메뉴 건너뛰기




Volumn 85, Issue 1, 2013, Pages 169-175

NO inhibitory guaianolide-derived terpenoids from Artemisia argyi

Author keywords

Absolute configuration; Artemisia argyi; Guaianolide derived terpenoid; Nitric oxide

Indexed keywords

GUAIANOLIDE DERIVATIVE; INDUCIBLE NITRIC OXIDE SYNTHASE; NITRIC OXIDE; TERPENOID DERIVATIVE;

EID: 84874730697     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2012.12.005     Document Type: Article
Times cited : (78)

References (44)
  • 2
    • 12444270043 scopus 로고    scopus 로고
    • Anti-tumor activity of the farnesyl-protein transferase inhibitors arteminolides, isolated from Artemisia
    • S.H. Lee, M.Y. Lee, H.M. Kang, D.C. Han, K.H. Son, and D.C. Yang Anti-tumor activity of the farnesyl-protein transferase inhibitors arteminolides, isolated from Artemisia Bioorg Med Chem 11 2003 4545 4549
    • (2003) Bioorg Med Chem , vol.11 , pp. 4545-4549
    • Lee, S.H.1    Lee, M.Y.2    Kang, H.M.3    Han, D.C.4    Son, K.H.5    Yang, D.C.6
  • 3
    • 84861530638 scopus 로고    scopus 로고
    • Artanomadimers A-F: Six new dimeric guaianolides from Artemisia anomala
    • K. Zan, X.Y. Chai, X.Q. Chen, Q. Wu, Q. Fu, and S.X. Zhou Artanomadimers A-F: six new dimeric guaianolides from Artemisia anomala Tetrahedron 68 2012 5060 5065
    • (2012) Tetrahedron , vol.68 , pp. 5060-5065
    • Zan, K.1    Chai, X.Y.2    Chen, X.Q.3    Wu, Q.4    Fu, Q.5    Zhou, S.X.6
  • 4
    • 76049118218 scopus 로고    scopus 로고
    • Dimeric guaianolides and sesquiterpenoids from Artemisia anomala
    • J. Wen, H.M. Shi, Z.R. Xu, H.T. Chang, C.Q. Jia, and K. Zan Dimeric guaianolides and sesquiterpenoids from Artemisia anomala J Nat Prod 73 2010 67 70
    • (2010) J Nat Prod , vol.73 , pp. 67-70
    • Wen, J.1    Shi, H.M.2    Xu, Z.R.3    Chang, H.T.4    Jia, C.Q.5    Zan, K.6
  • 5
    • 6444244955 scopus 로고    scopus 로고
    • Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisia argyi
    • S.H. Lee, H.K. Kim, J.M. Seo, H.M. Kang, J.H. Kim, and K.H. Son Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisia argyi J Org Chem 67 2002 7670 7675
    • (2002) J Org Chem , vol.67 , pp. 7670-7675
    • Lee, S.H.1    Kim, H.K.2    Seo, J.M.3    Kang, H.M.4    Kim, J.H.5    Son, K.H.6
  • 6
    • 0034733641 scopus 로고    scopus 로고
    • Sesquiterpene lactones, inhibitors of farnesyl protein transferase, isolated from the flower of Artemisia sylvatica
    • S.H. Lee, H.M. Kang, H.C. Song, H. Lee, U.C. Lee, and K.H. Son Sesquiterpene lactones, inhibitors of farnesyl protein transferase, isolated from the flower of Artemisia sylvatica Tetrahedron 56 2000 4711 4715
    • (2000) Tetrahedron , vol.56 , pp. 4711-4715
    • Lee, S.H.1    Kang, H.M.2    Song, H.C.3    Lee, H.4    Lee, U.C.5    Son, K.H.6
  • 7
    • 0032476073 scopus 로고    scopus 로고
    • Arteminolide, an inhibitor of farnesyl transferase from Artemisia sylvatica
    • S.H. Lee, M.J. Kim, S.H. Bok, H. Lee, B.M. Kwon, and J. Shin Arteminolide, an inhibitor of farnesyl transferase from Artemisia sylvatica J Org Chem 63 1998 7111 7113
    • (1998) J Org Chem , vol.63 , pp. 7111-7113
    • Lee, S.H.1    Kim, M.J.2    Bok, S.H.3    Lee, H.4    Kwon, B.M.5    Shin, J.6
  • 8
    • 4344592673 scopus 로고    scopus 로고
    • Inhibitors of the LPS-induced NF-κB activation from Artemisia sylvatica
    • H.Z. Jin, J.H. Lee, D.H. Lee, Y.S. Hong, Y.H. Kim, and J.J. Lee Inhibitors of the LPS-induced NF-κB activation from Artemisia sylvatica Phytochemistry 65 2004 2247 2253
    • (2004) Phytochemistry , vol.65 , pp. 2247-2253
    • Jin, H.Z.1    Lee, J.H.2    Lee, D.H.3    Hong, Y.S.4    Kim, Y.H.5    Lee, J.J.6
  • 9
    • 0034521383 scopus 로고    scopus 로고
    • Guaiane dimers and germacranolide from Artemisia caruifolia
    • C.M. Ma, N. Nakamura, M. Hattori, S. Zhu, and K. Komatsu Guaiane dimers and germacranolide from Artemisia caruifolia J Nat Prod 63 2000 1626 1629
    • (2000) J Nat Prod , vol.63 , pp. 1626-1629
    • Ma, C.M.1    Nakamura, N.2    Hattori, M.3    Zhu, S.4    Komatsu, K.5
  • 10
    • 84859766926 scopus 로고    scopus 로고
    • Achillinin B and C, new sesquiterpene dimers isolated from Achillea millefolium
    • Y. Li, M.C. Zhu, M.L. Zhang, Y.F. Wang, M. Dong, and Q.W. Shi Achillinin B and C, new sesquiterpene dimers isolated from Achillea millefolium Tetrahedron Lett 53 2012 2601 2603
    • (2012) Tetrahedron Lett , vol.53 , pp. 2601-2603
    • Li, Y.1    Zhu, M.C.2    Zhang, M.L.3    Wang, Y.F.4    Dong, M.5    Shi, Q.W.6
  • 11
    • 0003707008 scopus 로고
    • Shanghai Science and Technology Publishing House Shanghai
    • Jiangsu New Medical College Dictionary of traditional Chinese medicines 1986 Shanghai Science and Technology Publishing House Shanghai 559 562
    • (1986) Dictionary of Traditional Chinese Medicines , pp. 559-562
  • 12
    • 0021253920 scopus 로고
    • Studies on the constituents of Artemisia argyi LEVL. et VANT
    • A. Lao, Y. Fujimoto, and T. Tatsuno Studies on the constituents of Artemisia argyi LEVL. et VANT Chem Pharm Bull 32 1984 723 727
    • (1984) Chem Pharm Bull , vol.32 , pp. 723-727
    • Lao, A.1    Fujimoto, Y.2    Tatsuno, T.3
  • 13
    • 84874684756 scopus 로고
    • A new cycloartane triterpenes from Artemisia argyi
    • R.X. Tan, and Z.J. Jia A new cycloartane triterpenes from Artemisia argyi Chin Chem Lett 02 1992 117 118
    • (1992) Chin Chem Lett , vol.2 , pp. 117-118
    • Tan, R.X.1    Jia, Z.J.2
  • 14
    • 0029804702 scopus 로고    scopus 로고
    • Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese moxa, the processed leaves of Artemisia argyi Levl et Vant: Moxartenone and moxartenolide
    • M. Yoshikawa, H. Shimada, H. Matsuda, J. Yamahara, and N. Murakami Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese moxa, the processed leaves of Artemisia argyi Levl et Vant: Moxartenone and moxartenolide Chem Pharm Bull 44 1996 1656 1662
    • (1996) Chem Pharm Bull , vol.44 , pp. 1656-1662
    • Yoshikawa, M.1    Shimada, H.2    Matsuda, H.3    Yamahara, J.4    Murakami, N.5
  • 15
    • 0037179188 scopus 로고    scopus 로고
    • New sesquiterpene-monoterpene lactone, artemisolide, isolated from Artemisia argyi
    • J.H. Kim, H.K. Kim, S.B. Jeon, K.H. Son, E.H. Kim, and S.K. Kang New sesquiterpene-monoterpene lactone, artemisolide, isolated from Artemisia argyi Tetrahedron Lett 43 2002 6205 6208
    • (2002) Tetrahedron Lett , vol.43 , pp. 6205-6208
    • Kim, J.H.1    Kim, H.K.2    Jeon, S.B.3    Son, K.H.4    Kim, E.H.5    Kang, S.K.6
  • 16
  • 17
    • 0033863808 scopus 로고    scopus 로고
    • Antimutagens in gaiyou (Artemisia argyi Levl. et Vant.)
    • T. Nakasugi, M. Nakashima, and K. Komai Antimutagens in gaiyou (Artemisia argyi Levl. et Vant.) J Agric Food Chem 48 2000 3256 3266
    • (2000) J Agric Food Chem , vol.48 , pp. 3256-3266
    • Nakasugi, T.1    Nakashima, M.2    Komai, K.3
  • 18
    • 84874702454 scopus 로고    scopus 로고
    • Tripos Associates Inc. St. Louis, MO
    • Sybyl software, version X 1.1 2010 Tripos Associates Inc. St. Louis, MO
    • (2010) Sybyl Software, Version X 1.1
  • 21
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • T. Mosumann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J Immunol Methods 65 1983 55 63
    • (1983) J Immunol Methods , vol.65 , pp. 55-63
    • Mosumann, T.1
  • 22
    • 0023130372 scopus 로고
    • Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing
    • J. Carmichael, W.G. DeGraff, A.F. Gazdar, J.D. Minna, and J.B. Mitchell Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing Cancer Res 47 1987 936 942
    • (1987) Cancer Res , vol.47 , pp. 936-942
    • Carmichael, J.1    Degraff, W.G.2    Gazdar, A.F.3    Minna, J.D.4    Mitchell, J.B.5
  • 24
    • 0024374724 scopus 로고
    • Appraisal of the MTT assay as a rapid of chemosensitivity in acute myeloid leukaemia
    • J.M. Sargent, and C.G. Taylor Appraisal of the MTT assay as a rapid of chemosensitivity in acute myeloid leukaemia Br J Cancer 60 1989 206 210
    • (1989) Br J Cancer , vol.60 , pp. 206-210
    • Sargent, J.M.1    Taylor, C.G.2
  • 25
    • 0036180639 scopus 로고    scopus 로고
    • Choosing the best pulse sequences, acquisition parameters, postacquisition processing strategies, and probes for natural product structure elucidation by NMR Spectroscopy
    • F.R. William, and G.E. Raúl Choosing the best pulse sequences, acquisition parameters, postacquisition processing strategies, and probes for natural product structure elucidation by NMR Spectroscopy J Nat Prod 65 2002 221 244
    • (2002) J Nat Prod , vol.65 , pp. 221-244
    • William, F.R.1    Raúl, G.E.2
  • 26
    • 0000404107 scopus 로고
    • A eudesmanolide and other constituents from Inula graveolens
    • S. Öksüz, and G. Topçu A eudesmanolide and other constituents from Inula graveolens Phytochemistry 31 1992 195 197
    • (1992) Phytochemistry , vol.31 , pp. 195-197
    • Öksüz, S.1    Topçu, G.2
  • 27
    • 43749113808 scopus 로고    scopus 로고
    • Stereochemistry and conformations of natural 1, 2-epoxy-guaianolides based on 1D and 2D NMR data and semiempirical calculations
    • S. Trifunović, S. Milosavljević, V. Vajs, S. Macura, and N. Todorović Stereochemistry and conformations of natural 1, 2-epoxy-guaianolides based on 1D and 2D NMR data and semiempirical calculations Magn Reson Chem 46 2008 427 431
    • (2008) Magn Reson Chem , vol.46 , pp. 427-431
    • Trifunović, S.1    Milosavljević, S.2    Vajs, V.3    MacUra, S.4    Todorović, N.5
  • 28
    • 0013582936 scopus 로고
    • Sesquiterpene lactones from Artemisia Herba-Alba
    • J.F. Sanz, G. Castellano, and J.A. Marco Sesquiterpene lactones from Artemisia Herba-Alba Phytochemistry 29 1990 541 545
    • (1990) Phytochemistry , vol.29 , pp. 541-545
    • Sanz, J.F.1    Castellano, G.2    Marco, J.A.3
  • 30
    • 49849117380 scopus 로고
    • Circular dichroism and optical rotatory dispersion of sesquiterpene lactones
    • W. Stocklin, T.G. Waddell, and T.A. Geissman Circular dichroism and optical rotatory dispersion of sesquiterpene lactones Tetrahedron 26 1970 2397 2409
    • (1970) Tetrahedron , vol.26 , pp. 2397-2409
    • Stocklin, W.1    Waddell, T.G.2    Geissman, T.A.3
  • 31
    • 0030062547 scopus 로고    scopus 로고
    • Circular dichroism of C-7, C-6 trans-fused guaianolides of Centaurea scoparia
    • D. Youssef, and A.W. Frahm Circular dichroism of C-7, C-6 trans-fused guaianolides of Centaurea scoparia Phytochemistry 41 1996 1107 1111
    • (1996) Phytochemistry , vol.41 , pp. 1107-1111
    • Youssef, D.1    Frahm, A.W.2
  • 32
    • 78649918714 scopus 로고    scopus 로고
    • Determination of absolute configuration of natural products: Theoretical calculation of electronic circular dichroism as a tool
    • X.C. Li, D. Ferreira, and Y.Q. Ding Determination of absolute configuration of natural products: theoretical calculation of electronic circular dichroism as a tool Curr Org Chem 14 2010 1678 1697
    • (2010) Curr Org Chem , vol.14 , pp. 1678-1697
    • Li, X.C.1    Ferreira, D.2    Ding, Y.Q.3
  • 33
    • 0027024178 scopus 로고
    • Chemical studies on essential oils from Artemisia species
    • J.G. Pan, Z.L. Xu, and L. Ji Chemical studies on essential oils from Artemisia species Chin J Chin Mater Med 17 1992 741 744
    • (1992) Chin J Chin Mater Med , vol.17 , pp. 741-744
    • Pan, J.G.1    Xu, Z.L.2    Ji, L.3
  • 34
    • 84874704548 scopus 로고    scopus 로고
    • Comparison of the chemical composition of volatile oils of Qi'ai, Bei'ai, and Chuan'ai
    • Y.G. Zong, X.L. Yu, and Y.Q. Chen Comparison of the chemical composition of volatile oils of Qi'ai, Bei'ai, and Chuan'ai Chin Tradit Herb Drugs 27 1996 138 140
    • (1996) Chin Tradit Herb Drugs , vol.27 , pp. 138-140
    • Zong, Y.G.1    Yu, X.L.2    Chen, Y.Q.3
  • 35
    • 0036241803 scopus 로고    scopus 로고
    • Dimeric guaianolides and a fulvenoguaianolide from Artemisia myriantha
    • H.F. Wong, D. Geoffrey, and G.D. Brown Dimeric guaianolides and a fulvenoguaianolide from Artemisia myriantha J Nat Prod 65 2002 481 486
    • (2002) J Nat Prod , vol.65 , pp. 481-486
    • Wong, H.F.1    Geoffrey, D.2    Brown, G.D.3
  • 37
    • 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
  • 38
    • 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
  • 39
    • 0031809547 scopus 로고    scopus 로고
    • The role of nitric oxide in inflammation and immunity
    • R.M. Clancy, A.R. Amin, and S.B. Abramson The role of nitric oxide in inflammation and immunity Arthritis Rheum 41 1998 1141 1151
    • (1998) Arthritis Rheum , vol.41 , pp. 1141-1151
    • Clancy, R.M.1    Amin, A.R.2    Abramson, S.B.3
  • 40
    • 0036229078 scopus 로고    scopus 로고
    • Role of nitric oxide in inflammatory conditions
    • R.C. Blantz, and K. Munger Role of nitric oxide in inflammatory conditions Nephron 90 2002 373 378
    • (2002) Nephron , vol.90 , pp. 373-378
    • Blantz, R.C.1    Munger, K.2
  • 42
    • 0032838699 scopus 로고    scopus 로고
    • Quantitative structure-cytotoxicity relationships within a series of helenanolide type sesquiterpene lactones
    • T.J. Schmidt Quantitative structure-cytotoxicity relationships within a series of helenanolide type sesquiterpene lactones Pharm Pharmacol Lett 9 1999 9 13
    • (1999) Pharm Pharmacol Lett , vol.9 , pp. 9-13
    • Schmidt, T.J.1
  • 44
    • 34547754038 scopus 로고    scopus 로고
    • Artemisolide is a typical inhibitor of IκB kinase β targeting cysteine-179 residue and down-regulates NF-κB-dependent TNF-α expression in LPS-activated macrophages
    • B.H. Kim, J.Y. Lee, J.H. Seo, H.Y. Lee, S.Y. Ryu, and B.W. Ahn Artemisolide is a typical inhibitor of IκB kinase β targeting cysteine-179 residue and down-regulates NF-κB-dependent TNF-α expression in LPS-activated macrophages Biochem Biophys Res Commun 361 2007 593 598
    • (2007) Biochem Biophys Res Commun , vol.361 , pp. 593-598
    • Kim, B.H.1    Lee, J.Y.2    Seo, J.H.3    Lee, H.Y.4    Ryu, S.Y.5    Ahn, B.W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.