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Volumn 80, Issue 11, 2014, Pages 861-869

Erythroidine alkaloids: A novel class of phytoestrogens

Author keywords

alkaloids; Erythrina poeppigiana; erythroidines; Fabaceae; phytoestrogens; reporter gene assay

Indexed keywords

8 OXO ALPHA ERYTHROIDINE; 8 OXO BETA ERYTHROIDINE; ALKALOID DERIVATIVE; ALPHA ERYTHROIDINE; BETA ERYTHROIDINE; ESTRADIOL; ESTROGEN RECEPTOR ALPHA; ESTROGEN RECEPTOR BETA; METHANOL; PHYTOESTROGEN; UNCLASSIFIED DRUG; ALKALOID; BETA-ERYTHROIDINE; DIHYDRO BETA ERYTHROIDINE; ESTROGEN RECEPTOR ALPHA, HUMAN; PLANT EXTRACT; RECOMBINANT PROTEIN;

EID: 84905995166     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0034-1382861     Document Type: Article
Times cited : (27)

References (35)
  • 1
    • 34147115385 scopus 로고    scopus 로고
    • Ethnobotany of the Samburu of Mt. Nyiru, South Turkana, Kenya
    • Bussmann R. W. Ethnobotany of the Samburu of Mt. Nyiru, South Turkana, Kenya. J Ethnobiol Ethnomed: 2006; 2 35
    • (2006) J Ethnobiol Ethnomed , vol.2 , pp. 35
    • Bussmann, R.W.1
  • 3
    • 84855544913 scopus 로고    scopus 로고
    • In vitro estrogenic activity of two major compounds from the stem bark of Erythrina lysistemon (Fabaceae)
    • Magne Ndé C., Njamen D., Tanee Fomum S., Wandji J., Simpson E., Clyne C., Vollmer G. In vitro estrogenic activity of two major compounds from the stem bark of Erythrina lysistemon (Fabaceae). Eur J Pharmacol: 2012; 674 87 94
    • (2012) Eur J Pharmacol , vol.674 , pp. 87-94
    • Magne Ndé, C.1    Njamen, D.2    Tanee Fomum, S.3    Wandji, J.4    Simpson, E.5    Clyne, C.6    Vollmer, G.7
  • 4
    • 80054705824 scopus 로고    scopus 로고
    • Assessing sub-Saharan Erythrina for efficacy: Traditional uses, biological activities and phytochemistry
    • Kone W. M., Solange K. N., Dosso M. Assessing sub-Saharan Erythrina for efficacy: traditional uses, biological activities and phytochemistry. Pak J Biol Sci: 2011; 14 560 571
    • (2011) Pak J Biol Sci , vol.14 , pp. 560-571
    • Kone, W.M.1    Solange, K.N.2    Dosso, M.3
  • 5
    • 33845944472 scopus 로고    scopus 로고
    • Herbal care for reproductive health: Ethno medicobotany from Uttara Kannada district in Karnataka, India
    • Hegde H. V., Hegde G. R., Kholkute S. D. Herbal care for reproductive health: ethno medicobotany from Uttara Kannada district in Karnataka, India. Complement Ther Clin Pract: 2007; 13 38 45
    • (2007) Complement Ther Clin Pract , vol.13 , pp. 38-45
    • Hegde, H.V.1    Hegde, G.R.2    Kholkute, S.D.3
  • 6
    • 70349502124 scopus 로고    scopus 로고
    • Isoflavonoids from Erythrina peppigiana: Evaluation of their binding affinity for the estrogen receptor
    • Djiogue S., Halabalaki M., Alexi X., Njamen D., Fomum Z. T., Alexis M. N., Skaltsounis A. L. Isoflavonoids from Erythrina peppigiana: evaluation of their binding affinity for the estrogen receptor. J Nat Prod: 2009; 72 1603 1607
    • (2009) J Nat Prod , vol.72 , pp. 1603-1607
    • Djiogue, S.1    Halabalaki, M.2    Alexi, X.3    Njamen, D.4    Fomum, Z.T.5    Alexis, M.N.6    Skaltsounis, A.L.7
  • 8
    • 0141829776 scopus 로고    scopus 로고
    • Phytoestrogens: A review of the present state of research
    • DOI 10.1002/ptr.1364
    • Ososki A. L., Kennelly E. J. Phytoestrogens: a review of the present state of research. Phytother Res: 2003; 17 845 869 (Pubitemid 37157993)
    • (2003) Phytotherapy Research , vol.17 , Issue.8 , pp. 845-869
    • Ososki, A.L.1    Kennelly, E.J.2
  • 9
    • 0028003678 scopus 로고
    • Mixed estrogenic and anti-estrogenic activities of yuehchukene - a bis-indole alkaloid
    • DOI 10.1016/0014-2999(94)90628-9
    • Ng P. C., Ho D. D., Ng K. H., Kong Y. C., Cheng K. F., Stone G. Mixed estrogenic and anti-estrogenic activities of yuechukene - a bis -indole alkaloid. Eur J Pharmacol: 1994; 264 1 12 (Pubitemid 24310826)
    • (1994) European Journal of Pharmacology , vol.264 , Issue.1 , pp. 1-12
    • Ng, P.C.1    Ho, D.D.2    Ng, K.H.3    Kong, Y.C.4    Cheng, K.F.5    Stone, G.6
  • 10
    • 0035498215 scopus 로고    scopus 로고
    • Estrogenic activity as a function of chemical structure in Haplophyllum quinoline alkaloids
    • Nazrullaev S. S., Bessonova I. A., Akhmedkhodzaeva K. HS. Estrogenic activity as a function of chemical structure in Haplophyllum quinoline alkaloids. Chem Nat Compd: 2001; 37 551 555
    • (2001) Chem Nat Compd , vol.37 , pp. 551-555
    • Nazrullaev, S.S.1    Bessonova, I.A.2    Akhmedkhodzaeva, K.H.3
  • 11
    • 70349308395 scopus 로고    scopus 로고
    • Trigonelline is a novel phytoestrogen in coffee beans
    • Allred K. F., Yackley K. M., Vanamala J., Allred C. D. Trigonelline is a novel phytoestrogen in coffee beans. J Nutr: 2009; 139 1833 1838
    • (2009) J Nutr , vol.139 , pp. 1833-1838
    • Allred, K.F.1    Yackley, K.M.2    Vanamala, J.3    Allred, C.D.4
  • 12
    • 0000618128 scopus 로고
    • Alkaloids from the flowers of Erythrina americana
    • Aguilar M. I., Giral F., Espejo O. Alkaloids from the flowers of Erythrina americana. Phytochemistry: 1981; 20 2061 2062
    • (1981) Phytochemistry , vol.20 , pp. 2061-2062
    • Aguilar, M.I.1    Giral, F.2    Espejo, O.3
  • 13
    • 0008937917 scopus 로고
    • Alkaloids in seeds of four Erythrina species
    • Chawla A. S., Redha F. M., Jackson A. H. Alkaloids in seeds of four Erythrina species. Phytochemistry: 1985; 24 1821 1823
    • (1985) Phytochemistry , vol.24 , pp. 1821-1823
    • Chawla, A.S.1    Redha, F.M.2    Jackson, A.H.3
  • 15
    • 35048834712 scopus 로고    scopus 로고
    • Subtype-specific activation of estrogen receptors by a special extract of Rheum rhaponticum (ERr 731®), its aglycones and structurally related compounds in U2OS human osteosarcoma cells
    • DOI 10.1016/j.phymed.2007.09.001, PII S0944711307002164
    • Möller F., Zierau O., Jandausch A., Rettenberger R., Kaszkin-Bettag M., Vollmer G. Subtype-specific activation of estrogen receptors by a special extract of Rheum rhaponticum (ERr 731R), its aglycones and structurally related compounds in U2OS human osteosarcoma cells. Phytomedicine: 2007; 14 716 726 (Pubitemid 47554506)
    • (2007) Phytomedicine , vol.14 , Issue.11 , pp. 716-726
    • Moller, F.1    Zierau, O.2    Jandausch, A.3    Rettenberger, R.4    Kaszkin-Bettag, M.5    Vollmer, G.6
  • 17
    • 84905979241 scopus 로고    scopus 로고
    • Herz W. Falk H. Kirby G.W. eds. Progress in the chemistry of organic natural products Wien, New York Springer
    • Reimann E. Synthesis pathways to Erythrina alkaloids and Erythrina type compounds. In: Herz W., Falk H., Kirby G. W. eds. Progress in the chemistry of organic natural products. Wien, New York Springer: 2007; 1 56
    • (2007) Synthesis Pathways to Erythrina Alkaloids and Erythrina Type Compounds , pp. 1-56
    • Reimann, E.1
  • 18
    • 25044453860 scopus 로고
    • The crystal structure of dihydro-β-erythroidine hydrobromide
    • Hanson A. W. The crystal structure of dihydro- β -erythroidine hydrobromide. Acta Cryst: 1963; 16 939 942
    • (1963) Acta Cryst , vol.16 , pp. 939-942
    • Hanson, A.W.1
  • 20
    • 0035935731 scopus 로고    scopus 로고
    • Estrogen receptor-β potency-selective ligands: Structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues
    • DOI 10.1021/jm010254a
    • Meyers M. J., Sun J., Carlson K. E., Marriner G. A., Katzenellenbogen B. S., Katzenellenbogen J. A. Estrogen receptor-beta potency-selective ligands: structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues. J Med Chem: 2001; 44 4230 4251 (Pubitemid 33095330)
    • (2001) Journal of Medicinal Chemistry , vol.44 , Issue.24 , pp. 4230-4251
    • Meyers, M.J.1    Sun, J.2    Carlson, K.E.3    Marriner, G.A.4    Katzenellenbogen, B.S.5    Katzenellenbogen, J.A.6
  • 22
  • 25
    • 78650877960 scopus 로고    scopus 로고
    • SGK3 is an estrogen-inducible kinase promoting estrogen-mediated survival of breast cancer cells
    • Wang Y., Zhou D., Phung S., Masri S., Smith D., Chen S. SGK3 is an estrogen-inducible kinase promoting estrogen-mediated survival of breast cancer cells. Mol Endocrinol: 2011; 25 72 82
    • (2011) Mol Endocrinol , vol.25 , pp. 72-82
    • Wang, Y.1    Zhou, D.2    Phung, S.3    Masri, S.4    Smith, D.5    Chen, S.6
  • 26
    • 84891601821 scopus 로고    scopus 로고
    • In vivo and in vitro estrogenic activity of extracts from Erythrina poeppigiana (Fabaceae)
    • Njamen D., Djiogue S., Zingue S., Mvondo M. A., Nkeh-Chungag B. In vivo and in vitro estrogenic activity of extracts from Erythrina poeppigiana (Fabaceae). J Complement Integr Med: 2013; 10 1 11
    • (2013) J Complement Integr Med , vol.10 , pp. 1-11
    • Njamen, D.1    Djiogue, S.2    Zingue, S.3    Mvondo, M.A.4    Nkeh-Chungag, B.5
  • 28
    • 0037665217 scopus 로고    scopus 로고
    • An arylbenzofuran and four isoflavonoids from the roots of Erythrina poeppigiana
    • DOI 10.1016/S0031-9422(03)00184-5
    • Tanaka H., Oh-Uchi T., Etoh H., Sako M., Sato M., Fukai T., Tateishi Y. An arylbenzofuran and four isoflavonoids from the roots of Erythrina poeppigiana. Phytochemistry: 2003; 63 597 602 (Pubitemid 36736301)
    • (2003) Phytochemistry , vol.63 , Issue.5 , pp. 597-602
    • Tanaka, H.1    Oh-Uchi, T.2    Etoh, H.3    Sako, M.4    Sato, M.5    Fukai, T.6    Tateishi, Y.7
  • 29
    • 37049123961 scopus 로고
    • Phenol oxidation and biosynthesis. Part XXII the alkaloids of Erythrina lysistemon, E abyssinica, E poeppigiana, E fusca, and E lithosperma; The structure of erythratidine
    • Barton D. HR, Gunatilaka A. L., Letcher R. M., Lobo A. MF, Widdowson D. A. Phenol oxidation and biosynthesis. Part XXII. The alkaloids of Erythrina lysistemon, E. abyssinica, E. poeppigiana, E. fusca, and E. lithosperma; the structure of erythratidine. Chem Soc Perkin Trans I: 1973; 1 874 880
    • (1973) Chem Soc Perkin Trans i , vol.1 , pp. 874-880
    • Barton, D.H.1    Gunatilaka, A.L.2    Letcher, R.M.3    Lobo, A.M.4    Widdowson, D.A.5
  • 30
    • 0035671974 scopus 로고    scopus 로고
    • Erythrinan alkaloids and isoflavonoids from Erythrina poeppigiana
    • DOI 10.1055/s-2001-18852
    • Tanaka H., Etoh H., Shimizu H., Oh-Uchi T., Terada Y., Tateishi Y. Erythrinan alkaloids and isoflavonoids from Erythrina poeppigiana. Planta Med: 2001; 67 871 873 (Pubitemid 34015556)
    • (2001) Planta Medica , vol.67 , Issue.9 , pp. 871-873
    • Tanaka, H.1    Etoh, H.2    Shimizu, H.3    Oh-Uchi, T.4    Terada, Y.5    Tateishi, Y.6
  • 32
    • 3242798960 scopus 로고    scopus 로고
    • Phytoestrogens and their human metabolites show distinct agonistic and antagonistic properties on estrogen receptor α (ERα) and ERβ in human cells
    • DOI 10.1093/toxsci/kfh147
    • Mueller S. O., Simon S., Chae K., Metzler M., Korach K. S. Phytoestrogens and their human metabolites show distinct agonistic and antagonistic properties on estrogen receptor alpha (ERalpha) and ERbeta in human cells. Toxicol Sci: 2004; 80 14 25 (Pubitemid 38967392)
    • (2004) Toxicological Sciences , vol.80 , Issue.1 , pp. 14-25
    • Mueller, S.O.1    Simon, S.2    Chae, K.3    Metzler, M.4    Korach, K.S.5
  • 33
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods: 1983; 65 55 63 (Pubitemid 14203433)
    • (1983) Journal of Immunological Methods , vol.65 , Issue.1-2 , pp. 55-63
    • Mosmann, T.1
  • 35
    • 0033562350 scopus 로고    scopus 로고
    • Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro
    • DOI 10.1006/abio.1999.4085
    • Winer J., Jung C. K., Shackel I., Williams P. M. Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro. Anal Biochem: 1999; 270 41 49 (Pubitemid 29230718)
    • (1999) Analytical Biochemistry , vol.270 , Issue.1 , pp. 41-49
    • Winer, J.1    Jung, C.K.S.2    Shackel, I.3    Williams, P.M.4


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