strategies for therapeutic intervention J Pharmacol Exp Ther 304 2003 1 7
    • (2003) J Pharmacol Exp Ther , vol.304 , pp. 1-7
    • Liu, B.1    Hong, J.S.2
  • 7
    • 28444498107 scopus 로고    scopus 로고
    • Role of nitric oxide in Parkinson's disease
    • L. Zhang, V.L. Dawson, and T.M. Dawson Role of nitric oxide in Parkinson's disease Pharmacol Ther 109 2006 33 41
    • (2006) Pharmacol Ther , vol.109 , pp. 33-41
    • Zhang, L.1    Dawson, V.L.2    Dawson, T.M.3
  • 8
    • 33750465142 scopus 로고    scopus 로고
    • Nitric oxidesynthase regulation and diversity: Implications in Parkinson's disease
    • R. Kavya, R. Saluja, S. Singh, and M. Dikshit Nitric oxidesynthase regulation and diversity: implications in Parkinson's disease Nitric Oxide 15 2006 280 294
    • (2006) Nitric Oxide , vol.15 , pp. 280-294
    • Kavya, R.1    Saluja, R.2    Singh, S.3    Dikshit, M.4
  • 9
    • 56349089470 scopus 로고    scopus 로고
    • Role of nitric oxide synthases in Parkinson's disease: A review on the antioxidant and anti-inflammatory activity of polyphenols
    • K. Aquilano, S. Baldelli, G. Rotilio, and R. Ciriolo Role of nitric oxide synthases in Parkinson's disease: a review on the antioxidant and anti-inflammatory activity of polyphenols Neurochem Res 33 2008 2416 2426
    • (2008) Neurochem Res , vol.33 , pp. 2416-2426
    • Aquilano, K.1    Baldelli, S.2    Rotilio, G.3    Ciriolo, R.4
  • 10
    • 20444487788 scopus 로고    scopus 로고
    • Tricornoses A-L, oligosaccharide multi-esters from the roots of Polygala tricornis
    • J. Li, Y. Jiang, and P.F. Tu Tricornoses A-L, oligosaccharide multi-esters from the roots of Polygala tricornis J Nat Prod 68 2005 739 744
    • (2005) J Nat Prod , vol.68 , pp. 739-744
    • Li, J.1    Jiang, Y.2    Tu, P.F.3
  • 11
    • 30544440054 scopus 로고    scopus 로고
    • Xanthone O-glycosides and benzophenone O-glycosides from the roots of Polygala tricornis
    • J. Li, Y. Jiang, and P.F. Tu Xanthone O-glycosides and benzophenone O-glycosides from the roots of Polygala tricornis J Nat Prod 68 2005 1802 1804
    • (2005) J Nat Prod , vol.68 , pp. 1802-1804
    • Li, J.1    Jiang, Y.2    Tu, P.F.3
  • 12
    • 77951880056 scopus 로고    scopus 로고
    • Icariin attenuates lipopolysaccharide-induced microglial activation and resultant death of neurons by inhibiting TAK1/IKK/NF-κB and JNK/p38 MAPK pathways
    • K.W. Zeng, H. Fu, G.X. Liu, and X.M. Wang Icariin attenuates lipopolysaccharide-induced microglial activation and resultant death of neurons by inhibiting TAK1/IKK/NF-κB and JNK/p38 MAPK pathways Int Immunopharmacol 10 2010 668 678
    • (2010) Int Immunopharmacol , vol.10 , pp. 668-678
    • Zeng, K.W.1    Fu, H.2    Liu, G.X.3    Wang, X.M.4
  • 14
    • 72049083253 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of optically active α-methylene-γ- carboxy-γ-lactams and γ-lactones
    • A. Bertoli, L. Fanfoni, F. Felluga, G. Pitacco, and E. Valentin Chemoenzymatic synthesis of optically active α-methylene-γ-carboxy- γ-lactams and γ-lactones Tetrahedron: Asymmetry 20 2009 2305 2310
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 2305-2310
    • Bertoli, A.1    Fanfoni, L.2    Felluga, F.3    Pitacco, G.4    Valentin, E.5
  • 15
    • 0030598086 scopus 로고    scopus 로고
    • The asymmetric synthesis of allylglycine and other unnatural α-amino acids via Zinc-mediated allylation of oximes in aqueous media
    • S. Hanessian, and R.Y. Yang The asymmetric synthesis of allylglycine and other unnatural α-amino acids via Zinc-mediated allylation of oximes in aqueous media Tetrahedron Lett 37 1996 5273 5276
    • (1996) Tetrahedron Lett , vol.37 , pp. 5273-5276
    • Hanessian, S.1    Yang, R.Y.2
  • 16
    • 34047263655 scopus 로고    scopus 로고
    • Studies on the chemical constituents of Lonicera bournei Hemsl
    • T. Xiang, L.J. Wu, R.H. Lin, J.W. Sun, and X.B. Dai Studies on the chemical constituents of Lonicera bournei Hemsl Chin J Med Chem 9 1999 48 49
    • (1999) Chin J Med Chem , vol.9 , pp. 48-49
    • Xiang, T.1    Wu, L.J.2    Lin, R.H.3    Sun, J.W.4    Dai, X.B.5
  • 17
    • 0032807393 scopus 로고    scopus 로고
    • Tuliposides from Tulipa sylvestris and T. turkestanica
    • L.P. Christensen Tuliposides from Tulipa sylvestris and T. turkestanica Phytochemistry 51 1999 969 974
    • (1999) Phytochemistry , vol.51 , pp. 969-974
    • Christensen, L.P.1
  • 19
    • 0042883925 scopus 로고    scopus 로고
    • Study on the phenolic acid constituents from Chinese medicine Shen Ma, rhizome of Cimicifuga foetida L
    • X.H. Zhao, D.H. Chen, J.Y. Si, R.L. Pan, and L.G. Shen Study on the phenolic acid constituents from Chinese medicine Shen Ma, rhizome of Cimicifuga foetida L Acta Pharmacol Sin 37 2002 535 538
    • (2002) Acta Pharmacol Sin , vol.37 , pp. 535-538
    • Zhao, X.H.1    Chen, D.H.2    Si, J.Y.3    Pan, R.L.4    Shen, L.G.5
  • 20
    • 0005550766 scopus 로고    scopus 로고
    • Isolation of a new cerebroside from the root bark of Aralia elata
    • S.S. Kang, J.S. Kim, Y.N. Xu, and Y.H. Kim Isolation of a new cerebroside from the root bark of Aralia elata J Nat Prod 62 1999 1059 1060
    • (1999) J Nat Prod , vol.62 , pp. 1059-1060
    • Kang, S.S.1    Kim, J.S.2    Xu, Y.N.3    Kim, Y.H.4
  • 21
    • 84856053860 scopus 로고    scopus 로고
    • Nitric oxide in neurodegeneration: Potential benefits of non-steroidal anti-inflammatories
    • G.H. Doherty Nitric oxide in neurodegeneration: potential benefits of non-steroidal anti-inflammatories Neurosci Bull 27 2011 366 382
    • (2011) Neurosci Bull , vol.27 , pp. 366-382
    • Doherty, G.H.1
  • 22
    • 80054071903 scopus 로고    scopus 로고
    • Perspectives on sesquiterpene lactones in inflammation and cancer
    • I. Merfort Perspectives on sesquiterpene lactones in inflammation and cancer Curr Drug Targets 12 2011 1560 1573
    • (2011) Curr Drug Targets , vol.12 , pp. 1560-1573
    • Merfort, I.1
  • 23
    • 18444367100 scopus 로고    scopus 로고
    • Anti-cancer potential of sesquiterpene lactones: Bioactivity and molecular mechanisms
    • S. Zhang, Y.K. Won, C.N. Ong, and H.M. Shen Anti-cancer potential of sesquiterpene lactones: bioactivity and molecular mechanisms Curr Med Chem Anticancer Agents 5 2005 239 249
    • (2005) Curr Med Chem Anticancer Agents , vol.5 , pp. 239-249
    • Zhang, S.1    Won, Y.K.2    Ong, C.N.3    Shen, H.M.4
  • 25
    • 34548440263 scopus 로고    scopus 로고
    • The chemical constituents of Polygala hongkongensis Hemsl
    • J.F. Wu, S.B. Chen, S.L. Chen, and P.F. Tu The chemical constituents of Polygala hongkongensis Hemsl Acta Pharmacol Sin 42 2007 757 761
    • (2007) Acta Pharmacol Sin , vol.42 , pp. 757-761
    • Wu, J.F.1    Chen, S.B.2    Chen, S.L.3    Tu, P.F.4
  • 26
    • 78449293371 scopus 로고    scopus 로고
    • One-pot synthesis of chiral a-methylene-y-lactams with excellent diastereoselectivities and enantioselectivities
    • A. Shen, M. Liu, Z.S. Jia, M.H. Xu, and G.Q. Lin One-pot synthesis of chiral a-methylene-y-lactams with excellent diastereoselectivities and enantioselectivities Org Lett 12 2010 5154 5157
    • (2010) Org Lett , vol.12 , pp. 5154-5157
    • Shen, A.1    Liu, M.2    Jia, Z.S.3    Xu, M.H.4    Lin, G.Q.5
  • 28
    • 79952850475 scopus 로고    scopus 로고
    • Novel methodologies for the synthesis of functhionalized pyroglutamates
    • S. Tekkam, M.A. Alam, S.C. Jonnalagadda, and V.R. Mereddy Novel methodologies for the synthesis of functhionalized pyroglutamates Chem Commun 47 2011 3219 3221
    • (2011) Chem Commun , vol.47 , pp. 3219-3221
    • Tekkam, S.1    Alam, M.A.2    Jonnalagadda, S.C.3    Mereddy, V.R.4
  • 29
    • 77950350288 scopus 로고    scopus 로고
    • A convenient synthesis and cytotoxic evaluation of β-aryl-α- methylidene-γ-lactones and β-aryl-α-methylidene-γ-lactams
    • A. Albrecht, Ł. Albrecht, M. Różalski, U. Krajewska, A. Janecka, and K. Studzian A convenient synthesis and cytotoxic evaluation of β-aryl-α-methylidene-γ-lactones and β-aryl-α- methylidene-γ-lactams New J Chem 34 2010 750 761
    • (2010) New J Chem , vol.34 , pp. 750-761
    • Albrecht, A.1    Albrecht, Ł.2    Rózalski, M.3    Krajewska, U.4    Janecka, A.5    Studzian, K.6
  • 30
    • 80052828625 scopus 로고    scopus 로고
    • A convenient synthesis of functionalized α-methylidenebutano-4- lactams
    • G. Liberge, S. Lebrum, A. Couture, and P. Grandclaudon A convenient synthesis of functionalized α-methylidenebutano-4-lactams Helv Chim Acta 94 2011 1662 1670
    • (2011) Helv Chim Acta , vol.94 , pp. 1662-1670
    • Liberge, G.1    Lebrum, S.2    Couture, A.3    Grandclaudon, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.