메뉴 건너뛰기




Volumn 86, Issue , 2013, Pages 159-167

Tetracyclic triterpenoids and terpenylated coumarins from the bark of Ailanthus altissima ("Tree of Heaven")

Author keywords

Ailanthus altissima; Altissimanins; Atissimacoumarins; Cytotoxicities; Simaroubaceae; Triterpenoids

Indexed keywords

COUMARIN DERIVATIVE; TRITERPENE;

EID: 84872046234     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2012.10.008     Document Type: Article
Times cited : (58)

References (37)
  • 1
    • 0017387878 scopus 로고
    • 13C NMR study of ginseng sapogenins and their related dammarane type triterpenes
    • 13C NMR study of ginseng sapogenins and their related dammarane type triterpenes Tetrahedron 33 1977 1935 1939
    • (1977) Tetrahedron , vol.33 , pp. 1935-1939
    • Asakawa, J.1    Kasai, R.2    Yamasaki, K.3    Tanaka, O.4
  • 2
    • 37049092829 scopus 로고
    • Triterpenoids of Aglaia odorata. Configuration of trisubstituted epoxides
    • R.B. Boar, and K. Damps Triterpenoids of Aglaia odorata. Configuration of trisubstituted epoxides J. Chem. Soc., Perkin Trans. 1 1977 510 512
    • (1977) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 510-512
    • Boar, R.B.1    Damps, K.2
  • 3
    • 0036273674 scopus 로고    scopus 로고
    • Interference of plant extracts, phytoestrogens and antioxidants with the MTT tetrazolium assay
    • R. Bruggisser, K. von Daeniken, G. Jundt, W. Schaffner, and H. Tullberg-Reinert Interference of plant extracts, phytoestrogens and antioxidants with the MTT tetrazolium assay Planta Med. 68 2002 445 448
    • (2002) Planta Med. , vol.68 , pp. 445-448
    • Bruggisser, R.1    Von Daeniken, K.2    Jundt, G.3    Schaffner, W.4    Tullberg-Reinert, H.5
  • 4
    • 0000635135 scopus 로고
    • Sterols and steryl glycosides from Urtica dioica
    • N. Chaurasia, and M. Wichtl Sterols and steryl glycosides from Urtica dioica J. Nat. Prod. 50 1987 881 885
    • (1987) J. Nat. Prod. , vol.50 , pp. 881-885
    • Chaurasia, N.1    Wichtl, M.2
  • 5
    • 0034805328 scopus 로고    scopus 로고
    • A bioassay using the human hepatoblastoma cell line HepG2 for detecting phototoxicity of furocoumarins
    • M. Colombain, V. Goll, F. Muyard, C. Girard, F. Bévalot, and L. Richert A bioassay using the human hepatoblastoma cell line HepG2 for detecting phototoxicity of furocoumarins Planta Med. 67 2001 644 646
    • (2001) Planta Med. , vol.67 , pp. 644-646
    • Colombain, M.1    Goll, V.2    Muyard, F.3    Girard, C.4    Bévalot, F.5    Richert, L.6
  • 7
    • 0037467088 scopus 로고    scopus 로고
    • Isolation of phytotoxic compounds from tree-of-heaven (Ailanthus altissima Swingle)
    • V. De Feo, L. De Martino, E. Quaranta, and C. Pizza Isolation of phytotoxic compounds from tree-of-heaven (Ailanthus altissima Swingle) J. Agric. Food Chem. 51 2003 1177 1180
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 1177-1180
    • De Feo, V.1    De Martino, L.2    Quaranta, E.3    Pizza, C.4
  • 9
    • 0031031683 scopus 로고    scopus 로고
    • Antitumor Agents. 168. Dysoxylum cumingianum. IV. The structures of cumingianosides G-O, new triterpene glucosides with a 14, 18- cycloapotirucallane-type skeleton from Dysoxylum cumingianum, and their cytotoxicity against human cancer cell lines
    • T. Fujioka, A. Sakurai, K. Mihashi, Y. Kashiwada, I.-S. Chen, and K.-H. Lee Antitumor Agents. 168. Dysoxylum cumingianum. IV. The structures of cumingianosides G-O, new triterpene glucosides with a 14, 18- cycloapotirucallane-type skeleton from Dysoxylum cumingianum, and their cytotoxicity against human cancer cell lines Chem. Pharm. Bull. 45 1997 68 74
    • (1997) Chem. Pharm. Bull. , vol.45 , pp. 68-74
    • Fujioka, T.1    Sakurai, A.2    Mihashi, K.3    Kashiwada, Y.4    Chen, I.-S.5    Lee, K.-H.6
  • 11
    • 0026693054 scopus 로고
    • Cytotoxic quassinoids and tirucallane-type triterpenes from the woods of Eurycoma longifolia
    • H. Itokawa, E. Kishi, H. Morita, and K. Takeya Cytotoxic quassinoids and tirucallane-type triterpenes from the woods of Eurycoma longifolia Chem. Pharm. Bull. 40 1992 1053 1055
    • (1992) Chem. Pharm. Bull. , vol.40 , pp. 1053-1055
    • Itokawa, H.1    Kishi, E.2    Morita, H.3    Takeya, K.4
  • 12
    • 0003707008 scopus 로고
    • Jiangsu New Medical College, Shanghai Science and Technology Press Shanghai
    • Jiangsu New Medical College A Dictionary of the Traditional Chinese Medicine 1986 Shanghai Science and Technology Press Shanghai p. 1891
    • (1986) A Dictionary of the Traditional Chinese Medicine , pp. 1891
  • 13
    • 0029790227 scopus 로고    scopus 로고
    • Two new quassinoids, ailantinols A and B, and related compounds from Ailanthus altissima
    • K. Kubota, N. Fukamiya, T. Hamada, M. Okano, K. Tagahara, and K.-H. Lee Two new quassinoids, ailantinols A and B, and related compounds from Ailanthus altissima J. Nat. Prod. 59 1996 683 686
    • (1996) J. Nat. Prod. , vol.59 , pp. 683-686
    • Kubota, K.1    Fukamiya, N.2    Hamada, T.3    Okano, M.4    Tagahara, K.5    Lee, K.-H.6
  • 14
    • 77956343108 scopus 로고    scopus 로고
    • A brief resume on the genus Ailanthus: Chemical and pharmacological aspects
    • P. Kundu, and S. Laskar A brief resume on the genus Ailanthus: chemical and pharmacological aspects Phytochem. Rev. 9 2010 379 412
    • (2010) Phytochem. Rev. , vol.9 , pp. 379-412
    • Kundu, P.1    Laskar, S.2
  • 16
    • 33746049186 scopus 로고    scopus 로고
    • Tirucallane triterpenes from the roots of Ozoroa insigni
    • Y. Liu, and P. Abreu Tirucallane triterpenes from the roots of Ozoroa insigni Phytochemistry 67 2006 1309 1315
    • (2006) Phytochemistry , vol.67 , pp. 1309-1315
    • Liu, Y.1    Abreu, P.2
  • 17
    • 0034739102 scopus 로고    scopus 로고
    • Tirucallane triterpenoids from Dysoxylum hainanense
    • X.-D. Luo, S.-H. Wu, Y.-B. Ma, and D.-G. Wu Tirucallane triterpenoids from Dysoxylum hainanense Phytochemistry 54 2000 801 805
    • (2000) Phytochemistry , vol.54 , pp. 801-805
    • Luo, X.-D.1    Wu, S.-H.2    Ma, Y.-B.3    Wu, D.-G.4
  • 18
    • 0031500219 scopus 로고    scopus 로고
    • Tirucallane-type triterpenoids: NMR and X-ray diffraction analyses of 24-epi-piscidinol A and piscidinol A
    • J.D. McChesney, J. Dou, R.D. Sindelar, D.K. Goins, L.A. Walker, and R.D. Rogers Tirucallane-type triterpenoids: NMR and X-ray diffraction analyses of 24-epi-piscidinol A and piscidinol A J. Chem. Crystallogr. 27 1997 283 290
    • (1997) J. Chem. Crystallogr. , vol.27 , pp. 283-290
    • McChesney, J.D.1    Dou, J.2    Sindelar, R.D.3    Goins, D.K.4    Walker, L.A.5    Rogers, R.D.6
  • 23
    • 34250204486 scopus 로고    scopus 로고
    • Structural revision of terpenoids with a (3Z)-2-methyl-3-penten-2-ol moiety by the synthesis of (23E)- and (23Z)-cycloart-23-ene-3β, 25-diols
    • S. Takahashi, H. Satoh, Y. Hongo, and H. Koshino Structural revision of terpenoids with a (3Z)-2-methyl-3-penten-2-ol moiety by the synthesis of (23E)- and (23Z)-cycloart-23-ene-3β, 25-diols J. Org. Chem. 72 2007 4578 4581
    • (2007) J. Org. Chem. , vol.72 , pp. 4578-4581
    • Takahashi, S.1    Satoh, H.2    Hongo, Y.3    Koshino, H.4
  • 24
    • 79952303577 scopus 로고    scopus 로고
    • Cycloartane triterpenes isolated from Combretum quadrangulare in a screening program for death-receptor expression enhancing activity
    • K. Toume, T. Nakazawa, T. Ohtsuki, M.A. Arai, T. Koyano, T. Kowithayakorn, and M. Ishibashi Cycloartane triterpenes isolated from Combretum quadrangulare in a screening program for death-receptor expression enhancing activity J. Nat. Prod. 74 2011 249 255
    • (2011) J. Nat. Prod. , vol.74 , pp. 249-255
    • Toume, K.1    Nakazawa, T.2    Ohtsuki, T.3    Arai, M.A.4    Koyano, T.5    Kowithayakorn, T.6    Ishibashi, M.7
  • 25
    • 0344118213 scopus 로고    scopus 로고
    • Sunpollenol and five other rearranged 3,4-seco-tirucallane-type triterpenoids from sunflower pollen and their inhibitory effects on Epstein-Barr virus activation
    • M. Ukiya, T. Akihisa, H. Tokuda, K. Koike, Y. Kimura, T. Asano, S. Motohashi, T. Nikaido, and H. Nishino Sunpollenol and five other rearranged 3,4-seco-tirucallane-type triterpenoids from sunflower pollen and their inhibitory effects on Epstein-Barr virus activation J. Nat. Prod. 66 2003 1476 1479
    • (2003) J. Nat. Prod. , vol.66 , pp. 1476-1479
    • Ukiya, M.1    Akihisa, T.2    Tokuda, H.3    Koike, K.4    Kimura, Y.5    Asano, T.6    Motohashi, S.7    Nikaido, T.8    Nishino, H.9
  • 26
    • 0038070312 scopus 로고    scopus 로고
    • Isolation, structural elucidation, and inhibitory effects of terpenoid and lipid constituents from sunflower pollen on Epstein-Barr virus early antigen induced by tumor promoter, TPA
    • M. Ukiya, T. Akihisa, H. Tokuda, K. Koike, J. Takayasu, H. Okuda, Y. Kimura, T. Nikaido, and H. Nishino Isolation, structural elucidation, and inhibitory effects of terpenoid and lipid constituents from sunflower pollen on Epstein-Barr virus early antigen induced by tumor promoter, TPA J. Agric. Food Chem. 51 2003 2949 2957
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 2949-2957
    • Ukiya, M.1    Akihisa, T.2    Tokuda, H.3    Koike, K.4    Takayasu, J.5    Okuda, H.6    Kimura, Y.7    Nikaido, T.8    Nishino, H.9
  • 28
    • 84872034561 scopus 로고    scopus 로고
    • Study on chemical constituents from bark of Ailanthus altissima swingle
    • L.-F. Wang, X.-J. Wang, W.-Z. Tang, and C.-J. Yang Study on chemical constituents from bark of Ailanthus altissima swingle Food Drug 12 2010 180 183
    • (2010) Food Drug , vol.12 , pp. 180-183
    • Wang, L.-F.1    Wang, X.-J.2    Tang, W.-Z.3    Yang, C.-J.4
  • 29
    • 0038188709 scopus 로고    scopus 로고
    • Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus
    • L.-Y. Wang, N.-L. Wang, X.-S. Yao, S. Miyata, and S. Kitanaka Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus J. Nat. Prod. 66 2003 630 633
    • (2003) J. Nat. Prod. , vol.66 , pp. 630-633
    • Wang, L.-Y.1    Wang, N.-L.2    Yao, X.-S.3    Miyata, S.4    Kitanaka, S.5
  • 31
    • 4143152565 scopus 로고
    • Dammarane triterpenes from the stem bark of Commiphora dalzielii
    • P.G. Waterman, and S. Ampofo Dammarane triterpenes from the stem bark of Commiphora dalzielii Phytochemistry 24 1985 2925 2928
    • (1985) Phytochemistry , vol.24 , pp. 2925-2928
    • Waterman, P.G.1    Ampofo, S.2
  • 33
    • 78650189141 scopus 로고    scopus 로고
    • Triterpenoids and steroids from the fruits of Melia toosendan and their cytotoxic effects on two human cancer cell lines
    • S.-B. Wu, J.-J. Su, L.-H. Sun, W.-X. Wang, Y. Zhao, H. Li, S.-P. Zhang, G.-H. Dai, C.-G. Wang, and J.-F. Hu Triterpenoids and steroids from the fruits of Melia toosendan and their cytotoxic effects on two human cancer cell lines J. Nat. Prod. 73 2010 1898 1906
    • (2010) J. Nat. Prod. , vol.73 , pp. 1898-1906
    • Wu, S.-B.1    Su, J.-J.2    Sun, L.-H.3    Wang, W.-X.4    Zhao, Y.5    Li, H.6    Zhang, S.-P.7    Dai, G.-H.8    Wang, C.-G.9    Hu, J.-F.10
  • 35
    • 78651385374 scopus 로고    scopus 로고
    • Seven new dammarane triterpenes from the floral spikes of Betula platyphylla var. japonica
    • J. Xiong, M. Taniguchi, Y. Kashiwada, T. Yamagishi, and Y. Takaishi Seven new dammarane triterpenes from the floral spikes of Betula platyphylla var. japonica J. Nat. Med. 65 2011 217 223
    • (2011) J. Nat. Med. , vol.65 , pp. 217-223
    • Xiong, J.1    Taniguchi, M.2    Kashiwada, Y.3    Yamagishi, T.4    Takaishi, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.