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Volumn 27, Issue 1, 2004, Pages 35-39

Distribution of (-)-yatein in cupressaceae family analysed by high performance liquid chromatography

Author keywords

Chiral separation; Cupressaceae family; HPLC; Yatein

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; DRUG DERIVATIVE; GAMMA BUTYROLACTONE; YATEIN;

EID: 6944236340     PISSN: 02536269     EISSN: 02536269     Source Type: Journal    
DOI: 10.1007/BF02980042     Document Type: Article
Times cited : (8)

References (23)
  • 1
    • 0030248506 scopus 로고    scopus 로고
    • Antitumour-promoting and antitumour activities of the crude extract from the leaves of Juniperus chinensis
    • Ali, A. M., Mackeen, M. M., Intan-Safinar, I., Hamid, M., Lajis., N. H., and Sharkoshi, S. H. E., Antitumour-promoting and antitumour activities of the crude extract from the leaves of Juniperus chinensis. J. Ethnopharmacol., 53, 165-169 (1996).
    • (1996) J. Ethnopharmacol. , vol.53 , pp. 165-169
    • Ali, A.M.1    Mackeen, M.M.2    Intan-Safinar, I.3    Hamid, M.4    Lajis, N.H.5    Sharkoshi, S.H.E.6
  • 2
    • 0035070986 scopus 로고    scopus 로고
    • The antioxidant activity of the essential oils of Artemisia afra, Artemisia abyssinica and Juniperus procera
    • Burits, M., Asres, K., and Bucar, F., The antioxidant activity of the essential oils of Artemisia afra, Artemisia abyssinica and Juniperus procera. Phytother. Res., 15, 103-108 (2001).
    • (2001) Phytother. Res. , vol.15 , pp. 103-108
    • Burits, M.1    Asres, K.2    Bucar, F.3
  • 3
    • 0019126209 scopus 로고
    • Plant anticancer agents. X. Lignans from Juniperus phoenicea
    • Cairnes, D. A., Ekundayo, O., and Kingston, D. G., Plant anticancer agents. X. Lignans from Juniperus phoenicea. J. Nat. Prod., 43, 495-497 (1980).
    • (1980) J. Nat. Prod. , vol.43 , pp. 495-497
    • Cairnes, D.A.1    Ekundayo, O.2    Kingston, D.G.3
  • 4
    • 0019513231 scopus 로고
    • High performance liquid chromatography of podophyllotoxines and related lignans
    • Cairnes, D. A., Kingston, D. G. I., and Rao, M. M., High performance liquid chromatography of podophyllotoxines and related lignans. J. Nat. Prod., 44, 34-37 (1981).
    • (1981) J. Nat. Prod. , vol.44 , pp. 34-37
    • Cairnes, D.A.1    Kingston, D.G.I.2    Rao, M.M.3
  • 6
    • 0344563459 scopus 로고    scopus 로고
    • Antimicrobial activities of several parts of Pinus brutia, Juniperus oxycedrus, Abies cilicia, Cedrus libani and Pinus nigra
    • Digrak, M., Ilcim, A., and Hakki, A. M., Antimicrobial activities of several parts of Pinus brutia, Juniperus oxycedrus, Abies cilicia, Cedrus libani and Pinus nigra. Phytother. Res., 13 , 584-587 (1999).
    • (1999) Phytother. Res. , vol.13 , pp. 584-587
    • Digrak, M.1    Ilcim, A.2    Hakki, A.M.3
  • 8
    • 37049086526 scopus 로고
    • Chiral synthesis of lignan lactones, (-)-hinokinin, (-)-deoxypodorhizone, (-)-isohibalactone and (-)-savinin by means of enantioselective deprotonation strategy
    • Honda, T., Kimura, N., Sato, S., Kato, D., and Tominaga, H., Chiral synthesis of lignan lactones, (-)-hinokinin, (-)-deoxypodorhizone, (-)-isohibalactone and (-)-savinin by means of enantioselective deprotonation strategy. J. Chem. Soc. Perkin Trans., 1, 1043-1046 (1994).
    • (1994) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1043-1046
    • Honda, T.1    Kimura, N.2    Sato, S.3    Kato, D.4    Tominaga, H.5
  • 9
    • 0033057154 scopus 로고    scopus 로고
    • Identification of Thuja occidentalis lignans and its biosynthetic relationship
    • Kawai, S., Sugishita, K., and Ohashi, H., Identification of Thuja occidentalis lignans and its biosynthetic relationship. Phytochem., 51, 243-247 (1999).
    • (1999) Phytochem. , vol.51 , pp. 243-247
    • Kawai, S.1    Sugishita, K.2    Ohashi, H.3
  • 10
    • 0036594845 scopus 로고    scopus 로고
    • 2,3-Dibenzylbutyrolactones and 1,2,3,4-tetrahydro-2-naphthoic acid gamma-lactones: Structure and activity relationship in cytotoxic activity
    • Kim, Y., You, Y. J., Nam, N. H., and Ahn, B. Z., 2,3- Dibenzylbutyrolactones and 1,2,3,4-tetrahydro-2-naphthoic acid gamma-lactones: structure and activity relationship in cytotoxic activity. Arch. Pharm. Res., 25, 240-249 (2002).
    • (2002) Arch. Pharm. Res. , vol.25 , pp. 240-249
    • Kim, Y.1    You, Y.J.2    Nam, N.H.3    Ahn, B.Z.4
  • 11
    • 0035671972 scopus 로고    scopus 로고
    • A fast and simple GC-MS method for lignan profiling in Anthriscus sylvestris and biosynthetically related plant species
    • Koulman, A., Bos, R., Medarde, M., Pras, N., and Quax, W. J., A fast and simple GC-MS method for lignan profiling in Anthriscus sylvestris and biosynthetically related plant species. Planta Med., 67, 858-862 (2001).
    • (2001) Planta Med. , vol.67 , pp. 858-862
    • Koulman, A.1    Bos, R.2    Medarde, M.3    Pras, N.4    Quax, W.J.5
  • 12
    • 0035022905 scopus 로고    scopus 로고
    • Diterpenoids from the leaves of Juniperus chinensis var. kaizuka
    • Lee, C. K. and Cheng, Y. S., Diterpenoids from the leaves of Juniperus chinensis var. kaizuka. J. Nat. Prod., 64, 511-514 (2001).
    • (2001) J. Nat. Prod. , vol.64 , pp. 511-514
    • Lee, C.K.1    Cheng, Y.S.2
  • 14
    • 0036919011 scopus 로고    scopus 로고
    • Stereoselective determination of (-)-yatein in the plant of the Cupressaceae family by capillary electrophoresis
    • Lim, H. M., Kim, Y., Kim, Y. H., Ahn, B. Z., and Kang, J. S., Stereoselective determination of (-)-yatein in the plant of the Cupressaceae family by capillary electrophoresis. J. Sep. Sci., 25, 1070-1072 (2002).
    • (2002) J. Sep. Sci. , vol.25 , pp. 1070-1072
    • Lim, H.M.1    Kim, Y.2    Kim, Y.H.3    Ahn, B.Z.4    Kang, J.S.5
  • 15
    • 0015458783 scopus 로고
    • Antitumor activity of Bursera schlechtendalii (Burseraceae): Isolation and structure determination of two new lignans
    • McDoniel, P. B. and Cole. J. R., Antitumor activity of Bursera schlechtendalii (Burseraceae): Isolation and structure determination of two new lignans. J. Pharm. Sci., 61, 1992-1994 (1972).
    • (1972) J. Pharm. Sci. , vol.61 , pp. 1992-1994
    • McDoniel, P.B.1    Cole, J.R.2
  • 16
    • 0028840759 scopus 로고
    • Synthesis, antitumoral and antiviral evaluation of halo- And demethyl-yatein derivatives
    • Medarde, M., Clairac, R. P., Lopez, J. L., Gravalos, D. G., and San Feliciano, A., Synthesis, antitumoral and antiviral evaluation of halo- and demethyl-yatein derivatives. Arch. Pharm., 328, 640-644 (1995).
    • (1995) Arch. Pharm. , vol.328 , pp. 640-644
    • Medarde, M.1    Clairac, R.P.2    Lopez, J.L.3    Gravalos, D.G.4    San Feliciano, A.5
  • 17
    • 0346315935 scopus 로고    scopus 로고
    • Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J. chinensis
    • Miyata, M., Itoh, K., and Tachibana, S., Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J. chinensis. J. Wood Sci., 44, 397-400 (1998).
    • (1998) J. Wood Sci. , vol.44 , pp. 397-400
    • Miyata, M.1    Itoh, K.2    Tachibana, S.3
  • 19
    • 0027941393 scopus 로고
    • Synthesis of stereospecifically deuterated matairesinol, podorhizol, epipodorhizol, and yatein
    • Neidigh, K. A., Kingston, D., Lewis, G. I., and Norman, G., Synthesis of stereospecifically deuterated matairesinol, podorhizol, epipodorhizol, and yatein. J. Nat. Prod., 57, 791-800 (1994).
    • (1994) J. Nat. Prod. , vol.57 , pp. 791-800
    • Neidigh, K.A.1    Kingston, D.2    Lewis, G.I.3    Norman, G.4
  • 22
    • 0028364477 scopus 로고
    • Antiplatelet and vasorelaxing actions of the acetoxy derivative of cedranediol isolated from Juniperus squamata
    • Teng, C. M., Lin, C. H., Kuo, Y. H., Lin, Y. L., and Huang, T. F., Antiplatelet and vasorelaxing actions of the acetoxy derivative of cedranediol isolated from Juniperus squamata. Planta Med., 60, 209-213 (1994).
    • (1994) Planta Med. , vol.60 , pp. 209-213
    • Teng, C.M.1    Lin, C.H.2    Kuo, Y.H.3    Lin, Y.L.4    Huang, T.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.