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Volumn 71, Issue 5, 2005, Pages 452-457

Sesquiterpenes and butenolides, natural anti-HIV constituents from Litsea verticillata

Author keywords

Anti HIV activity; Bioassay directed fractionation; Butenolides; Lauraceae; Litsea verticillata; Sesquiterpenes

Indexed keywords

1,2,3,4 TETRAHYDRI 2,5 DIMETHYL 8 (1 METHYL ETHYL) 1,2 NAPHTHALENEDIOL; 4 HYDROXY 2 METHYLBUT 2 ENOLIDE; BUTENOLIDE; CHROMOLAEVANEDIONE; GREEN FLUORESCENT PROTEIN; HYDROXYDIHYDROBOVOLIDE; ISOLITSEANE A; ISOLITSEANE B; ISOLITSEANE C; LITSEABUTENOLIDE; NAPHTHALENE DERIVATIVE; OXYPHYLLENODIOL B; PLANT EXTRACT; SESQUITERPENE; UNCLASSIFIED DRUG;

EID: 20544439638     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-864142     Document Type: Article
Times cited : (56)

References (19)
  • 1
    • 0036484293 scopus 로고    scopus 로고
    • Natural anti-HIV agents. Part I. (+)-Demethoxyepiexcelsin and verticillatol from Litsea verticillata
    • Hoang VD, Tan GT, Zhang HJ, Tamez PA, Hung NV, Cuong NM et al. Natural anti-HIV agents. Part I. (+)-Demethoxyepiexcelsin and verticillatol from Litsea verticillata. Phytochemistry 2002; 59: 325-9
    • (2002) Phytochemistry , vol.59 , pp. 325-329
    • Hoang, V.D.1    Tan, G.T.2    Zhang, H.J.3    Tamez, P.A.4    Hung, N.V.5    Cuong, N.M.6
  • 2
    • 0035802989 scopus 로고    scopus 로고
    • Natural anti-HIV agents. Part II. Litseaverticillol A, a prototypic litseane sesquiterpene from Litsea verticillata
    • Zhang HJ, Tan GT, Hoang VD, Hung NV, Cuong NM, Soejarto DD et al. Natural anti-HIV agents. Part II. Litseaverticillol A, a prototypic litseane sesquiterpene from Litsea verticillata. Tetrahedron Lett 2001; 42: 8587-91
    • (2001) Tetrahedron Lett , vol.42 , pp. 8587-8591
    • Zhang, H.J.1    Tan, G.T.2    Hoang, V.D.3    Hung, N.V.4    Cuong, N.M.5    Soejarto, D.D.6
  • 3
    • 0037421140 scopus 로고    scopus 로고
    • Natural anti-HIV agents. Part III. Litseaverticillols A-H, novel sesquiterpenes from Litsea verticillata
    • Zhang HJ, Tan GT, Hoang VD, Hung NV, Cuong NM, Soejarto DD et al. Natural anti-HIV agents. Part III. Litseaverticillols A-H, novel sesquiterpenes from Litsea verticillata. Tetrahedron 2003; 59: 141-8
    • (2003) Tetrahedron , vol.59 , pp. 141-148
    • Zhang, H.J.1    Tan, G.T.2    Hoang, V.D.3    Hung, N.V.4    Cuong, N.M.5    Soejarto, D.D.6
  • 6
    • 0024578841 scopus 로고
    • New soluble-formazan assay for HIV-1 cytopathic effects: Application to high-flux screening of synthetic and natural products for AIDS-antiviral activity
    • Weislow OS, Kiser R, Fine DL, Bader J, Shoemaker RH, Boyd MR. New soluble-formazan assay for HIV-1 cytopathic effects: application to high-flux screening of synthetic and natural products for AIDS-antiviral activity. J National Cancer Inst 1989; 81: 577-86
    • (1989) J National Cancer Inst , vol.81 , pp. 577-586
    • Weislow, O.S.1    Kiser, R.2    Fine, D.L.3    Bader, J.4    Shoemaker, R.H.5    Boyd, M.R.6
  • 7
    • 0035921092 scopus 로고    scopus 로고
    • Absolute stereostructures of novel norcadinane- and trinoreudesmane-type sesquiterpenes with nitric oxide production inhibitory activity from Alpinia oxyphylla
    • Muraoka O, Fujimoto M, Tanabe G, Kubo M, Minematsu T, Matsuda H et al. Absolute stereostructures of novel norcadinane- and trinoreudesmane-type sesquiterpenes with nitric oxide production inhibitory activity from Alpinia oxyphylla. Bioorg & Med Chem Lett 2001; 11: 2217-20
    • (2001) Bioorg & Med Chem Lett , vol.11 , pp. 2217-2220
    • Muraoka, O.1    Fujimoto, M.2    Tanabe, G.3    Kubo, M.4    Minematsu, T.5    Matsuda, H.6
  • 8
    • 0032765649 scopus 로고    scopus 로고
    • Four new sesquiterpenes from the heartwood of Juniperus formosono var. concolor
    • Kuo YH, Yu MT. Four new sesquiterpenes from the heartwood of Juniperus formosono var. concolor. Chem Pharm Bull 1999; 47: 1017-9
    • (1999) Chem Pharm Bull , vol.47 , pp. 1017-1019
    • Kuo, Y.H.1    Yu, M.T.2
  • 9
    • 0002255669 scopus 로고
    • Isodaucane derivatives, norsesquiterpenes and clerodanes from Chromolaena laevigata
    • Misra LN, Jakupovic J, Bohlmann F, Schmeda-Hirschmann G. Isodaucane derivatives, norsesquiterpenes and clerodanes from Chromolaena laevigata. Tetrahedron 1985; 41: 5353-6
    • (1985) Tetrahedron , vol.41 , pp. 5353-5356
    • Misra, L.N.1    Jakupovic, J.2    Bohlmann, F.3    Schmeda-Hirschmann, G.4
  • 10
    • 0035681444 scopus 로고    scopus 로고
    • Chemical constituents from Alseodaphne andersonii
    • Lee SS, Chang SM, Chen CH. Chemical constituents from Alseodaphne andersonii. J Nat Prod 2001; 64: 548-51
    • (2001) J Nat Prod , vol.64 , pp. 548-551
    • Lee, S.S.1    Chang, S.M.2    Ch, C.3
  • 11
    • 0016732106 scopus 로고
    • Isolation and structure of obtusilactone
    • Niwa M, Iguchi M, Yamamura S. Isolation and structure of obtusilactone. Tetrahedron Lett 1975; 16: 1539-42
    • (1975) Tetrahedron Lett , vol.16 , pp. 1539-1542
    • Niwa, M.1    Iguchi, M.2    Yamamura, S.3
  • 12
    • 20544472594 scopus 로고
    • Preparation of butenolide derivatives as intermediates for perfumes and biologically active compounds (Japan)
    • JP2218672: 5 pp
    • Takabe K, Yoda H, Tanaka M, Sugimoto M, Ishioka T, Miyazaki A. Preparation of butenolide derivatives as intermediates for perfumes and biologically active compounds (Japan). Jap Kokai Tokkyo Koho 1990; JP2218672: 5 pp
    • (1990) Jap Kokai Tokkyo Koho
    • Takabe, K.1    Yoda, H.2    Tanaka, M.3    Sugimoto, M.4    Ishioka, T.5    Miyazaki, A.6
  • 14
    • 0030525624 scopus 로고    scopus 로고
    • Secretion of allelochemicals from the cultured suspension cells of Marchantia polymorpha
    • Chen L, Izumi S, Ito DI, Iwaeda T, Utsumi R, Hirata T. Secretion of allelochemicals from the cultured suspension cells of Marchantia polymorpha. Chem Lett, 1996: 205-6
    • (1996) Chem Lett , pp. 205-206
    • Chen, L.1    Izumi, S.2    Ito, D.I.3    Iwaeda, T.4    Utsumi, R.5    Hirata, T.6
  • 16
    • 0041920812 scopus 로고    scopus 로고
    • A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative from Formosan Casearia membranacea
    • Chang KC, Duh CY, Chen IS, Tsai IL. A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative from Formosan Casearia membranacea. Planta Med 2003; 69: 667-72
    • (2003) Planta Med , vol.69 , pp. 667-672
    • Chang, K.C.1    Duh, C.Y.2    Chen, I.S.3    Tsai, I.L.4
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.