메뉴 건너뛰기




Volumn 74, Issue 8, 2008, Pages 870-872

Further studies of the norditerpene (+)-Harringtonolide isolated from Cephalotaxus harringtonia var. drupacea: Absolute configuration, cytotoxic and antifungal activities

Author keywords

Absolute configuration; Biological activities; Cephalotaxaceae; Cephalotaxus harringtonia var. drupacea; Norditerpenes; X ray diffraction

Indexed keywords

DITERPENE; HARRINGTONOLIDE;

EID: 47249128631     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1074546     Document Type: Article
Times cited : (62)

References (29)
  • 1
    • 0017818695 scopus 로고    scopus 로고
    • Buta JC, Flippen JL, Lusby WR. Harringtonolide, a plant growth inhibitory tropone from Cephalotaxus harringtonia (Forbes) K. Koch. J Org Chem 1978; 43: 1002-3
    • Buta JC, Flippen JL, Lusby WR. Harringtonolide, a plant growth inhibitory tropone from Cephalotaxus harringtonia (Forbes) K. Koch. J Org Chem 1978; 43: 1002-3
  • 2
    • 0010525568 scopus 로고
    • Studies on the structure of a new antitumor agent, hainanolide
    • Sun NJ, Xue Z, Liang XT, Wang L. Studies on the structure of a new antitumor agent, hainanolide. Yao Hsueh Hsueh Pao 1979; 14: 39 - 44.
    • (1979) Yao Hsueh Hsueh Pao , vol.14 , pp. 39-44
    • Sun, N.J.1    Xue, Z.2    Liang, X.T.3    Wang, L.4
  • 3
    • 0004034466 scopus 로고
    • g
    • [Chem Abstr 1980: 220590 g]
    • (1980) Chem Abstr , pp. 220590
  • 4
    • 0019547369 scopus 로고
    • Isolation and identification of the antitumor component-hainanolide from Cephalotaxus fortunei
    • Sun NJ, Zhao ZF, Chen RT, Lin W, Zhou YZ. Isolation and identification of the antitumor component-hainanolide from Cephalotaxus fortunei. Yao Hsueh Hsueh Pao 1981; 16: 233-4.
    • (1981) Yao Hsueh Hsueh Pao , vol.16 , pp. 233-234
    • Sun, N.J.1    Zhao, Z.F.2    Chen, R.T.3    Lin, W.4    Zhou, Y.Z.5
  • 5
    • 0003744531 scopus 로고
    • 156431p
    • [Chem Abstr 1981: 156431p]
    • (1981) Chem Abstr
  • 6
    • 0042852080 scopus 로고
    • Studies on the antitumor constituents of Cephalotaxus sinensis
    • Ren L, Xue Z. Studies on the antitumor constituents of Cephalotaxus sinensis. Zhongcaoyao 1981; 12: 1-4.
    • (1981) Zhongcaoyao , vol.12 , pp. 1-4
    • Ren, L.1    Xue, Z.2
  • 7
    • 0012341010 scopus 로고
    • 3672p
    • [Chem Abstr 1982: 3672p]
    • (1982) Chem Abstr
  • 9
    • 0038246179 scopus 로고
    • Antiviral effect of hainanolide
    • Kang S, Cai S, Teng L. Antiviral effect of hainanolide. Yaoxue Xuebao 1981; 16: 867 - 8.
    • (1981) Yaoxue Xuebao , vol.16 , pp. 867-868
    • Kang, S.1    Cai, S.2    Teng, L.3
  • 10
    • 0012341010 scopus 로고
    • [Chem Abstr 1982: 82519v]
    • (1982) Chem Abstr
  • 12
    • 0006053768 scopus 로고
    • [Chem Abstr 1983: 194936b]
    • (1983) Chem Abstr
  • 13
    • 3142545699 scopus 로고
    • Studies on the structure of hainanolidol
    • Xue Z, Sun NJ, Liang XT. Studies on the structure of hainanolidol. Yao Hsueh Hsueh Pao 1982; 17: 236-7.
    • (1982) Yao Hsueh Hsueh Pao , vol.17 , pp. 236-237
    • Xue, Z.1    Sun, N.J.2    Liang, X.T.3
  • 14
    • 0012341010 scopus 로고
    • [Chem Abstr 1982: 177999r]
    • (1982) Chem Abstr
  • 15
    • 0033403123 scopus 로고    scopus 로고
    • Two new lactones from Cephalotaxus fortunei var. alpina
    • Du J, Chiu MH, Nie RL. Two new lactones from Cephalotaxus fortunei var. alpina. J Nat Prod 1999; 62: 1664-5
    • (1999) J Nat Prod , vol.62 , pp. 1664-1665
    • Du, J.1    Chiu, M.H.2    Nie, R.L.3
  • 16
    • 38349081552 scopus 로고    scopus 로고
    • Yoon KD. Jeong DG, Hwang YH, Ryu JM, Kim J. Inhibitors of osteoclast differentiation from Cephalotaxus koreana. J Nat Prod 2007; 70: 2029-32
    • Yoon KD. Jeong DG, Hwang YH, Ryu JM, Kim J. Inhibitors of osteoclast differentiation from Cephalotaxus koreana. J Nat Prod 2007; 70: 2029-32
  • 19
    • 0003744531 scopus 로고
    • [Chem Abstr 1984: 59893e]
    • (1984) Chem Abstr
  • 20
    • 0032481613 scopus 로고    scopus 로고
    • Synthesis of the unusual diter-penoid tropones hainanolidol and harringtonolide
    • Frey B, Wells AP, Rogers DH, Mander LN. Synthesis of the unusual diter-penoid tropones hainanolidol and harringtonolide. J Am Chem Soc 1998; 120: 1914-5
    • (1998) J Am Chem Soc , vol.120 , pp. 1914-1915
    • Frey, B.1    Wells, A.P.2    Rogers, D.H.3    Mander, L.N.4
  • 21
    • 0000969843 scopus 로고
    • Principe et applications d'une nouvelle méthode de détermination des configurations dite "par dédoublement partiel
    • Horeau A. Principe et applications d'une nouvelle méthode de détermination des configurations dite "par dédoublement partiel". Tetrahedron Lett 1961; 15: 506-12
    • (1961) Tetrahedron Lett , vol.15 , pp. 506-512
    • Horeau, A.1
  • 22
    • 0011157358 scopus 로고
    • Détermination des configurations par "dédoublement partiel" -III- Alcools stéroíï des.
    • Horeau A, Kagan HB. Détermination des configurations par "dédoublement partiel" -III- Alcools stéroíï des. Tetrahedron 1964; 20: 2431 - 41
    • (1964) Tetrahedron , vol.20 , pp. 2431-2441
    • Horeau, A.1    Kagan, H.B.2
  • 23
    • 0029814889 scopus 로고    scopus 로고
    • Structural and stereochemical studies of C-21 terpenoids from Mediterranean Spon-giidae sponges
    • Fontana A, Albarella L, Scognamiglio G, Uriz M, Cimino G. Structural and stereochemical studies of C-21 terpenoids from Mediterranean Spon-giidae sponges. J Nat Prod 1996; 59: 869-72
    • (1996) J Nat Prod , vol.59 , pp. 869-872
    • Fontana, A.1    Albarella, L.2    Scognamiglio, G.3    Uriz, M.4    Cimino, G.5
  • 25
    • 0032893827 scopus 로고    scopus 로고
    • An example of the co-occurrence of enantiomeric labdane-type diterpenes in the leaves of Mimosa hostilis
    • Fukuyama Y, Yokoyama R, Ohsaki A, Takahashi H, Minami H. An example of the co-occurrence of enantiomeric labdane-type diterpenes in the leaves of Mimosa hostilis. Chem Pharm Bull 1999; 47: 454-5
    • (1999) Chem Pharm Bull , vol.47 , pp. 454-455
    • Fukuyama, Y.1    Yokoyama, R.2    Ohsaki, A.3    Takahashi, H.4    Minami, H.5
  • 26
    • 36949063857 scopus 로고
    • Determination of the absolute configuration of optically active compounds by means of X-rays
    • Bijvoet JM, Peerdeman AF, Van Bammel AJ. Determination of the absolute configuration of optically active compounds by means of X-rays. Nature 1951; 168: 271-2
    • (1951) Nature , vol.168 , pp. 271-272
    • Bijvoet, J.M.1    Peerdeman, A.F.2    Van Bammel, A.J.3
  • 27
    • 0001153409 scopus 로고
    • The indexing of reflexions in investigations involving the use of the anomalous scattering effect
    • Peerdeman AF, Bijvoet JM. The indexing of reflexions in investigations involving the use of the anomalous scattering effect. Acta Crystallogr 1956; 9: 1012-5
    • (1956) Acta Crystallogr , vol.9 , pp. 1012-1015
    • Peerdeman, A.F.1    Bijvoet, J.M.2
  • 29
    • 33947206554 scopus 로고    scopus 로고
    • Utility of a chiral 1,3-dioxane template in stereoselective intramolecular Diels-Alder reactions
    • Evanno L, Deville A, Dubost L, Chiaroni A, Bodo B, Nay B. Utility of a chiral 1,3-dioxane template in stereoselective intramolecular Diels-Alder reactions. Tetrahedron Lett 2007; 48: 2893 - 6
    • (2007) Tetrahedron Lett , vol.48 , pp. 2893-2896
    • Evanno, L.1    Deville, A.2    Dubost, L.3    Chiaroni, A.4    Bodo, B.5    Nay, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.