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Volumn 114, Issue 4, 2009, Pages 1316-1320

Biguaiascorzolides A and B: Two novel dimeric guaianolides with a rare skeleton, from Scorzonera austriaca

Author keywords

Asteraceae; Cytotoxicity; Dimeric sesquiterpenoid; Scorzonera austriaca

Indexed keywords

ANTINEOPLASTIC AGENT; BIGUAIASCORZOLIDE A; BIGUAIASCORZOLIDE B; CARBON; DOXORUBICIN; GUAIANOLIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 60249092437     PISSN: 03088146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.foodchem.2008.11.009     Document Type: Article
Times cited : (38)

References (27)
  • 3
    • 0030471908 scopus 로고    scopus 로고
    • Four new sesquiterpene polyol esters from Cremanthodium ellisii
    • Chen H., Zhu Y., Shen X.-M., and Jia Z.-J. Four new sesquiterpene polyol esters from Cremanthodium ellisii. Journal of Natural Products 59 12 (1996) 1117-1120
    • (1996) Journal of Natural Products , vol.59 , Issue.12 , pp. 1117-1120
    • Chen, H.1    Zhu, Y.2    Shen, X.-M.3    Jia, Z.-J.4
  • 4
    • 2642583062 scopus 로고    scopus 로고
    • Cytotoxic and pro-apoptotic activities of cynaropicrin, a sesquiterpene lactone, on the viability of leukocyte cancer cell lines
    • Cho J.Y., Kim A.R., Jung J.H., Chun T., Rhee M.H., and Yoo E.S. Cytotoxic and pro-apoptotic activities of cynaropicrin, a sesquiterpene lactone, on the viability of leukocyte cancer cell lines. European Journal of Pharmacology 492 2 (2004) 85-94
    • (2004) European Journal of Pharmacology , vol.492 , Issue.2 , pp. 85-94
    • Cho, J.Y.1    Kim, A.R.2    Jung, J.H.3    Chun, T.4    Rhee, M.H.5    Yoo, E.S.6
  • 6
    • 19544377691 scopus 로고    scopus 로고
    • Isolation and identification of cytotoxic compounds from Bay leaf (Laurus nobilis)
    • Fang F., Sang S., Chen K.Y., Gosslau A., Ho C.-T., and Rosen R.T. Isolation and identification of cytotoxic compounds from Bay leaf (Laurus nobilis). Food Chemistry 93 3 (2005) 497-501
    • (2005) Food Chemistry , vol.93 , Issue.3 , pp. 497-501
    • Fang, F.1    Sang, S.2    Chen, K.Y.3    Gosslau, A.4    Ho, C.-T.5    Rosen, R.T.6
  • 8
    • 0033571108 scopus 로고    scopus 로고
    • The anti-inflammatory sesquiterpene lactone parthenolide inhibits NF-κB by targeting the IκB kinase complex
    • Hehner S.P., Hofmann T.G., Droge W., and Schmitz M.L. The anti-inflammatory sesquiterpene lactone parthenolide inhibits NF-κB by targeting the IκB kinase complex. Journal of Immunology 163 10 (1999) 5617-5623
    • (1999) Journal of Immunology , vol.163 , Issue.10 , pp. 5617-5623
    • Hehner, S.P.1    Hofmann, T.G.2    Droge, W.3    Schmitz, M.L.4
  • 9
    • 0027531682 scopus 로고
    • A new approach for measurement of cytotoxicity using colorimetric assay
    • Hussain R.F., Nouri A.M.E., and Oliver R.T.D. A new approach for measurement of cytotoxicity using colorimetric assay. Journal of immunological methods 160 1 (1993) 89-96
    • (1993) Journal of immunological methods , vol.160 , Issue.1 , pp. 89-96
    • Hussain, R.F.1    Nouri, A.M.E.2    Oliver, R.T.D.3
  • 11
    • 9144271206 scopus 로고    scopus 로고
    • A new sesquiterpene lactone from Scorzonera austriaca
    • Li J., Wu Q.-X., Shi Y.-P., and Zhu Y. A new sesquiterpene lactone from Scorzonera austriaca. Chinese Chemical Letters 15 11 (2004) 1309-1310
    • (2004) Chinese Chemical Letters , vol.15 , Issue.11 , pp. 1309-1310
    • Li, J.1    Wu, Q.-X.2    Shi, Y.-P.3    Zhu, Y.4
  • 12
    • 0027145917 scopus 로고
    • Potential allelopathic guaianolides from cultivar sunflower leaves, var SH-222
    • Macias F.A., Varela R.M., Torres A., and Molinillo J.M.G. Potential allelopathic guaianolides from cultivar sunflower leaves, var SH-222. Phytochemistry 34 3 (1993) 669-674
    • (1993) Phytochemistry , vol.34 , Issue.3 , pp. 669-674
    • Macias, F.A.1    Varela, R.M.2    Torres, A.3    Molinillo, J.M.G.4
  • 13
    • 33746170663 scopus 로고    scopus 로고
    • Toward the synthesis of thapsigargin: Enantioselective synthesis of 7,11-dihydroxy-guaianolides
    • Manzano F.L., Guerra F.M., Moreno-Dorado F.J., Jorge Z.D., and Massanet G.M. Toward the synthesis of thapsigargin: Enantioselective synthesis of 7,11-dihydroxy-guaianolides. Organic Letters 8 13 (2006) 2879-2882
    • (2006) Organic Letters , vol.8 , Issue.13 , pp. 2879-2882
    • Manzano, F.L.1    Guerra, F.M.2    Moreno-Dorado, F.J.3    Jorge, Z.D.4    Massanet, G.M.5
  • 14
    • 0141516214 scopus 로고    scopus 로고
    • Facile asymmetric synthesis of the core nuclei of xanthanolides, guaianolides, and eudesmanolides
    • Nosse B., Chhor R.B., Jeong W.B., Bölhm C., and Reiser O. Facile asymmetric synthesis of the core nuclei of xanthanolides, guaianolides, and eudesmanolides. Organic Letters 5 6 (2003) 941-944
    • (2003) Organic Letters , vol.5 , Issue.6 , pp. 941-944
    • Nosse, B.1    Chhor, R.B.2    Jeong, W.B.3    Bölhm, C.4    Reiser, O.5
  • 15
    • 0030988493 scopus 로고    scopus 로고
    • New guaiane metabolites from the Caribbean Gorgonian coral, Pseudopterogorgia americana
    • Rodriguez A.D., and Boulanger A. New guaiane metabolites from the Caribbean Gorgonian coral, Pseudopterogorgia americana. Journal of Natural Products 60 3 (1997) 207-211
    • (1997) Journal of Natural Products , vol.60 , Issue.3 , pp. 207-211
    • Rodriguez, A.D.1    Boulanger, A.2
  • 17
    • 34347400020 scopus 로고    scopus 로고
    • Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives
    • Scotti L., Scotti M.T., Ishiki H.M., Ferreira M.J.P., Emerenciano V.P., de S. Menezes C.M., et al. Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives. Food Chemistry 105 1 (2007) 77-83
    • (2007) Food Chemistry , vol.105 , Issue.1 , pp. 77-83
    • Scotti, L.1    Scotti, M.T.2    Ishiki, H.M.3    Ferreira, M.J.P.4    Emerenciano, V.P.5    de S. Menezes, C.M.6
  • 18
    • 60249103365 scopus 로고    scopus 로고
    • Semenov, A.A, Tolstikhina, V.V, Bryanskii, O.V, & Khobrakova, V.B, 2002, As Sibe Irkut Chem Inst ASIR-S, Patent Number: RU2178709-C2
    • Semenov, A.A., Tolstikhina, V.V., Bryanskii, O.V., & Khobrakova, V.B. (2002). As Sibe Irkut Chem Inst (ASIR-S). Patent Number: RU2178709-C2.
  • 19
    • 0038824658 scopus 로고    scopus 로고
    • Sesquiterpene lactones and other constituents from the aerial parts of Carpesium macrocephalum
    • Yang C., Zhu Y., and Jia Z.-J. Sesquiterpene lactones and other constituents from the aerial parts of Carpesium macrocephalum. Australian Journal of Chemistry 56 6 (2003) 621-624
    • (2003) Australian Journal of Chemistry , vol.56 , Issue.6 , pp. 621-624
    • Yang, C.1    Zhu, Y.2    Jia, Z.-J.3
  • 20
    • 2342452390 scopus 로고    scopus 로고
    • Five new sesquiterpenoids from Parasenecio petasitoides
    • Zhang H., Liao Z.-X., and Yue J.-M. Five new sesquiterpenoids from Parasenecio petasitoides. Helvetica Chimica Acta 87 4 (2004) 976-982
    • (2004) Helvetica Chimica Acta , vol.87 , Issue.4 , pp. 976-982
    • Zhang, H.1    Liao, Z.-X.2    Yue, J.-M.3
  • 22
    • 0001943514 scopus 로고
    • Systematics and evolution within the Compositae, seen with the eyes of a chemist
    • Zdero C., and Bohlmann F. Systematics and evolution within the Compositae, seen with the eyes of a chemist. Plant Systematics and Evolution 171 1 (1990) 1-14
    • (1990) Plant Systematics and Evolution , vol.171 , Issue.1 , pp. 1-14
    • Zdero, C.1    Bohlmann, F.2
  • 23
    • 0343090754 scopus 로고    scopus 로고
    • Sesquiterpenoids from Scorzonera hispanica
    • Zidorn C., Ellmerer-Müller E.P., and Stuppner H. Sesquiterpenoids from Scorzonera hispanica. Pharmazie 55 7 (2000) 550-555
    • (2000) Pharmazie , vol.55 , Issue.7 , pp. 550-555
    • Zidorn, C.1    Ellmerer-Müller, E.P.2    Stuppner, H.3
  • 24
    • 0346037305 scopus 로고    scopus 로고
    • Tyrolobibenzyls E and F from Scorzonera humilis and distribution of caffeic acid derivatives, lignans and tyrolobibenzyls in European taxa of the subtribe Scorzonerinae (Lactuceae, Asteraceae)
    • Zidorn C., Ellmerer E.P., Sturm S., and Stuppner H. Tyrolobibenzyls E and F from Scorzonera humilis and distribution of caffeic acid derivatives, lignans and tyrolobibenzyls in European taxa of the subtribe Scorzonerinae (Lactuceae, Asteraceae). Phytochemistry 63 1 (2003) 61-67
    • (2003) Phytochemistry , vol.63 , Issue.1 , pp. 61-67
    • Zidorn, C.1    Ellmerer, E.P.2    Sturm, S.3    Stuppner, H.4
  • 25
    • 0032709045 scopus 로고    scopus 로고
    • Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum
    • Zhu Y., Yang L., and Jia Z.-J. Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum. Journal of Natural Products 62 11 (1999) 1479-1483
    • (1999) Journal of Natural Products , vol.62 , Issue.11 , pp. 1479-1483
    • Zhu, Y.1    Yang, L.2    Jia, Z.-J.3
  • 26
    • 55249095303 scopus 로고    scopus 로고
    • Four new compounds from Sinacalia tangutica
    • Zhu Y., Zhao Y., Huang G.-D., and Wu W.-S. Four new compounds from Sinacalia tangutica. Helvetica Chimica Acta 91 10 (2008) 1894-1901
    • (2008) Helvetica Chimica Acta , vol.91 , Issue.10 , pp. 1894-1901
    • Zhu, Y.1    Zhao, Y.2    Huang, G.-D.3    Wu, W.-S.4
  • 27
    • 20644467982 scopus 로고    scopus 로고
    • Epoxide sesquiterpenes and steroids from Cremanthodium discoidem
    • Zhu Y., Zhu Q.-X., and Jia Z.-J. Epoxide sesquiterpenes and steroids from Cremanthodium discoidem. Australian Journal of Chemistry 53 10 (2000) 831-834
    • (2000) Australian Journal of Chemistry , vol.53 , Issue.10 , pp. 831-834
    • Zhu, Y.1    Zhu, Q.-X.2    Jia, Z.-J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.