메뉴 건너뛰기




Volumn 5, Issue 2, 2012, Pages 229-232

Two new eudesmanolides from Inula racemosa and their bioactivities

Author keywords

Anti inflammation; Compositae; Cytotoxic activity; Eudesmanolide; Inula racemosa

Indexed keywords

1 ONE 4 EPI ALANTOLACTONE; 4ALPHA,13 DIHYDROXY 5,7(11) EUDESMADIEN 12,8 OLIDE; BETA GLUCURONIDASE; EUDESMANOLIDE DERIVATIVE; GINKGOLIDE B; PACLITAXEL; SESQUITERPENOID; THROMBOCYTE ACTIVATING FACTOR; UNCLASSIFIED DRUG;

EID: 84862823505     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2011.12.014     Document Type: Article
Times cited : (27)

References (14)
  • 1
    • 0021689679 scopus 로고
    • Phytochemical and biological screening of Saudi medicinal plants. Part 6. Isolation of 2α-hydroxy-alantolactone the antileukemic principle of Francoeuria crispa
    • M.A. Al-Yahya, S. Khafagy, and A. Shihata Phytochemical and biological screening of Saudi medicinal plants. Part 6. Isolation of 2α-hydroxy- alantolactone the antileukemic principle of Francoeuria crispa J. Nat. Prod. 47 1984 1013 1017
    • (1984) J. Nat. Prod. , vol.47 , pp. 1013-1017
    • Al-Yahya, M.A.1    Khafagy, S.2    Shihata, A.3
  • 3
    • 15444379017 scopus 로고    scopus 로고
    • Molecular diversity of Artocarpus champeden (Moraceae): A species endemic to Indonesia
    • E.H. Hakim, L.D. Juliawaty, Y.M. Syah, and S.A. Achmad Molecular diversity of Artocarpus champeden (Moraceae): a species endemic to Indonesia Mol. Divers. 9 2005 149 158
    • (2005) Mol. Divers. , vol.9 , pp. 149-158
    • Hakim, E.H.1    Juliawaty, L.D.2    Syah, Y.M.3    Achmad, S.A.4
  • 4
    • 0003191993 scopus 로고
    • Jiangsu New Medical College Shanghai People's Press Shanghai
    • Jiangsu New Medical College A Dictionary of Traditional Chinese Drugs 1977 Shanghai People's Press Shanghai 244 pp
    • (1977) A Dictionary of Traditional Chinese Drugs , pp. 244
  • 5
    • 84989989923 scopus 로고
    • Sesquiterpene lactones from Inula helenium
    • Y. Kashman, D. Lavie, and E. Glotter Sesquiterpene lactones from Inula helenium Israel J. Chem. 5 1967 23 27
    • (1967) Israel J. Chem. , vol.5 , pp. 23-27
    • Kashman, Y.1    Lavie, D.2    Glotter, E.3
  • 6
    • 0040615992 scopus 로고
    • Stereostructures of inunal and isoalloalantolactone, two biological active sesquiterpene lactones from Inula racemosa
    • B. Kaur, and P.S. Kalsi Stereostructures of inunal and isoalloalantolactone, two biological active sesquiterpene lactones from Inula racemosa Phytochemistry 24 1985 2007 2010
    • (1985) Phytochemistry , vol.24 , pp. 2007-2010
    • Kaur, B.1    Kalsi, P.S.2
  • 7
    • 32644440104 scopus 로고    scopus 로고
    • Five new Diels-Alder type adducts from the stem and root bark of Morus mongolica
    • J. Kang, R.Y. Chen, and D.Q. Yu Five new Diels-Alder type adducts from the stem and root bark of Morus mongolica Planta Med. 72 2006 52 59
    • (2006) Planta Med. , vol.72 , pp. 52-59
    • Kang, J.1    Chen, R.Y.2    Yu, D.Q.3
  • 8
    • 2142686115 scopus 로고    scopus 로고
    • Effect of ginkgolide B on platelet-activating factor induced activation of rat polymorphonuclear leukocytes
    • Z.G. Nie, and W.J. Wang Effect of ginkgolide B on platelet-activating factor induced activation of rat polymorphonuclear leukocytes Acta Pharm. Sinica 38 2003 98 102
    • (2003) Acta Pharm. Sinica , vol.38 , pp. 98-102
    • Nie, Z.G.1    Wang, W.J.2
  • 9
    • 33947670768 scopus 로고
    • Sesquiterpene lactones from Calea septuplinervia
    • A.G. Ober, and N.H. Fischer Sesquiterpene lactones from Calea septuplinervia Phytochemistry 26 1987 848 849
    • (1987) Phytochemistry , vol.26 , pp. 848-849
    • Ober, A.G.1    Fischer, N.H.2
  • 11
    • 0141677804 scopus 로고    scopus 로고
    • Cytotoxic sesquiterpene lactones from the root of Saussurea lappa
    • C.M. Sun, W.J. Syu, M.J. Don, J.J. Lu, and G.H. Lee Cytotoxic sesquiterpene lactones from the root of Saussurea lappa J. Nat. Prod. 66 2003 1175 1180
    • (2003) J. Nat. Prod. , vol.66 , pp. 1175-1180
    • Sun, C.M.1    Syu, W.J.2    Don, M.J.3    Lu, J.J.4    Lee, G.H.5
  • 13


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.