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Volumn 69, Issue 1, 2008, Pages 276-287

Erratum to "Cytotoxic ent-abietane diterpenes from Gelonium aequoreum" [Phytochemistry 69 (2008) 276-287] (DOI:10.1016/j.phytochem.2007.07.005);Cytotoxic ent-abietane diterpenes from Gelonium aequoreum

Author keywords

Cytotoxicity; ent Abietane diterpenes; Euphorbiaceae; Gelomulides K X; Gelonium aequoreum

Indexed keywords

EUPHORBIA; EUPHORBIACEAE; GELONIUM;

EID: 37149040418     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2009.08.003     Document Type: Erratum
Times cited : (28)

References (17)
  • 1
    • 0000133587 scopus 로고
    • The CD of αβ-unsaturated lactones
    • Beecham A.F. The CD of αβ-unsaturated lactones. Tetrahedron 28 (1972) 5543-5554
    • (1972) Tetrahedron , vol.28 , pp. 5543-5554
    • Beecham, A.F.1
  • 2
  • 5
    • 0027597815 scopus 로고
    • Three flavone glycosides from Gelonium multiflorum
    • Das B., and Chakravarty A.K. Three flavone glycosides from Gelonium multiflorum. Phytochemistry 33 (1993) 493-496
    • (1993) Phytochemistry , vol.33 , pp. 493-496
    • Das, B.1    Chakravarty, A.K.2
  • 10
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays
    • Mosmann T. 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
    • Mosmann, T.1
  • 12
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani I., Kusumi T., Kashman Y., and Kakisawa H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 113 (1991) 4092-4096
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 13
    • 0001522408 scopus 로고
    • Luteolin 7,4′-dimethyl ether 3′-glucoside from Gelonium multiflorum
    • Parveen N., and Khan N.U. Luteolin 7,4′-dimethyl ether 3′-glucoside from Gelonium multiflorum. Phytochemistry 26 (1987) 2130-2131
    • (1987) Phytochemistry , vol.26 , pp. 2130-2131
    • Parveen, N.1    Khan, N.U.2
  • 14
    • 0000584199 scopus 로고
    • Crystalline constituents of Euphobiaceae: Part X-The triterpenes of Gelonium multiflorum bark
    • Row L.R., and Rao C.S. Crystalline constituents of Euphobiaceae: Part X-The triterpenes of Gelonium multiflorum bark. Indian J. Chem. 7 (1969) 207-209
    • (1969) Indian J. Chem. , vol.7 , pp. 207-209
    • Row, L.R.1    Rao, C.S.2
  • 15
    • 0000237220 scopus 로고
    • Terpenoids and related compounds-III: Bauerenol and multiflorenol from Gelonium multiflorum A. Juss. The structure of multiflorenol
    • Sengupta P., and Khastgir H.N. Terpenoids and related compounds-III: Bauerenol and multiflorenol from Gelonium multiflorum A. Juss. The structure of multiflorenol. Tetrahedron 19 (1963) 123-132
    • (1963) Tetrahedron , vol.19 , pp. 123-132
    • Sengupta, P.1    Khastgir, H.N.2
  • 16
    • 0000351084 scopus 로고
    • Stereostructures and molecular conformations of six diterpene lactones from Gelonium multiflorum
    • and 3581-3582
    • Talapatra S.K., Das G., and Talapatra B. Stereostructures and molecular conformations of six diterpene lactones from Gelonium multiflorum. Phytochemistry 28 (1989) 1181-1185 and 3581-3582
    • (1989) Phytochemistry , vol.28 , pp. 1181-1185
    • Talapatra, S.K.1    Das, G.2    Talapatra, B.3
  • 17
    • 0032487776 scopus 로고    scopus 로고
    • Stereostructures and conformations of four diterpene lactones from Gelonium multiflorum
    • Talapatra B., Das G., Das A.K., Biswas K., and Talapatra S.K. Stereostructures and conformations of four diterpene lactones from Gelonium multiflorum. Phytochemistry 49 (1998) 1353-1360
    • (1998) Phytochemistry , vol.49 , pp. 1353-1360
    • Talapatra, B.1    Das, G.2    Das, A.K.3    Biswas, K.4    Talapatra, S.K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.