메뉴 건너뛰기




Volumn 148, Issue 2, 1999, Pages 111-119

Immunoanalysis of isoflavonoids in Pisum sativum and Vigna radiata

Author keywords

7 methoxy isoflavonoid; Immunoassay; Isoflavonoid; Isoformononetin; Pisum sativum; Prunetin; Vigna radiata

Indexed keywords

ALCOHOL; BIOCHANIN A; DAIDZEIN; FORMONONETIN; GENISTEIN; GENISTIN; GLUCOSIDE; ISOFLAVONOID; PRUNETIN; SILICON DERIVATIVE; SILICON DIOXIDE;

EID: 0344563479     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9452(99)00125-9     Document Type: Article
Times cited : (35)

References (31)
  • 1
    • 0030198725 scopus 로고    scopus 로고
    • Diverse functions of isoflavonoids in legumes transcend anti-microbial definitions of phytoalexins
    • Dakora F.D., Phillips D.A. Diverse functions of isoflavonoids in legumes transcend anti-microbial definitions of phytoalexins. Physiol. Mol. Plant Pathol. 49:1996;1-20.
    • (1996) Physiol. Mol. Plant Pathol. , vol.49 , pp. 1-20
    • Dakora, F.D.1    Phillips, D.A.2
  • 2
    • 0003096846 scopus 로고
    • The Isoflavonoids
    • T.A. Geissman. Oxford: Pergamon Press LTD
    • Ollis W.D. The Isoflavonoids. Geissman T.A. The Chemistry of Flavonoid Compounds. 1962;353-399 Pergamon Press LTD, Oxford.
    • (1962) The Chemistry of Flavonoid Compounds , pp. 353-399
    • Ollis, W.D.1
  • 4
    • 0030047573 scopus 로고    scopus 로고
    • Isotope dilution gas chromatographic-mass spectrometric method for the determination of isoflavonoids, coumestrol, and lignans in food samples
    • Mazur W., Fotsis T., Wähälä K.T., Ojala S., Salakka A., Adlercreutz H. Isotope dilution gas chromatographic-mass spectrometric method for the determination of isoflavonoids, coumestrol, and lignans in food samples. Anal. Biochem. 233:1996;169-180.
    • (1996) Anal. Biochem. , vol.233 , pp. 169-180
    • Mazur, W.1    Fotsis, T.2    Wähälä, K.T.3    Ojala, S.4    Salakka, A.5    Adlercreutz, H.6
  • 5
    • 0030976331 scopus 로고    scopus 로고
    • Phytoestrogens and western diseases
    • Adlercreutz H., Mazur W. Phytoestrogens and western diseases. Annals Med. 29:1997;95-120.
    • (1997) Annals Med. , vol.29 , pp. 95-120
    • Adlercreutz, H.1    Mazur, W.2
  • 11
    • 0345602403 scopus 로고
    • Synthesis of corylin methyl ether - Structures of corylin & neobavaisoflavone
    • Jain A.C., Singh J. Synthesis of corylin methyl ether - structures of corylin & neobavaisoflavone. Indian J. Chem. 13:1975;789-790.
    • (1975) Indian J. Chem. , vol.13 , pp. 789-790
    • Jain, A.C.1    Singh, J.2
  • 12
    • 0027194818 scopus 로고
    • Studies on zoospore attracting activity. II. Synthesis of isoflavones and their attracting activity to Aphanomyces enteiches zoospore
    • Sekizaki H., Yokosawa R., Chinen Ch., Adachi H., Yamane Y. Studies on zoospore attracting activity. II. Synthesis of isoflavones and their attracting activity to Aphanomyces enteiches zoospore. Biol. Pharm. Bull. 16:1993;698-701.
    • (1993) Biol. Pharm. Bull. , vol.16 , pp. 698-701
    • Sekizaki, H.1    Yokosawa, R.2    Chinen, Ch.3    Adachi, H.4    Yamane, Y.5
  • 14
    • 0031938158 scopus 로고    scopus 로고
    • The measurement of the isoflavone daidzein by time resolved fluorescence immunoassay: A method for assessment of dietary soya exposure
    • Kohen F., Lichter S., Gayer B., DeBoever J., Lu L.J.W. The measurement of the isoflavone daidzein by time resolved fluorescence immunoassay: a method for assessment of dietary soya exposure. J. Steroid Biochem. Molec. Biol. 64:1998;217-222.
    • (1998) J. Steroid Biochem. Molec. Biol. , vol.64 , pp. 217-222
    • Kohen, F.1    Lichter, S.2    Gayer, B.3    Deboever, J.4    Lu, L.J.W.5
  • 17
    • 0000968496 scopus 로고
    • Isoflavone O-methyltransferase activities in elicitor treated cell suspension cultures of medicago sativa
    • Edwards R., Dixon R. Isoflavone O-methyltransferase activities in elicitor treated cell suspension cultures of medicago sativa. Phytochemistry. 30:1991;2597-2606.
    • (1991) Phytochemistry , vol.30 , pp. 2597-2606
    • Edwards, R.1    Dixon, R.2
  • 18
    • 0344307879 scopus 로고
    • The chemistry of extractives from hardwoods. Part VIII.* The isolation of 5:4′-dihydroxy-7-methoxyisoflavone (Prunetin) from the heartwood of Pterocarpus angolensis and a synthesis of 7:4′-dihydroxy-5-methoxyisoflavone hitherto known as prunusetin
    • F.E. King, L. Jurd, The chemistry of extractives from hardwoods. Part VIII.* The isolation of 5:4′-dihydroxy-7-methoxyisoflavone (Prunetin) from the heartwood of Pterocarpus angolensis and a synthesis of 7:4′-dihydroxy-5-methoxyisoflavone hitherto known as prunusetin, J. Chem. Soc. (1952) 3211-3215.
    • (1952) J. Chem. Soc. , pp. 3211-3215
    • King, F.E.1    Jurd, L.2
  • 19
    • 0345170338 scopus 로고
    • Composés flavoniques des extraits de bois. VI.-Sur les composés flavoniques du bois de Prunus mahaleb
    • Pacheco H. Composés flavoniques des extraits de bois. VI.-Sur les composés flavoniques du bois de Prunus mahaleb. Bull. Soc. Chim. Biol. 41:1959;111-117.
    • (1959) Bull. Soc. Chim. Biol. , vol.41 , pp. 111-117
    • Pacheco, H.1
  • 24
    • 0001382913 scopus 로고
    • Structures of prenylated dihydrochalcone, Gancaonin J and homoisoflavanone, Gancaonin K from Glycyrrhiza pallidiflora
    • Fukai T., Wang Q., Inami R., Nomura T. Structures of prenylated dihydrochalcone, Gancaonin J and homoisoflavanone, Gancaonin K from Glycyrrhiza pallidiflora. Heterocycles. 31:1990;643-650.
    • (1990) Heterocycles , vol.31 , pp. 643-650
    • Fukai, T.1    Wang, Q.2    Inami, R.3    Nomura, T.4
  • 25
    • 0000090995 scopus 로고
    • Flavonoid 5-glucosides from Prunus cerasus bark and their characteristic weak glycosidic bonding
    • Geibel M., Feucht W. Flavonoid 5-glucosides from Prunus cerasus bark and their characteristic weak glycosidic bonding. Phytochemistry. 30:1991;1519-1522.
    • (1991) Phytochemistry , vol.30 , pp. 1519-1522
    • Geibel, M.1    Feucht, W.2
  • 26
    • 0026354323 scopus 로고
    • Three new flavonoids, 3′-methoxylupin, laxifolin, and isolaxifolin from the roots of Derris laxiflora Benth
    • Lin Y.L., Chen Y.L., Kuo Y.H. Three new flavonoids, 3′-methoxylupin, laxifolin, and isolaxifolin from the roots of Derris laxiflora Benth. Chem. Pharm. Bull. 39:1991;3132-3135.
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 3132-3135
    • Lin, Y.L.1    Chen, Y.L.2    Kuo, Y.H.3
  • 28
    • 0030458697 scopus 로고    scopus 로고
    • Affinity chromatography, substrate/product specificity and amino acid sequence analysis of an isoflavone O-methyl transferase from alfalfa (Medicago sativa L.)
    • He X.Z., Dixon R.A. Affinity chromatography, substrate/product specificity and amino acid sequence analysis of an isoflavone O-methyl transferase from alfalfa (Medicago sativa L.). Arch. Biochem. Biophys. 336:1996;121-129.
    • (1996) Arch. Biochem. Biophys. , vol.336 , pp. 121-129
    • He, X.Z.1    Dixon, R.A.2
  • 29
    • 0031881338 scopus 로고    scopus 로고
    • Stress response in alfalfa (Medicago sativa L.). XXII. CDNA cloning and characterization of an elicitor inducible isoflavone 7-O-methyltransferase
    • He X.Z., Reddy J.T., Dixon R.A. Stress response in alfalfa (Medicago sativa L.). XXII. CDNA cloning and characterization of an elicitor inducible isoflavone 7-O-methyltransferase. Plant. Mol. Biol. 36:1998;43-54.
    • (1998) Plant. Mol. Biol. , vol.36 , pp. 43-54
    • He, X.Z.1    Reddy, J.T.2    Dixon, R.A.3
  • 30
    • 0000731153 scopus 로고
    • Biosynthesis, elicitation and biological activity of isoflavonoid phytoalexins
    • Smith D.A., Banks S.W. Biosynthesis, elicitation and biological activity of isoflavonoid phytoalexins. Phytochemistry. 25:1986;979-995.
    • (1986) Phytochemistry , vol.25 , pp. 979-995
    • Smith, D.A.1    Banks, S.W.2
  • 31
    • 0011290810 scopus 로고
    • A O-hydroxychalcone and flavonoids from alfalfa callus stimulated by a fungal naftochinone
    • Kobayashi A., Yata S, Kawazu K. A O-hydroxychalcone and flavonoids from alfalfa callus stimulated by a fungal naftochinone. Agric. Biol. Chem. 52:1988;3223-3227.
    • (1988) Agric. Biol. Chem. , vol.52 , pp. 3223-3227
    • Kobayashi, A.1    Yata, S.2    Kawazu, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.