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Volumn 40, Issue 11, 2005, Pages 1081-1105

Astonishing diversity of natural surfactants: 6. Biologically active marine and terrestrial alkaloid glycosides

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTICS; ANTIOXIDANTS; MARINE APPLICATIONS; MICROORGANISMS;

EID: 29444443621     PISSN: 00244201     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11745-005-1473-2     Document Type: Review
Times cited : (39)

References (230)
  • 1
    • 27444447348 scopus 로고    scopus 로고
    • Astonishing diversity of natural surfactants. 5. Biological active glycosides of aromatic metabolites
    • Dembitsky, V.M. (2005) Astonishing Diversity of Natural Surfactants. 5. Biological Active Glycosides of Aromatic Metabolites, Lipids 40, 869-900.
    • (2005) Lipids , vol.40 , pp. 869-900
    • Dembitsky, V.M.1
  • 8
    • 4344714713 scopus 로고    scopus 로고
    • Marine toxins and nonmarine toxins: Convergence or symbiotic organisms?
    • Daly, J.W. (2004) Marine Toxins and Nonmarine Toxins: Convergence or Symbiotic Organisms? J. Nat. Prod. 67, 1211-1215.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1211-1215
    • Daly, J.W.1
  • 9
    • 0031931850 scopus 로고    scopus 로고
    • Thirty years of discovering arthropod alkaloids in amphibian skin
    • Daly, J.W. (1998) Thirty Years of Discovering Arthropod Alkaloids in Amphibian Skin, J. Nat. Prod. 61, 162-172.
    • (1998) J. Nat. Prod. , vol.61 , pp. 162-172
    • Daly, J.W.1
  • 10
    • 19044394540 scopus 로고    scopus 로고
    • Bioactive natural products from marine invertebrates and associated fungi
    • Proksch, P., Ebel, R., Edrada, R.A., Wray, V., and Steube, K. (2003) Bioactive Natural Products from Marine Invertebrates and Associated Fungi, Prog. Mol. Subcell. Biol. 37, 117-142.
    • (2003) Prog. Mol. Subcell. Biol. , vol.37 , pp. 117-142
    • Proksch, P.1    Ebel, R.2    Edrada, R.A.3    Wray, V.4    Steube, K.5
  • 11
    • 14744287300 scopus 로고    scopus 로고
    • Novel antitumor agents: Marine sponge alkaloids, their synthetic analogs and derivatives
    • Dembitsky, V.M., Gloriozova, T.A., and Poroikov, V.V. (2005) Novel Antitumor Agents: Marine Sponge Alkaloids, Their Synthetic Analogs and Derivatives, Mini Rev. Med. Chem. 5, 319-336.
    • (2005) Mini Rev. Med. Chem. , vol.5 , pp. 319-336
    • Dembitsky, V.M.1    Gloriozova, T.A.2    Poroikov, V.V.3
  • 12
    • 0036087069 scopus 로고    scopus 로고
    • Cytotoxic anticancer candidates from natural resources
    • Kim, J., and Park, E.J. (2002) Cytotoxic Anticancer Candidates from Natural Resources, Curr. Med. Chem. Anti-Cancer Agents 2, 485-537.
    • (2002) Curr. Med. Chem. Anti-Cancer Agents , vol.2 , pp. 485-537
    • Kim, J.1    Park, E.J.2
  • 13
    • 19944410508 scopus 로고    scopus 로고
    • Solid-state fermentation systems. An overview
    • Krishna, C. (2005) Solid-State Fermentation Systems. An Overview, Crit. Rev. Biotechnol. 25, 1-30.
    • (2005) Crit. Rev. Biotechnol. , vol.25 , pp. 1-30
    • Krishna, C.1
  • 14
    • 0038742851 scopus 로고    scopus 로고
    • New genes in alkaloid metabolism and transport
    • Hashimoto, T., and Yamada, Y. (2003) New Genes in Alkaloid Metabolism and Transport, Curr. Opin. Biotechnol. 14, 163-168.
    • (2003) Curr. Opin. Biotechnol. , vol.14 , pp. 163-168
    • Hashimoto, T.1    Yamada, Y.2
  • 15
    • 0036514501 scopus 로고    scopus 로고
    • Secondary metabolites from marine microorganisms
    • Kelecom, A. (2002) Secondary Metabolites from Marine Microorganisms, An. Acad, Bras. Cienc. 74, 151-170.
    • (2002) An. Acad, Bras. Cienc. , vol.74 , pp. 151-170
    • Kelecom, A.1
  • 17
    • 0034931765 scopus 로고    scopus 로고
    • Synthesis and its application to the synthesis of biologically active natural products of new and versatile chiral building blocks
    • Toyooka, N. (2001) Synthesis and Its Application to the Synthesis of Biologically Active Natural Products of New and Versatile Chiral Building Blocks, Yakugaku Zasshi 121, 467-479.
    • (2001) Yakugaku Zasshi , vol.121 , pp. 467-479
    • Toyooka, N.1
  • 18
    • 17244373084 scopus 로고    scopus 로고
    • Development of new synthetic method using organometallic complexes and an application toward natural product synthesis
    • Mori, M. (2005) Development of New Synthetic Method Using Organometallic Complexes and an Application Toward Natural Product Synthesis, Yakugaku Zasshi 125, 51-72.
    • (2005) Yakugaku Zasshi , vol.125 , pp. 51-72
    • Mori, M.1
  • 19
    • 0037369126 scopus 로고    scopus 로고
    • Marine pyridoacridine alkaloids and synthetic analogues as antitumor agents
    • Delfourne, E., and Bastide, J. (2003) Marine Pyridoacridine Alkaloids and Synthetic Analogues as Antitumor Agents, Med. Res. Rev. 23, 234-252.
    • (2003) Med. Res. Rev. , vol.23 , pp. 234-252
    • Delfourne, E.1    Bastide, J.2
  • 20
    • 21044444206 scopus 로고    scopus 로고
    • Selective methodologies for the synthesis of biologically active piperidinic compounds
    • Cossy, J. (2005) Selective Methodologies for the Synthesis of Biologically Active Piperidinic Compounds, Chem. Rec. 5, 70-80.
    • (2005) Chem. Rec. , vol.5 , pp. 70-80
    • Cossy, J.1
  • 21
    • 35848969367 scopus 로고    scopus 로고
    • Acridone alkaloids
    • (Cordell, G.A., ed.), Academic Press, London
    • Skaltsounis, A.L., Mitaku, S., and Tillequin, F. (2000) Acridone Alkaloids, in Alkaloids (Cordell, G.A., ed.), Vol. 54, pp. 259-377, Academic Press, London.
    • (2000) Alkaloids , vol.54 , pp. 259-377
    • Skaltsounis, A.L.1    Mitaku, S.2    Tillequin, F.3
  • 22
    • 0028715581 scopus 로고
    • Antiproliferative actions of 7-substituted 1,3-dihydroxyacridones; possible involvement of DNA topoisomerase II and protein kinase C as biochemical targets
    • Bastow, K.F., Itoigawa, M., Furukawa, H., Kashiwada, Y., Bori, I.D., Ballas, L.M., and Lee, K.H. (1994) Antiproliferative Actions of 7-Substituted 1,3-Dihydroxyacridones; Possible Involvement of DNA Topoisomerase II and Protein Kinase C as Biochemical Targets, Bioorg. Med. Chem. 2, 1403-1411.
    • (1994) Bioorg. Med. Chem. , vol.2 , pp. 1403-1411
    • Bastow, K.F.1    Itoigawa, M.2    Furukawa, H.3    Kashiwada, Y.4    Bori, I.D.5    Ballas, L.M.6    Lee, K.H.7
  • 23
    • 0024489461 scopus 로고
    • In vitro and in vivo activities of atalaphillinine and related acridone alkaloids against rodent malaria
    • Fujioka, H., Nishiyama, Y., Furukawa, H., and Kumada, N. (1989) In vitro and in vivo Activities of Atalaphillinine and Related Acridone Alkaloids Against Rodent Malaria, Antimicrob. Agents Chemother. 33, 6-9.
    • (1989) Antimicrob. Agents Chemother. , vol.33 , pp. 6-9
    • Fujioka, H.1    Nishiyama, Y.2    Furukawa, H.3    Kumada, N.4
  • 24
    • 0013937331 scopus 로고
    • Alkaloids of Acronychia baueri Schott. I. Isolation of the alkaloids and a study of the antitumor and other biological properties of acronycine
    • Svoboda, G.H., Poore, G.A., Simpson, P.J., and Boder, G.B. (1966) Alkaloids of Acronychia baueri Schott. I. Isolation of the Alkaloids and a Study of the Antitumor and Other Biological Properties of Acronycine, J. Pharm. Sci. 55, 758-768.
    • (1966) J. Pharm. Sci. , vol.55 , pp. 758-768
    • Svoboda, G.H.1    Poore, G.A.2    Simpson, P.J.3    Boder, G.B.4
  • 25
    • 0015895597 scopus 로고
    • Effects of the antineoplastic alkaloid acronycine on the ultrastructure and growth patterns of cultured cells
    • Tan, P., and Auersperg, N. (1973) Effects of the Antineoplastic Alkaloid Acronycine on the Ultrastructure and Growth Patterns of Cultured Cells, Cancer Res. 33, 2320-2329.
    • (1973) Cancer Res. , vol.33 , pp. 2320-2329
    • Tan, P.1    Auersperg, N.2
  • 26
    • 0015305826 scopus 로고
    • Synthesis and biological activity of acronycine analogs
    • Schneider, J., Evans, E.L., Grunberg, E., and Fryer, R.I. (1972) Synthesis and Biological Activity of Acronycine Analogs, J. Med. Chem. 15, 266-270.
    • (1972) J. Med. Chem. , vol.15 , pp. 266-270
    • Schneider, J.1    Evans, E.L.2    Grunberg, E.3    Fryer, R.I.4
  • 27
    • 16644397064 scopus 로고    scopus 로고
    • Antiproliferative constituents in plants 14. Coumarins and acridone alkaloids from Boenninghausenia japonica nakai
    • Chaya, N., Terauchi, K., Yamagata, Y., Kinjo, J., and Okabe, H. (2004) Antiproliferative Constituents in Plants 14. Coumarins and Acridone Alkaloids from Boenninghausenia japonica Nakai, Biol Pharm. Bull. 27, 1312-1326.
    • (2004) Biol Pharm. Bull. , vol.27 , pp. 1312-1326
    • Chaya, N.1    Terauchi, K.2    Yamagata, Y.3    Kinjo, J.4    Okabe, H.5
  • 28
    • 14244265661 scopus 로고    scopus 로고
    • Acronycine revisited: Development of benzo[b]acronycine antitumor agents
    • Tillequin, F., and Koch, M. (2005) Acronycine Revisited: Development of Benzo[b]acronycine Antitumor Agents, Ann. Pharm. Fr. 63, 35-43.
    • (2005) Ann. Pharm. Fr. , vol.63 , pp. 35-43
    • Tillequin, F.1    Koch, M.2
  • 29
    • 2142777435 scopus 로고
    • Studies in the area of natural product chemistry. Part LV. Acridone alkaloid glucoside from Ruta graveolens
    • Reisch, J., Rozsa, Z., Szendrei, K., Novak, I., and Minker, E. (1976) Studies in the Area of Natural Product Chemistry. Part LV. Acridone Alkaloid Glucoside from Ruta graveolens, Phytochemistry 15, 240-241.
    • (1976) Phytochemistry , vol.15 , pp. 240-241
    • Reisch, J.1    Rozsa, Z.2    Szendrei, K.3    Novak, I.4    Minker, E.5
  • 30
    • 2142715916 scopus 로고    scopus 로고
    • Specific accumulation and revised structures of acridone alkaloid glucosides in the tips of transformed roots of Ruta graveolens
    • Kuzovkina, I.N., Al'terman, I., and Schneider, B. (2004) Specific Accumulation and Revised Structures of Acridone Alkaloid Glucosides in the Tips of Transformed Roots of Ruta graveolens, Phytochemistry 65, 1095-1100.
    • (2004) Phytochemistry , vol.65 , pp. 1095-1100
    • Kuzovkina, I.N.1    Al'terman, I.2    Schneider, B.3
  • 32
    • 1842715880 scopus 로고    scopus 로고
    • Antileishmanial and antifungal acridone derivatives from the roots of Thamnosma rhodesica
    • Ahua, K.M., Ioset, J.-R., Ransijn, A., Mauël, J., Mavi, S., and Hostettmann, K. (2004) Antileishmanial and Antifungal Acridone Derivatives from the Roots of Thamnosma rhodesica, Phytochemistry 65, 963-968.
    • (2004) Phytochemistry , vol.65 , pp. 963-968
    • Ahua, K.M.1    Ioset, J.-R.2    Ransijn, A.3    Mauël, J.4    Mavi, S.5    Hostettmann, K.6
  • 35
    • 0034058714 scopus 로고    scopus 로고
    • Aporphine glycosides from Stephania cepharantha seeds
    • Kashiwaba, N., Ono, M., Toda, J., Suzuki, H., and Sano, T. (2000) Aporphine Glycosides from Stephania cepharantha Seeds, J. Nat. Prod. 63, 477-479.
    • (2000) J. Nat. Prod. , vol.63 , pp. 477-479
    • Kashiwaba, N.1    Ono, M.2    Toda, J.3    Suzuki, H.4    Sano, T.5
  • 38
    • 0009183721 scopus 로고
    • Two new oxoaporphine alkaloids isolated from Aristolochia tuberosa. I. Structures of tuberosinone and tuberosinone-N-β-D-glucoside
    • Zhu, D., Wang, B., Huang, B., Xu, R., Qiu, Y., Chen, X., and Quan, D. (1983) Two New Oxoaporphine Alkaloids Isolated from Aristolochia tuberosa. I. Structures of Tuberosinone and Tuberosinone-N-β-D-glucoside, Huaxue Xuebao 41, 74-78.
    • (1983) Huaxue Xuebao , vol.41 , pp. 74-78
    • Zhu, D.1    Wang, B.2    Huang, B.3    Xu, R.4    Qiu, Y.5    Chen, X.6    Quan, D.7
  • 39
    • 0007643987 scopus 로고
    • Two new 4,5-dioxoaporphine alkaloids isolated from Aristolochia tuberose
    • Zhu, D., Wang, B., Huang, B., Xu, R., Qiu, Y., and Chen, X. (1982) Two New 4,5-Dioxoaporphine Alkaloids Isolated from Aristolochia tuberose, Heterocycles 17, 345-347.
    • (1982) Heterocycles , vol.17 , pp. 345-347
    • Zhu, D.1    Wang, B.2    Huang, B.3    Xu, R.4    Qiu, Y.5    Chen, X.6
  • 41
    • 0034014079 scopus 로고    scopus 로고
    • Role of natural benzoxazinones in the survival strategy of plants
    • Sicker, D., Frey, M., Schulz, M., and Gierl, A. (2000) Role of Natural Benzoxazinones in the Survival Strategy of Plants, Inter. Rev. Cytol. 198, 319-346.
    • (2000) Inter. Rev. Cytol. , vol.198 , pp. 319-346
    • Sicker, D.1    Frey, M.2    Schulz, M.3    Gierl, A.4
  • 42
    • 0021874560 scopus 로고
    • Benzoxazolinone, 2,4-dihydroxy-1,4-benzoxazin-3-one, and its glucoside from Acanthus mollis seeds inhibit velvetleaf germination and growth
    • Wolf, R.B., Spencer, G.F., and Plattner, R.D. (1985) Benzoxazolinone, 2,4-Dihydroxy-1,4-benzoxazin-3-one, and Its Glucoside from Acanthus mollis Seeds Inhibit Velvetleaf Germination and Growth, J. Nat. Prod. 48, 59-63.
    • (1985) J. Nat. Prod. , vol.48 , pp. 59-63
    • Wolf, R.B.1    Spencer, G.F.2    Plattner, R.D.3
  • 43
    • 0025037697 scopus 로고
    • Studies on acanthaceae. Benzoxazine glucoside and benzoxazolone from Blepharis edulis Pers
    • Chatterjee, A., Sharma, N.J., Basserji, J., and Basa, S.C. (1990) Studies on Acanthaceae. Benzoxazine Glucoside and Benzoxazolone from Blepharis edulis Pers., Indian J. Chem, Sect. B 29, 132-134.
    • (1990) Indian J. Chem, Sect. B , vol.29 , pp. 132-134
    • Chatterjee, A.1    Sharma, N.J.2    Basserji, J.3    Basa, S.C.4
  • 44
    • 0026787442 scopus 로고
    • Isolation and identification via high-performance liquid chromatography and thin-layer chromatography of benzoxazolinone precursors from Consolida orientalis flowers
    • Özden, S., Özden, T., Attila, I., Kücükislamoglu, M., and Okatan, A. (1992) Isolation and Identification via High-Performance Liquid Chromatography and Thin-Layer Chromatography of Benzoxazolinone Precursors from Consolida orientalis Flowers, J. Chromatogr. 609, 402-406.
    • (1992) J. Chromatogr. , vol.609 , pp. 402-406
    • Özden, S.1    Özden, T.2    Attila, I.3    Kücükislamoglu, M.4    Okatan, A.5
  • 45
    • 0029202151 scopus 로고
    • Cyclic hydroxamic acids in dicotyledonous plants
    • Pratt, K., Kumar, P., and Chilton, W.S. (1995) Cyclic Hydroxamic Acids in Dicotyledonous Plants, Biochem. Syst. Ecol. 23, 781-785.
    • (1995) Biochem. Syst. Ecol. , vol.23 , pp. 781-785
    • Pratt, K.1    Kumar, P.2    Chilton, W.S.3
  • 46
    • 12344281587 scopus 로고    scopus 로고
    • Isolation and identification of phototropism-regulating substances benzoxazinoids from maize coleoptiles
    • Hasegawa, T., Yamada, K., Shigemori, H., Miyamoto, K., Ueda, J., and Hasegawa, K. (2004) Isolation and Identification of Phototropism-Regulating Substances Benzoxazinoids from Maize Coleoptiles, Heterocycles 63, 2707-2712.
    • (2004) Heterocycles , vol.63 , pp. 2707-2712
    • Hasegawa, T.1    Yamada, K.2    Shigemori, H.3    Miyamoto, K.4    Ueda, J.5    Hasegawa, K.6
  • 47
    • 29444456609 scopus 로고    scopus 로고
    • (2004) Novel Compounds for Use in Weight Loss and Appetite Suppression in Humans, U.S. Patent Appl. Publ. 38 pp., Continuation in part of U.S. Ser. No. 834,592. US Al 20040930
    • Rosenfeld, M.J., and Forsberg, S.R. (2004) Novel Compounds for Use in Weight Loss and Appetite Suppression in Humans, U.S. Patent Appl. Publ. 38 pp., Continuation in part of U.S. Ser. No. 834,592. US Al 20040930.
    • Rosenfeld, M.J.1    Forsberg, S.R.2
  • 49
    • 0033985405 scopus 로고    scopus 로고
    • Benzoxazinoids-cyclic hydroxamic acids, lactams and their corresponding glucosides in the genus Aphelandra (acanthaceae)
    • Baumeler, A., Hesse, M., and Werner, C. (2000) Benzoxazinoids-Cyclic Hydroxamic Acids, Lactams and Their Corresponding Glucosides in the Genus Aphelandra (Acanthaceae), Phytochemistry 53, 213-222.
    • (2000) Phytochemistry , vol.53 , pp. 213-222
    • Baumeler, A.1    Hesse, M.2    Werner, C.3
  • 50
  • 51
    • 0035900352 scopus 로고    scopus 로고
    • Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus
    • Kanchanapoom, T., Kasai, R., Picheansoonthon, C., and Yamasaki, K. (2001) Megastigmane, Aliphatic Alcohol and Benzoxazinoid Glycosides from Acanthus ebracteatus, Phytochemistry 58, 811-817.
    • (2001) Phytochemistry , vol.58 , pp. 811-817
    • Kanchanapoom, T.1    Kasai, R.2    Picheansoonthon, C.3    Yamasaki, K.4
  • 53
    • 29444437850 scopus 로고
    • Ergot, its history and chemistry
    • Barger, G. (1920) Ergot, Its History and Chemistry, Pharmaceut. J. 105, 470-473.
    • (1920) Pharmaceut. J. , vol.105 , pp. 470-473
    • Barger, G.1
  • 54
    • 0030624683 scopus 로고    scopus 로고
    • Ergot alkaloids-sources, structures and analytical methods
    • Flieger, M., Wurst, M., and Shelby, R. (1997) Ergot Alkaloids-Sources, Structures and Analytical Methods, Folia Microbiol. (Praha) 42, 3-30.
    • (1997) Folia Microbiol. (Praha) , vol.42 , pp. 3-30
    • Flieger, M.1    Wurst, M.2    Shelby, R.3
  • 56
    • 0029557997 scopus 로고
    • Mycotoxins, general view, chemistry and structure
    • Steyn, P.S. (1995) Mycotoxins, General View, Chemistry and Structure, Toxicol. Lett. 82-83, 843-851.
    • (1995) Toxicol. Lett. , vol.82-83 , pp. 843-851
    • Steyn, P.S.1
  • 57
    • 0027447949 scopus 로고
    • Mycotoxins in review
    • Pohland, A.E. (1993) Mycotoxins in Review, Food Addit. Contam. 10, 17-28.
    • (1993) Food Addit. Contam. , vol.10 , pp. 17-28
    • Pohland, A.E.1
  • 58
    • 0037316036 scopus 로고    scopus 로고
    • Ergotamine and dihydroergotamine: History, pharmacology, and efficacy
    • Silerstein, S.D., and McCrory, D.C. (2003) Ergotamine and Dihydroergotamine: History, Pharmacology, and Efficacy, Headache 43, 144-166.
    • (2003) Headache , vol.43 , pp. 144-166
    • Silerstein, S.D.1    McCrory, D.C.2
  • 59
    • 0141649537 scopus 로고    scopus 로고
    • Cabergoline, pramipexole and ropinirole used as monotherapy in early Parkinson's disease: An evidence-based comparison
    • Inzelberg, R., Schechtman, E., and Nisipeanu, P. (2003) Cabergoline, Pramipexole and Ropinirole Used as Monotherapy in Early Parkinson's Disease: An Evidence-Based Comparison, Drugs Aging 20, 847-855.
    • (2003) Drugs Aging , vol.20 , pp. 847-855
    • Inzelberg, R.1    Schechtman, E.2    Nisipeanu, P.3
  • 60
    • 0036911461 scopus 로고    scopus 로고
    • Therapies in development for the treatment of migraine
    • Mucke, H. (2002) Therapies in Development for the Treatment of Migraine, Expert Opin. Investig. Drugs 11, 1813-1820.
    • (2002) Expert Opin. Investig. Drugs , vol.11 , pp. 1813-1820
    • Mucke, H.1
  • 62
    • 0033617717 scopus 로고    scopus 로고
    • Ergoline derivatives: Receptor affinity and selectivity
    • Mantegani, S., Brambilla, E., and Varasi, M. (1999) Ergoline Derivatives: Receptor Affinity and Selectivity, Farmaco 54, 288-296.
    • (1999) Farmaco , vol.54 , pp. 288-296
    • Mantegani, S.1    Brambilla, E.2    Varasi, M.3
  • 63
    • 0014080365 scopus 로고
    • Isolation of elymoclavin-O-β-D-fructoside from cultures of ergot
    • Floss, H.G., Gunther, H., Mothes, U., and Becker, I. (1967) Isolation of Elymoclavin-O-β-D-fructoside from Cultures of Ergot, Z. Naturforsch. [B] 4, 399-402.
    • (1967) Z. Naturforsch. [B] , vol.4 , pp. 399-402
    • Floss, H.G.1    Gunther, H.2    Mothes, U.3    Becker, I.4
  • 65
    • 0025366357 scopus 로고
    • Ergot alkaloid glycosides from saprophytic cultures of Claviceps, II. Chanoclavine I fructosides
    • Flieger, M., Kren, V., Zelenkova, N.F., Sedmera, P., Novak, J., and Sajdl, P. (1990) Ergot Alkaloid Glycosides from Saprophytic Cultures of Claviceps, II. Chanoclavine I Fructosides, J. Nat. Prod. 53, 171-175.
    • (1990) J. Nat. Prod. , vol.53 , pp. 171-175
    • Flieger, M.1    Kren, V.2    Zelenkova, N.F.3    Sedmera, P.4    Novak, J.5    Sajdl, P.6
  • 66
    • 0034872489 scopus 로고    scopus 로고
    • Glycosides in medicine: The role of glycosidic residue in biological activity
    • Kren, V., and Martínková, L. (2001) Glycosides in Medicine: The Role of Glycosidic Residue in Biological Activity, Curr. Med. Chem. 8, 1313-1338.
    • (2001) Curr. Med. Chem. , vol.8 , pp. 1313-1338
    • Kren, V.1    Martínková, L.2
  • 67
    • 14844285470 scopus 로고    scopus 로고
    • Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
    • Somei, M., and Yamada, F. (2005) Simple Indole Alkaloids and Those with a Non-rearranged Monoterpenoid Unit, Nat. Prod. Rep. 22, 73-103.
    • (2005) Nat. Prod. Rep. , vol.22 , pp. 73-103
    • Somei, M.1    Yamada, F.2
  • 68
    • 0036562170 scopus 로고    scopus 로고
    • Bromo- and lodo-containing alkaloids from marine microorganisms and sponges
    • Dembitsky, V.M. (2002) Bromo- and lodo-containing Alkaloids from Marine Microorganisms and Sponges, Bioorg. Khim. (Moscow) 28, 196-208.
    • (2002) Bioorg. Khim. (Moscow) , vol.28 , pp. 196-208
    • Dembitsky, V.M.1
  • 69
    • 85012803695 scopus 로고
    • Indole alkaloids
    • Academic Press, London
    • Saxton, J.E. (1977) Indole Alkaloids, in Alkaloids, Vol. 7, pp. 183-246, Academic Press, London.
    • (1977) Alkaloids , vol.7 , pp. 183-246
    • Saxton, J.E.1
  • 70
    • 29444444416 scopus 로고    scopus 로고
    • Indican metabolism in Polygonum tinctorium
    • Minami, Y. (2001) Indican Metabolism in Polygonum tinctorium, Kagaku To Seibutsu 39, 202-207.
    • (2001) Kagaku to Seibutsu , vol.39 , pp. 202-207
    • Minami, Y.1
  • 72
    • 29444435417 scopus 로고    scopus 로고
    • Extraction of glucoside (indican) from Vietnamese Indigofera for indigo blue dyes
    • Vu, T.T. (1999) Extraction of Glucoside (indican) from Vietnamese Indigofera for Indigo Blue Dyes, Hoa Hoc Va Cong Nghiep Hoa Chat (in Vietnamese) 2, 28-32.
    • (1999) Hoa Hoc Va Cong Nghiep Hoa Chat (In Vietnamese) , vol.2 , pp. 28-32
    • Vu, T.T.1
  • 73
    • 0031715851 scopus 로고    scopus 로고
    • Indoxyl derivatives in woad in relation to medieval indigo production
    • Kokubun, T., Edmonds, J., and John, P. (1998) Indoxyl Derivatives in Woad in Relation to Medieval Indigo Production, Phytochemistry 49, 79-87.
    • (1998) Phytochemistry , vol.49 , pp. 79-87
    • Kokubun, T.1    Edmonds, J.2    John, P.3
  • 74
    • 0035250595 scopus 로고    scopus 로고
    • Chemical constituents of two oriental orchids, Calanthe discolor and C. liukiuensis: Precursor indole glycoside of tryptanthrin and indirubin
    • Murakami, T., Kishi, A., Sakurama, T., Matsuda, H., and Yoshikawa, M. (2001) Chemical Constituents of Two Oriental Orchids, Calanthe discolor and C. liukiuensis: Precursor Indole Glycoside of Tryptanthrin and Indirubin, Heterocycles 54, 957-966.
    • (2001) Heterocycles , vol.54 , pp. 957-966
    • Murakami, T.1    Kishi, A.2    Sakurama, T.3    Matsuda, H.4    Yoshikawa, M.5
  • 75
    • 0031805361 scopus 로고    scopus 로고
    • Novel indole S,O-bisdesmoside, calanthoside, the precursor glycoside of tryptanthrin, indirubin, and isatin, with increasing skin blood flow promoting effects, from two Calanthe species (orchidaceae)
    • Yoshikawa, M., Murakami, T., Kishi, A., Sakurama, T., Matsuda, H., Nomura, M., Matsuda, H., and Kubo, M. (1998) Novel Indole S,O-Bisdesmoside, Calanthoside, the Precursor Glycoside of Tryptanthrin, Indirubin, and Isatin, with Increasing Skin Blood Flow Promoting Effects, from Two Calanthe Species (Orchidaceae), Chem. Pharm. Bull. (Tokyo) 46, 886-888.
    • (1998) Chem. Pharm. Bull. (Tokyo) , vol.46 , pp. 886-888
    • Yoshikawa, M.1    Murakami, T.2    Kishi, A.3    Sakurama, T.4    Matsuda, H.5    Nomura, M.6    Matsuda, H.7    Kubo, M.8
  • 76
    • 0027949845 scopus 로고
    • Indole alkaloids from Brucea mollis var. tonkinensis
    • Ouyang, Y., Koike, K., and Ohmoto, T. (1994) Indole Alkaloids from Brucea mollis var. tonkinensis, Phytochemistry 37, 575-578.
    • (1994) Phytochemistry , vol.37 , pp. 575-578
    • Ouyang, Y.1    Koike, K.2    Ohmoto, T.3
  • 77
    • 0000357062 scopus 로고
    • Isolation and identification of 5-hydroxyindole-3-acetic acid and 5-hydroxytryptophan, major allelopathic aglycons in quackgrass (Agropyron repens L. Beauv.)
    • Hagin, R.D. (1989) Isolation and Identification of 5-Hydroxyindole-3- acetic Acid and 5-Hydroxytryptophan, Major Allelopathic Aglycons in Quackgrass (Agropyron repens L. Beauv.), J. Agric. Food Chem. 37, 1143-1149.
    • (1989) J. Agric. Food Chem. , vol.37 , pp. 1143-1149
    • Hagin, R.D.1
  • 78
    • 0041171193 scopus 로고
    • Indole-3-methanol-β-D-glucoside and indole-3-carboxylic acid-β-D-glucoside are products of indole-3-acetic acid degradation in wheat leaf segments
    • Wiese, G., and Grambow, H.J. (1986) Indole-3-methanol-β-D-glucoside and Indole-3-carboxylic Acid-β-D-glucoside Are Products of Indole-3-acetic Acid Degradation in Wheat Leaf Segments, Phytochemistry 25, 2451-2455.
    • (1986) Phytochemistry , vol.25 , pp. 2451-2455
    • Wiese, G.1    Grambow, H.J.2
  • 79
    • 0022406531 scopus 로고
    • Indole-3-acetic acid catabolism in Zea mays seedlings. Metabolic conversion of oxindole-3-acetic acid to 7-hydroxy-2-oxindole-3-acetic acid 7′-O-β-D-glucopyranoside
    • Nonhebel, H.M., Kruse, L.I., and Bandurski, R.S. (1985) Indole-3-acetic Acid Catabolism in Zea mays Seedlings. Metabolic Conversion of Oxindole-3-acetic Acid to 7-Hydroxy-2-oxindole-3-acetic Acid 7′-O-β-D-Glucopyranoside, J. Biol. Chem. 260, 12685-12689.
    • (1985) J. Biol. Chem. , vol.260 , pp. 12685-12689
    • Nonhebel, H.M.1    Kruse, L.I.2    Bandurski, R.S.3
  • 80
    • 0035974357 scopus 로고    scopus 로고
    • Kahakamides A and B, new neosidomycin metabolites from a marine-derived actinomycete
    • Schumacher, R.W., Harrigan, B.L., and Davidson, B.S. (2001) Kahakamides A and B, New Neosidomycin Metabolites from a Marine-Derived Actinomycete, Tetrahedron Lett. 42, 5133-5135.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 5133-5135
    • Schumacher, R.W.1    Harrigan, B.L.2    Davidson, B.S.3
  • 83
    • 0021164344 scopus 로고
    • A new indole N-glycoside antibiotic SF-2140 from an Actinomadura. I. Taxonomy and fermentation of producing microorganism
    • Tohyama, H., Miyadoh, S., Ito, M., Shomura, T., Ito, T., Ishikawa, T., and Kojima, M. (1984) A New Indole N-Glycoside Antibiotic SF-2140 from an Actinomadura. I. Taxonomy and Fermentation of Producing Microorganism, J. Antibiot. 37, 1144-1148.
    • (1984) J. Antibiot. , vol.37 , pp. 1144-1148
    • Tohyama, H.1    Miyadoh, S.2    Ito, M.3    Shomura, T.4    Ito, T.5    Ishikawa, T.6    Kojima, M.7
  • 84
    • 38049070584 scopus 로고
    • Glucosides of ethyl indole-3-lactate and uroterpenol in Riesling wine
    • Marinos, V.A., Tate, M.E., and Williams, P.J. (1992) Glucosides of Ethyl Indole-3-lactate and Uroterpenol in Riesling Wine, Phytochemistry 31, 2755-2759.
    • (1992) Phytochemistry , vol.31 , pp. 2755-2759
    • Marinos, V.A.1    Tate, M.E.2    Williams, P.J.3
  • 85
    • 0028073170 scopus 로고
    • Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus sp. LL-42D005.1. Isolation and structure determination
    • Ding, W., Williams, D.R., Northcote, P., Siegel, M.M., Tsao, R., Ashcroft, J., Morton, G.O., Alluri, M., and Abranat, D. (1994) Pyrroindomycins, Novel Antibiotics Produced by Streptomyces rugosporus sp. LL-42D005.1. Isolation and Structure Determination, J. Antibiot. 47, 1250-1257.
    • (1994) J. Antibiot. , vol.47 , pp. 1250-1257
    • Ding, W.1    Williams, D.R.2    Northcote, P.3    Siegel, M.M.4    Tsao, R.5    Ashcroft, J.6    Morton, G.O.7    Alluri, M.8    Abranat, D.9
  • 86
    • 0442304059 scopus 로고
    • New oxindole alkaloid glycosides from Uncaria sinensis
    • Liu, H.M., Jiang, Z., and Feng, X.Z. (1993) New Oxindole Alkaloid Glycosides from Uncaria sinensis, Yaoxue Xuebao 28, 849-853.
    • (1993) Yaoxue Xuebao , vol.28 , pp. 849-853
    • Liu, H.M.1    Jiang, Z.2    Feng, X.Z.3
  • 87
    • 4644253305 scopus 로고    scopus 로고
    • New indole alkaloids from the bark of Alstonia scholaris
    • Salim, A.A., Garson, M.J., and Craik, D.J. (2004) New Indole Alkaloids from the Bark of Alstonia scholaris, J. Nat. Prod. 67, 1591-1594.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1591-1594
    • Salim, A.A.1    Garson, M.J.2    Craik, D.J.3
  • 88
    • 0033397710 scopus 로고    scopus 로고
    • β-carboline monoterpenoid glucosides from Palicourea adusta
    • Valverde, J., Tamayo, G., and Hesse, M. (1999) β-Carboline Monoterpenoid Glucosides from Palicourea adusta, Phytochemistry 52, 1485-1489.
    • (1999) Phytochemistry , vol.52 , pp. 1485-1489
    • Valverde, J.1    Tamayo, G.2    Hesse, M.3
  • 89
    • 0028877518 scopus 로고
    • Alkaloids and quassinoids of Brucea mollis var. tonkinensis
    • Ouyang, Y., Mitsunaga, K., Koike, K., and Ohmoto, T. (1995) Alkaloids and Quassinoids of Brucea mollis var. tonkinensis, Phytochemistry 39, 911-913.
    • (1995) Phytochemistry , vol.39 , pp. 911-913
    • Ouyang, Y.1    Mitsunaga, K.2    Koike, K.3    Ohmoto, T.4
  • 90
    • 0028483259 scopus 로고
    • Canthin-6-one alkaloids from Brucea mollis var. tonkinensis
    • Ouyang, Y., Koike, K., and Ohmoto, T. (1994) Canthin-6-one Alkaloids from Brucea mollis var. tonkinensis, Phytochemistry 36, 1543-1546.
    • (1994) Phytochemistry , vol.36 , pp. 1543-1546
    • Ouyang, Y.1    Koike, K.2    Ohmoto, T.3
  • 93
    • 0002537863 scopus 로고    scopus 로고
    • Hunterioside B, a disaccharide carrying monoterpenoid indole alkaloid, from Hunteria zeylanica
    • Takayama, H., Subhadhirasakul, S., Ohmori, O., Kitajima, M., Ponglux, D., and Aimi, N. (1998) Hunterioside B, a Disaccharide Carrying Monoterpenoid Indole Alkaloid, from Hunteria zeylanica, Heterocycles 47, 87-90.
    • (1998) Heterocycles , vol.47 , pp. 87-90
    • Takayama, H.1    Subhadhirasakul, S.2    Ohmori, O.3    Kitajima, M.4    Ponglux, D.5    Aimi, N.6
  • 96
    • 0024347829 scopus 로고
    • Structures of two new alkaloidal glucosides of Nauclea officinalis Pierre ex Pitard
    • Lin, M., Li, S.Z., Liu, X., and Yu, D.Q. (1989) Structures of Two New Alkaloidal Glucosides of Nauclea officinalis Pierre ex Pitard, Yaoxue Xuebao 24, 32-36.
    • (1989) Yaoxue Xuebao , vol.24 , pp. 32-36
    • Lin, M.1    Li, S.Z.2    Liu, X.3    Yu, D.Q.4
  • 97
    • 0022260491 scopus 로고
    • Structure of ophiorines A and B; novel type gluco indole alkaloids isolated from Ophiorrhiza spp
    • Aimi, N., Tsuyuki, T., Murakami, H., Sakai, S., and Haginiwa, J. (1985) Structure of Ophiorines A and B; Novel Type Gluco Indole Alkaloids Isolated from Ophiorrhiza spp, Tetrahedron Lett. 26, 5299-5302.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 5299-5302
    • Aimi, N.1    Tsuyuki, T.2    Murakami, H.3    Sakai, S.4    Haginiwa, J.5
  • 98
    • 0037311005 scopus 로고    scopus 로고
    • Two chromone-secoiridoid glycosides and three indole alkaloid glycosides from Neonauclea sessilifolia
    • Itoh, A., Tanahashi, T., Nagakura, N., and Nishi, T. (2003) Two Chromone-Secoiridoid Glycosides and Three Indole Alkaloid Glycosides from Neonauclea sessilifolia, Phytochemistry 62, 359-369.
    • (2003) Phytochemistry , vol.62 , pp. 359-369
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3    Nishi, T.4
  • 100
    • 0035067858 scopus 로고    scopus 로고
    • New indole alkaloids from Sarcocephalus latifolius
    • Abreu, P., and Pereira, A. (2001) New Indole Alkaloids from Sarcocephalus latifolius, Nat. Prod. Lett. 15, 43-48.
    • (2001) Nat. Prod. Lett. , vol.15 , pp. 43-48
    • Abreu, P.1    Pereira, A.2
  • 101
    • 16644397540 scopus 로고    scopus 로고
    • Bioactive constituents from Chinese natural medicines. XIV. New glycosides of β-carboline type alkaloid, neolignan, and phenylpropanoid from Stellaria dichotoma L. var. lanceolata and their antiallergic activities
    • Morikawa, T., Sun, B., Matsuda, H., Wu, L.J., Harima, S., and Yoshikawa, M. (2004) Bioactive Constituents from Chinese Natural Medicines. XIV. New Glycosides of β-Carboline Type Alkaloid, Neolignan, and Phenylpropanoid from Stellaria dichotoma L. var. lanceolata and Their Antiallergic Activities, Chem. Pharm. Bull. (Tokyo) 52, 1194-1199.
    • (2004) Chem. Pharm. Bull. (Tokyo) , vol.52 , pp. 1194-1199
    • Morikawa, T.1    Sun, B.2    Matsuda, H.3    Wu, L.J.4    Harima, S.5    Yoshikawa, M.6
  • 102
    • 29444445641 scopus 로고
    • Flora Costaricensis, Family No. 202 Rubiaceae, p. 244, Field Museum of Natural History, Chicago
    • Burger, W., and Taylor, C.M. (1993) Fieldiana Botany, New Series No. 33, Flora Costaricensis, Family No. 202 Rubiaceae, p. 244, Field Museum of Natural History, Chicago.
    • (1993) Fieldiana Botany, New Series No. 33
    • Burger, W.1    Taylor, C.M.2
  • 104
    • 0029279356 scopus 로고
    • Amoebicidal compounds from medicinal plants
    • Di Stasi, L.C. (1995) Amoebicidal Compounds from Medicinal Plants, Parassitologia (Brazil) 37, 29-39.
    • (1995) Parassitologia (Brazil) , vol.37 , pp. 29-39
    • Di Stasi, L.C.1
  • 107
    • 0021069585 scopus 로고
    • Part 50 in the series on the validity of the oriental medicines. Hypotensive principles of Uncaria hooks
    • Endo, K., Oshima, Y., and Kikuchi, H. (1983) Part 50 in the Series on the Validity of the Oriental Medicines. Hypotensive Principles of Uncaria Hooks, Planta Med. 49, 188-190.
    • (1983) Planta Med. , vol.49 , pp. 188-190
    • Endo, K.1    Oshima, Y.2    Kikuchi, H.3
  • 108
    • 0033786915 scopus 로고    scopus 로고
    • A new gluco indole alkaloid, 3,4-dehydro-5-carboxystrictosidine, from Peruvian Una de Gato (Uncaria tomentosa)
    • Kitajima, M., Hashimoto, K.I., and Yokoya, M. (2000) A New Gluco Indole Alkaloid, 3,4-Dehydro-5-carboxystrictosidine, from Peruvian Una de Gato (Uncaria tomentosa), Chem. Pharm. Bull. (Tokyo) 48, 1410-1412.
    • (2000) Chem. Pharm. Bull. (Tokyo) , vol.48 , pp. 1410-1412
    • Kitajima, M.1    Hashimoto, K.I.2    Yokoya, M.3
  • 109
    • 0023178261 scopus 로고
    • Production and biological activity of rebeccamycin, a novel antitumor agent
    • Bush, J.A., Long, B.H., Catino, J.J., and Bradner, W.T. (1987) Production and Biological Activity of Rebeccamycin, a Novel Antitumor Agent, J. Antibiot. 40, 668-678.
    • (1987) J. Antibiot. , vol.40 , pp. 668-678
    • Bush, J.A.1    Long, B.H.2    Catino, J.J.3    Bradner, W.T.4
  • 110
    • 0025826820 scopus 로고
    • Morphine 6-glucuronide and morphine 3-glucuronide as molecular chameleons with unexpected lipophilicity
    • Corrupt, P.-A., Testa, B., Bechalany, A., El Tayar, N., Descas, P., and Perrissoud, D. (1991) Morphine 6-Glucuronide and Morphine 3-Glucuronide as Molecular Chameleons with Unexpected Lipophilicity, J. Med. Chem. 34, 1272-1275.
    • (1991) J. Med. Chem. , vol.34 , pp. 1272-1275
    • Corrupt, P.-A.1    Testa, B.2    Bechalany, A.3    El Tayar, N.4    Descas, P.5    Perrissoud, D.6
  • 111
  • 112
    • 0021816422 scopus 로고
    • Isolation and structure of rebeccamycin - A new antitumor antibiotic from Nocardia aerocoligenes
    • Nettleton, D.E., Doyle, T.W., Krishnan, B., Matsumoto, G.K., and Clardy, I. (1985) Isolation and Structure of Rebeccamycin-A New Antitumor Antibiotic from Nocardia aerocoligenes, Tetrahedron Lett. 26, 4011-4014.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 4011-4014
    • Nettleton, D.E.1    Doyle, T.W.2    Krishnan, B.3    Matsumoto, G.K.4    Clardy, I.5
  • 113
    • 0037294445 scopus 로고    scopus 로고
    • Rebeccamycin analogues as anticancer agents
    • Prudhomme, M. (2003) Rebeccamycin Analogues as Anticancer Agents, Eur. J. Med. Chem. 38, 123-140.
    • (2003) Eur. J. Med. Chem. , vol.38 , pp. 123-140
    • Prudhomme, M.1
  • 114
    • 0033755667 scopus 로고    scopus 로고
    • Recent developments of rebeccamycin analogues as topoisomerase I inhibitors and antitumor agents
    • Prudhomme, M. (2000) Recent Developments of Rebeccamycin Analogues as Topoisomerase I Inhibitors and Antitumor Agents, Curr. Med. Chem. 7, 1189-1212.
    • (2000) Curr. Med. Chem. , vol.7 , pp. 1189-1212
    • Prudhomme, M.1
  • 115
    • 1642506144 scopus 로고    scopus 로고
    • Jusbetonin, the first indolo[3,2-b]quinoline alkaloid glycoside, from Justicia betonica
    • Subbaraju, G.V., Kavitha, J., Rajasekhar, D., and Jimenez, J.I. (2004) Jusbetonin, the First Indolo[3,2-b]quinoline Alkaloid Glycoside, from Justicia betonica, J. Nat. Prod. 67, 461-462.
    • (2004) J. Nat. Prod. , vol.67 , pp. 461-462
    • Subbaraju, G.V.1    Kavitha, J.2    Rajasekhar, D.3    Jimenez, J.I.4
  • 118
    • 0037308033 scopus 로고    scopus 로고
    • Recent advances in Betalain research
    • Strack, D., Vogt, T., and Schliemann, W. (2003) Recent Advances in Betalain Research, Phytochemistry 62, 247-269.
    • (2003) Phytochemistry , vol.62 , pp. 247-269
    • Strack, D.1    Vogt, T.2    Schliemann, W.3
  • 120
    • 0242515915 scopus 로고    scopus 로고
    • Antioxidant activity of Betalains from plants of the amaranthaceae
    • Cai, Y., Sun, M., and Corke, H. (2003) Antioxidant Activity of Betalains from Plants of the Amaranthaceae, J. Agric. Food Chem. 57, 2288-2294.
    • (2003) J. Agric. Food Chem. , vol.57 , pp. 2288-2294
    • Cai, Y.1    Sun, M.2    Corke, H.3
  • 121
    • 0005309886 scopus 로고
    • Race differences in the ability to excrete beetroot pigment (betanin)
    • Saldanha, P.H., Magalhaes, L.E., and Horta, W.A. (1960) Race Differences in the Ability to Excrete Beetroot Pigment (betanin), Nature 187, 806.
    • (1960) Nature , vol.187 , pp. 806
    • Saldanha, P.H.1    Magalhaes, L.E.2    Horta, W.A.3
  • 122
    • 0000663162 scopus 로고
    • Betacyanins of the family cactaceae
    • Piattelli, M., and Imperato, F. (1969) Betacyanins of the Family Cactaceae, Phytochemistry 8, 1503-1507.
    • (1969) Phytochemistry , vol.8 , pp. 1503-1507
    • Piattelli, M.1    Imperato, F.2
  • 123
    • 0034877013 scopus 로고    scopus 로고
    • Identification and distribution of simple and acylated betacyanins in the amaranthaceae
    • Cai, Y., Sun, M., and Corke, H. (2001) Identification and Distribution of Simple and Acylated Betacyanins in the Amaranthaceae, J. Agric. Food Chem. 49, 1971-1978.
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 1971-1978
    • Cai, Y.1    Sun, M.2    Corke, H.3
  • 124
    • 2442432692 scopus 로고    scopus 로고
    • Identification of Betalains from petioles of differently colored swiss chard (Beta vulgaris L. ssp. cicla [L.] Alef. cv. bright lights) by high-performance liquid chromatography-electrospray ionization mass spectrometry
    • Kugler, F., Stintzing, P.C., and Carle, R. (2004) Identification of Betalains from Petioles of Differently Colored Swiss Chard (Beta vulgaris L. ssp. cicla [L.] Alef. cv. Bright Lights) by High-Performance Liquid Chromatography-Electrospray Ionization Mass Spectrometry, J. Agric. Food Chem. 52, 2975-2981.
    • (2004) J. Agric. Food Chem. , vol.52 , pp. 2975-2981
    • Kugler, F.1    Stintzing, P.C.2    Carle, R.3
  • 126
    • 12344309479 scopus 로고
    • Betacyanins from Bougainvillea
    • Piattelli, M., and Imperato, F. (1970) Betacyanins from Bougainvillea, Phytochemistry 9, 455-458.
    • (1970) Phytochemistry , vol.9 , pp. 455-458
    • Piattelli, M.1    Imperato, F.2
  • 127
    • 0037308033 scopus 로고    scopus 로고
    • Recent advances in Betalain research
    • Strack, D., Vogt, T., and Schliemann, W. (2003) Recent Advances in Betalain Research, Phytochemistry 62, 247-269.
    • (2003) Phytochemistry , vol.62 , pp. 247-269
    • Strack, D.1    Vogt, T.2    Schliemann, W.3
  • 128
    • 0030003961 scopus 로고    scopus 로고
    • The enediyne antibiotics
    • Smith, A.L., and Nicolaou, K.C. (1996) The Enediyne Antibiotics, J. Med. Chem. 39, 2103-2117.
    • (1996) J. Med. Chem. , vol.39 , pp. 2103-2117
    • Smith, A.L.1    Nicolaou, K.C.2
  • 129
    • 0141919494 scopus 로고    scopus 로고
    • Natural product inspired design of enediyne prodrugs via rearrangement of an allylic double bond
    • Dai, W.M. (2003) Natural Product Inspired Design of Enediyne Prodrugs via Rearrangement of an Allylic Double Bond, Curr. Med. Chem. 10, 2265-2283.
    • (2003) Curr. Med. Chem. , vol.10 , pp. 2265-2283
    • Dai, W.M.1
  • 130
    • 0027319406 scopus 로고
    • Chemistry and biology of natural and designed enediynes
    • Nicolaou, K.C., Smith, A.L., and Yue, E.W. (1993) Chemistry and Biology of Natural and Designed Enediynes, Proc. Natl. Acad. Sci. USA 90, 5881-5888.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 5881-5888
    • Nicolaou, K.C.1    Smith, A.L.2    Yue, E.W.3
  • 131
    • 0037467004 scopus 로고    scopus 로고
    • Shishijimicins A-C, novel enediyne antitumor antibiotics from the ascidian Didemnum proliferum
    • Oku, N., Matsunaga, S., and Fusetani, N. (2003) Shishijimicins A-C, Novel Enediyne Antitumor Antibiotics from the Ascidian Didemnum proliferum, J. Am. Chem. Soc. 125, 2044-2045.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2044-2045
    • Oku, N.1    Matsunaga, S.2    Fusetani, N.3
  • 132
    • 0026452582 scopus 로고
    • Kedarcidin, a new chromoprotein antitumor antibiotic. II. Isolation, purification and physico-chemical properties
    • Hofstead, S.J., Maison, J.A., Malacko, A.R., and Marquardt, H. (1992) Kedarcidin, a New Chromoprotein Antitumor Antibiotic. II. Isolation, Purification and Physico-chemical Properties, J. Antibiot. (Tokyo) 45, 1250-1254.
    • (1992) J. Antibiot. (Tokyo) , vol.45 , pp. 1250-1254
    • Hofstead, S.J.1    Maison, J.A.2    Malacko, A.R.3    Marquardt, H.4
  • 134
    • 0026712564 scopus 로고
    • Antitumor activity of new antitumor antibiotic C1027 and its monoclonal antibody assembled conjugate
    • Shao, R.G., and Zhen, Y.S. (1992) Antitumor Activity of New Antitumor Antibiotic C1027 and Its Monoclonal Antibody Assembled Conjugate, Yao Xue Xue Bao 27, 486-491.
    • (1992) Yao Xue Xue Bao , vol.27 , pp. 486-491
    • Shao, R.G.1    Zhen, Y.S.2
  • 135
    • 0345004890 scopus 로고
    • Antitumor effect of the immunoconjugate composed of antibiotic C1027 and fab fragment from a monoclonal antibody directed against human hepatoma
    • Li, J.Z., Jiang, M., Xue, Y.C., and Zhen, Y.S. (1993) Antitumor Effect of the Immunoconjugate Composed of Antibiotic C1027 and Fab Fragment from a Monoclonal Antibody Directed Against Human Hepatoma, Yao Xue Xue Bao 28, 260-265.
    • (1993) Yao Xue Xue Bao , vol.28 , pp. 260-265
    • Li, J.Z.1    Jiang, M.2    Xue, Y.C.3    Zhen, Y.S.4
  • 136
    • 29444458719 scopus 로고    scopus 로고
    • (2003) The Streptomyces globisporus Gene Cluster for Biosynthesis of the Enediyne Antitumor Antibiotic C-1027 and the Generation of Novel Variants, U.S. Pat. Appl. Publ. 119 pp., U.S. Patent 2003157654 Al 20030821
    • Shen, B., and Liu, W. (2003) The Streptomyces globisporus Gene Cluster for Biosynthesis of the Enediyne Antitumor Antibiotic C-1027 and the Generation of Novel Variants, U.S. Pat. Appl. Publ. 119 pp., U.S. Patent 2003157654 Al 20030821.
    • Shen, B.1    Liu, W.2
  • 139
    • 4444332842 scopus 로고    scopus 로고
    • The effect of body condition on disposition of alkaloids from silvery lupine (Lupinus argenteus pursh) in sheep
    • Lopez-Ortiz, S., Panter, K.E., Pfister, J.A., and Launchbaugh, K.L. (2004) The Effect of Body Condition on Disposition of Alkaloids from Silvery Lupine (Lupinus argenteus Pursh) in Sheep, J. Anim. Sci. 82, 2798-2805.
    • (2004) J. Anim. Sci. , vol.82 , pp. 2798-2805
    • Lopez-Ortiz, S.1    Panter, K.E.2    Pfister, J.A.3    Launchbaugh, K.L.4
  • 140
    • 0023473238 scopus 로고
    • Potential edible lupine poisonings in humans
    • Smith, R.A. (1987) Potential Edible Lupine Poisonings in Humans, Vet. Hum. Toxicol. 29, 444-445.
    • (1987) Vet. Hum. Toxicol. , vol.29 , pp. 444-445
    • Smith, R.A.1
  • 141
    • 7744232650 scopus 로고    scopus 로고
    • Indolizidine and quinolizidine alkaloids
    • Michael, J.P. (2004) Indolizidine and Quinolizidine Alkaloids, Nat. Prod. Rep. 21, 625-649.
    • (2004) Nat. Prod. Rep. , vol.21 , pp. 625-649
    • Michael, J.P.1
  • 144
    • 0007633647 scopus 로고
    • (-)-(trans-4′-β-D-glycopyranosyloxy-3′-methoxycinnamyl) lupinine, a new lupin alkaloid in Lupinus seedlings
    • Murakoshi, I., Toriizuka, K., Haginiwa, J., Ohmiya, S., and Otomasu, H. (1979) (-)-(trans-4′-β-D-Glycopyranosyloxy-3′-methoxycinnamyl) lupinine, a New Lupin Alkaloid in Lupinus Seedlings, Phytochemistry 18, 699-700.
    • (1979) Phytochemistry , vol.18 , pp. 699-700
    • Murakoshi, I.1    Toriizuka, K.2    Haginiwa, J.3    Ohmiya, S.4    Otomasu, H.5
  • 145
    • 4644296823 scopus 로고    scopus 로고
    • History, chemistry and biology of alkaloids from Lobelia inflata
    • Felpin, F.X., and Lebreton, J. (2004) History, Chemistry and Biology of Alkaloids from Lobelia inflata, Tetrahedron 60, 10127-10153.
    • (2004) Tetrahedron , vol.60 , pp. 10127-10153
    • Felpin, F.X.1    Lebreton, J.2
  • 146
    • 0023612372 scopus 로고
    • Further classificalion of skin alkaloids from neotropical poison frogs (dendrobalidae), with a general survey of toxic/noxious substances in the amphibian
    • Daly, J.W., Myers, C.W., and Whillaker, N. (1987) Further Classificalion of Skin Alkaloids from Neotropical Poison Frogs (Dendrobalidae), with a General Survey of Toxic/Noxious Substances in the Amphibian, Toxicon 25, 1023-1095.
    • (1987) Toxicon , vol.25 , pp. 1023-1095
    • Daly, J.W.1    Myers, C.W.2    Whillaker, N.3
  • 147
    • 0033775563 scopus 로고    scopus 로고
    • Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids
    • O'Hagan, D. (2000) Pyrrole, Pyrrolidine, Pyridine, Piperidine and Tropane Alkaloids, Nat. Prod. Rep. 17, 435-446.
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 435-446
    • O'Hagan, D.1
  • 148
    • 1942532837 scopus 로고    scopus 로고
    • Nicoline, its metabolism and an overview of us biological effects
    • Yildiz, D. (2004) Nicoline, Its Metabolism and an Overview of Us Biological Effects, Toxicon 43, 619-632.
    • (2004) Toxicon , vol.43 , pp. 619-632
    • Yildiz, D.1
  • 149
    • 0037832251 scopus 로고    scopus 로고
    • Naturally occurring iminosugars and related compounds: Structure, Distribution, and biological activity
    • Asano, N. (2003) Naturally Occurring Iminosugars and Related Compounds: Structure, Distribution, and Biological Activity, Curr. Top. Med. Chem. 3, 471-484.
    • (2003) Curr. Top. Med. Chem. , vol.3 , pp. 471-484
    • Asano, N.1
  • 150
    • 0002237552 scopus 로고    scopus 로고
    • Taxonomic distribution of iminosugars in plants and their biological activities
    • (Sẗtz, A.E., ed.), Wiley-VCH, Weinheim
    • Simmonds, M.S.J., Kite, G.C., and Porter, E.A. (1999) Taxonomic Distribution of Iminosugars in Plants and Their Biological Activities, in Iminosugars as Glycosidase Inhibitors (Sẗtz, A.E., ed.), pp. 8-30, Wiley-VCH, Weinheim.
    • (1999) IIminosugars As Glycosidase Inhibitors , pp. 8-30
    • Simmonds, M.S.J.1    Kite, G.C.2    Porter, E.A.3
  • 152
    • 0031498895 scopus 로고    scopus 로고
    • A novel glycoside linked piperidine alkaloid from Cyclamen coum
    • Yayli, N., and Baltaci, C. (1997) A Novel Glycoside Linked Piperidine Alkaloid from Cyclamen coum, Turkish J. Chem. 21, 139-143.
    • (1997) Turkish J. Chem. , vol.21 , pp. 139-143
    • Yayli, N.1    Baltaci, C.2
  • 153
    • 84984205480 scopus 로고
    • A glucosidic alkaloid artifact, originated from secoiridoid glucosides from fruits of Ligustrum vulgare L
    • Willems, M. (1988) A Glucosidic Alkaloid Artifact, Originated from Secoiridoid Glucosides from Fruits of Ligustrum vulgare L, Arch. Pharm. (Weinheim) 321, 357-358.
    • (1988) Arch. Pharm. (Weinheim) , vol.321 , pp. 357-358
    • Willems, M.1
  • 154
    • 0043007166 scopus 로고
    • Isolation of a new compounds related to 4-methoxypyridoxine from Albizzia lucida
    • Orsini, F., Pelizzoni, F., Pulici, M., and Verotta, L. (1989) Isolation of a New Compounds Related to 4-Methoxypyridoxine from Albizzia lucida, Gazzetta Chim. Ital. 119, 63-64.
    • (1989) Gazzetta Chim. Ital. , vol.119 , pp. 63-64
    • Orsini, F.1    Pelizzoni, F.2    Pulici, M.3    Verotta, L.4
  • 155
    • 0011895799 scopus 로고
    • Caerulomycin D, a novel glycosidic derivative of 3,4-dihydroxy-2, 2′-dipyridyl 6-aldoxime from Streptomyces caeruleus
    • McInnes, A.G., Smith, D.G., Walter, J.A., Wright, J.L.C., Vining, L.C., and Arsenault, O.P. (1978) Caerulomycin D, a Novel Glycosidic Derivative of 3,4-Dihydroxy-2,2′-dipyridyl 6-Aldoxime from Streptomyces caeruleus, Can. J. Chem. 56, 1836-1842.
    • (1978) Can. J. Chem. , vol.56 , pp. 1836-1842
    • McInnes, A.G.1    Smith, D.G.2    Walter, J.A.3    Wright, J.L.C.4    Vining, L.C.5    Arsenault, O.P.6
  • 156
    • 29444439196 scopus 로고    scopus 로고
    • (1991) Antitumor Glycosides BE-14324 and Their Manufacture with Streptomyces, Jpn. Kokai Tokkyo Koho, 12 pp. Japanese Patent: JP 03081283 A2 19910405 Heisei (in Japanese)
    • Oka, H., Funaishi, K., Kawamura, K., Nakajima, S., Ookura, A., Suda, H., and Okanishi, M. (1991) Antitumor Glycosides BE-14324 and Their Manufacture with Streptomyces, Jpn. Kokai Tokkyo Koho, 12 pp. Japanese Patent: JP 03081283 A2 19910405 Heisei (in Japanese).
    • Oka, H.1    Funaishi, K.2    Kawamura, K.3    Nakajima, S.4    Ookura, A.5    Suda, H.6    Okanishi, M.7
  • 157
    • 0033772332 scopus 로고    scopus 로고
    • Studies on the constituents of Broussonetia species. VII. Four new pyrrolidine alkaloids, broussonetines M, O, P, and Q, as inhibitors of glycosidase, from Broussonetia kazinoki Sieb
    • Shibano, M., Tsukamoto, D., Fujimoto, R., Masui, Y., Sugimoto, H., and Kusano, G. (2000) Studies on the Constituents of Broussonetia Species. VII. Four New Pyrrolidine Alkaloids, Broussonetines M, O, P, and Q, as Inhibitors of Glycosidase, from Broussonetia kazinoki Sieb, Chem. Pharm. Bull. (Tokyo) 48, 1281-1285.
    • (2000) Chem. Pharm. Bull. (Tokyo) , vol.48 , pp. 1281-1285
    • Shibano, M.1    Tsukamoto, D.2    Fujimoto, R.3    Masui, Y.4    Sugimoto, H.5    Kusano, G.6
  • 158
    • 0032919742 scopus 로고    scopus 로고
    • Studies on the constituents of Broussonetia species. V. Two new pyrrolidine alkaloids, broussonetines K and L, as inhibitors of glycosidase, from Broussonetia kazinoki SIEB
    • Shibano, M., Nakamura, S., Motoya, N., and Kusano, G. (1999) Studies on the Constituents of Broussonetia Species. V. Two New Pyrrolidine Alkaloids, Broussonetines K and L, as Inhibitors of Glycosidase, from Broussonetia kazinoki SIEB, Chem. Pharm. Bull. (Tokyo) 47, 472-476.
    • (1999) Chem. Pharm. Bull. (Tokyo) , vol.47 , pp. 472-476
    • Shibano, M.1    Nakamura, S.2    Motoya, N.3    Kusano, G.4
  • 159
    • 0030939363 scopus 로고    scopus 로고
    • Studies on the constituents of Broussonetia species. II. Six new pyrrolidine alkaloids, broussonetine A, B, E, F and broussonetinine a and B, as inhibitors of glycosidases from Broussonetia kazinoki Sieb
    • Shibano, M., Kitagawa, S., Nakamura, S., Akazawa, N., and Kusano, G. (1997) Studies on the Constituents of Broussonetia Species. II. Six New Pyrrolidine Alkaloids, Broussonetine A, B, E, F and Broussonetinine A and B, as Inhibitors of Glycosidases from Broussonetia kazinoki Sieb, Chem. Pharm. Bull. (Tokyo) 45, 700-705.
    • (1997) Chem. Pharm. Bull. (Tokyo) , vol.45 , pp. 700-705
    • Shibano, M.1    Kitagawa, S.2    Nakamura, S.3    Akazawa, N.4    Kusano, G.5
  • 164
    • 0014129723 scopus 로고
    • Studies on Orchidaceae alkaloids. VII. Structure of a glucosidic alkaloid from Malaxis congesta comb. nov. (Rchb. f.)
    • Leander, K., and Liming, B. (1967) Studies on Orchidaceae Alkaloids. VII. Structure of a Glucosidic Alkaloid from Malaxis congesta comb. nov. (Rchb. f.), Tetrahedron Lett. 8, 3477-3478.
    • (1967) Tetrahedron Lett. , vol.8 , pp. 3477-3478
    • Leander, K.1    Liming, B.2
  • 165
    • 0034620695 scopus 로고    scopus 로고
    • Chemotaxonomy and geographical distribution of tropane alkaloids
    • Griffin, W.J., and Lin, D.G. (2000) Chemotaxonomy and Geographical Distribution of Tropane Alkaloids, Phytochemistry 53, 623-637.
    • (2000) Phytochemistry , vol.53 , pp. 623-637
    • Griffin, W.J.1    Lin, D.G.2
  • 168
    • 0037195484 scopus 로고    scopus 로고
    • Analysis of tropane and related alkaloids
    • Dräger, B. (2002) Analysis of Tropane and Related Alkaloids, J. Chromatogr. A. 978, 1-35.
    • (2002) J. Chromatogr. A , vol.978 , pp. 1-35
    • Dräger, B.1
  • 169
    • 0034738364 scopus 로고    scopus 로고
    • Water soluble nortropane alkaloids in crude drugs, edible fruits and vegetables: Biological activities and therapeutic applications
    • Asano, N. (2000) Water Soluble Nortropane Alkaloids in Crude Drugs, Edible Fruits and Vegetables: Biological Activities and Therapeutic Applications, Mech. Ageing Dev. 116, 155-156.
    • (2000) Mech. Ageing Dev. , vol.116 , pp. 155-156
    • Asano, N.1
  • 170
    • 29444453989 scopus 로고    scopus 로고
    • Plant toxins: A historical, evolutionary, economic and toxicological account
    • Naithani, V., Haider, S., and Kakkar, P. (2001) Plant Toxins: A Historical, Evolutionary, Economic and Toxicological Account, J. Ecophysiol. Occupat. Health 1, 339-364.
    • (2001) J. Ecophysiol. Occupat. Health , vol.1 , pp. 339-364
    • Naithani, V.1    Haider, S.2    Kakkar, P.3
  • 172
    • 0029881664 scopus 로고    scopus 로고
    • 1, a novel nortropane alkaloid with a bridgehead amino group from Hyoscyamus niger: Structure determination and glycosidase inhibitory activities
    • 1, a Novel Nortropane Alkaloid with a Bridgehead Amino Group from Hyoscyamus niger: Structure Determination and Glycosidase Inhibitory Activities, Carbohydr. Res. 284, 169-178.
    • (1996) Carbohydr. Res. , vol.284 , pp. 169-178
    • Asano, N.1    Kato, A.2    Yokoyama, Y.3    Miyauchi, M.4    Yamamoto, M.5    Kizu, H.6    Matsui, K.7
  • 174
    • 0033151364 scopus 로고    scopus 로고
    • The chemical systematics of alkaloids: A review emphasising the contribution of Robert Hegnauer
    • Waterman, P.O. (1999) The Chemical Systematics of Alkaloids: A Review Emphasising the Contribution of Robert Hegnauer, Biochem. Syst. Ecol. 27, 395-406.
    • (1999) Biochem. Syst. Ecol. , vol.27 , pp. 395-406
    • Waterman, P.O.1
  • 175
    • 17544363299 scopus 로고    scopus 로고
    • Malaria: Severe, life threatening
    • Omari, A., and Garner, P. (2004) Malaria: Severe, Life Threatening, Clin. Evid. 11, 1047-1057.
    • (2004) Clin. Evid. , vol.11 , pp. 1047-1057
    • Omari, A.1    Garner, P.2
  • 177
    • 7744242263 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • Michael, J.P. (2004) Quinoline, Quinazoline and Acridone Alkaloids, Nat. Prod. Rep. 21, 650-668.
    • (2004) Nat. Prod. Rep. , vol.21 , pp. 650-668
    • Michael, J.P.1
  • 178
    • 0042812136 scopus 로고    scopus 로고
    • Stephacidin B - A new stage of complexity within prenylated indole alkaloids from fungi
    • Von Nussbaum, F. (2003) Stephacidin B-A New Stage of Complexity Within Prenylated Indole Alkaloids from Fungi, Angew. Chem. Int. Ed. Engl. 42, 3068-3071.
    • (2003) Angew. Chem. Int. Ed. Engl. , vol.42 , pp. 3068-3071
    • Von Nussbaum, F.1
  • 180
    • 0031194996 scopus 로고    scopus 로고
    • Two quinoline alkaloids from the caribbean cyanobacterium Lyngbya majuscula
    • Orjala, J., and Gerwick, W.H. (1997) Two Quinoline Alkaloids from the Caribbean Cyanobacterium Lyngbya majuscula, Phytochemistry 45, 1087-1090.
    • (1997) Phytochemistry , vol.45 , pp. 1087-1090
    • Orjala, J.1    Gerwick, W.H.2
  • 181
    • 3042596586 scopus 로고    scopus 로고
    • Two new quinoline glycoalkaloids from Echinops gmelinii
    • Su, Y.-F., Luo, Y., Guo, C.-Y., and Guo, D.-A. (2004) Two New Quinoline Glycoalkaloids from Echinops gmelinii, J. Asian Nat. Prod. Res. 6, 223-227.
    • (2004) J. Asian Nat. Prod. Res. , vol.6 , pp. 223-227
    • Su, Y.-F.1    Luo, Y.2    Guo, C.-Y.3    Guo, D.-A.4
  • 182
    • 29444451717 scopus 로고
    • Haplosinine, a new furanoquinoline glycoalkaloid from Haplophyllum perforatum
    • Rasulova, K.A., Bessonova, I.A., Yagudaev, M.R., and Yunusov, S.Y. (1987) Haplosinine, a New Furanoquinoline Glycoalkaloid from Haplophyllum perforatum, Khim. Prirod. Soed. 6, 876-879.
    • (1987) Khim. Prirod. Soed. , vol.6 , pp. 876-879
    • Rasulova, K.A.1    Bessonova, I.A.2    Yagudaev, M.R.3    Yunusov, S.Y.4
  • 183
    • 0032698594 scopus 로고    scopus 로고
    • 20-O-β-glucopyranosyl camptothecin from Mostuea brunonis: A potential camptothecin pro-drug with improved solubility
    • Dai, J.R., Hallock, Y.F., Cardellina, J.H., II, and Boyd, M.R. (1999) 20-O-β-Glucopyranosyl Camptothecin from Mostuea brunonis: A Potential Camptothecin Pro-drug with Improved Solubility, J. Nat. Prod. 62, 1427-1429.
    • (1999) J. Nat. Prod. , vol.62 , pp. 1427-1429
    • Dai, J.R.1    Hallock, Y.F.2    Cardellina II, J.H.3    Boyd, M.R.4
  • 185
    • 29444436214 scopus 로고
    • Thalictrum alkaloids. VI. (-)-Veronamine, a glycosidic benzylisoquinoline
    • Shamma, M., Kelly, M.G., and Podczasy, M.A., Sr. (1969) Thalictrum Alkaloids. VI. (-)-Veronamine, a Glycosidic Benzylisoquinoline, Tetrahedron Lett. 10, 4951-4954.
    • (1969) Tetrahedron Lett. , vol.10 , pp. 4951-4954
    • Shamma, M.1    Kelly, M.G.2    Podczasy Sr., M.A.3
  • 186
    • 0016415348 scopus 로고
    • Alangiside, the monoterpenoid alkaloidal glycoside from Alangium lamarckii Thw
    • Shoeb, A., Raj, K., Kapil, R.S., and Popli, S.P. (1975) Alangiside, the Monoterpenoid Alkaloidal Glycoside from Alangium lamarckii Thw, J. Chem. Soc. Perkin I 13, 1245-1248.
    • (1975) J. Chem. Soc. Perkin I , vol.13 , pp. 1245-1248
    • Shoeb, A.1    Raj, K.2    Kapil, R.S.3    Popli, S.P.4
  • 187
    • 0037116409 scopus 로고    scopus 로고
    • Tetrahydroisoquinolinemonoterpene glycosides from Cephaelis acuminata
    • Itoh, A., Baba, Y., Tanahashi, T., and Nagakura, N. (2002) Tetrahydroisoquinolinemonoterpene Glycosides from Cephaelis acuminata, Phytochemistry 59, 91-97.
    • (2002) Phytochemistry , vol.59 , pp. 91-97
    • Itoh, A.1    Baba, Y.2    Tanahashi, T.3    Nagakura, N.4
  • 188
    • 0031450685 scopus 로고    scopus 로고
    • Five tetrahydroisoquinoline-monoterpene glycosides with a disaccharide moiety from Alangium lamarckii
    • Itoh, A., Tanahashi, T., and Nagakura, N. (1997) Five Tetrahydroisoquinoline-monoterpene Glycosides with a Disaccharide Moiety from Alangium lamarckii, Phytochemistry 46, 1225-1229.
    • (1997) Phytochemistry , vol.46 , pp. 1225-1229
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3
  • 189
    • 0030067507 scopus 로고    scopus 로고
    • Acylated tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii
    • Itoh, A., Tanahashi, T., and Nagakura, N. (1996) Acylated Tetrahydroisoquinoline-monoterpene Glucosides from Alangium lamarckii, Phytochemistry 41, 651-656.
    • (1996) Phytochemistry , vol.41 , pp. 651-656
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3
  • 191
    • 0000858699 scopus 로고    scopus 로고
    • Isolation of two unusual tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii as possible intermediates in the nonenzymic formation of alangimarine from alangiside
    • Itoh, A., Tanahashi, T., and Nagakura, N. (1998) Isolation of Two Unusual Tetrahydroisoquinoline-monoterpene Glucosides from Alangium lamarckii as Possible Intermediates in the Nonenzymic Formation of Alangimarine from Alangiside, Heterocycles 48, 499-505.
    • (1998) Heterocycles , vol.48 , pp. 499-505
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3
  • 192
    • 0007884180 scopus 로고
    • Four tetrahydroisoquinoline-monoterpene glucosides from Cephaelis ipecacuanha
    • Nagakura, N., Itoh, A., and Tanahashi, T. (1993) Four Tetrahydroisoquinoline-monoterpene Glucosides from Cephaelis ipecacuanha, Phytochemistry 32, 761-765.
    • (1993) Phytochemistry , vol.32 , pp. 761-765
    • Nagakura, N.1    Itoh, A.2    Tanahashi, T.3
  • 193
    • 0027521821 scopus 로고
    • Dauricoside, a new glycosidal alkaloid having an inhibitory activity against blood-platelet aggregation
    • Hu, S., Xu, S., Yao, X., Cui, C.B., Tezuka, Y., and Kikuchi, T. (1993) Dauricoside, a New Glycosidal Alkaloid Having an Inhibitory Activity Against Blood-Platelet Aggregation, Chem. Pharm. Bull. (Tokyo) 41, 1866-1868.
    • (1993) Chem. Pharm. Bull. (Tokyo) , vol.41 , pp. 1866-1868
    • Hu, S.1    Xu, S.2    Yao, X.3    Cui, C.B.4    Tezuka, Y.5    Kikuchi, T.6
  • 194
    • 0008743753 scopus 로고    scopus 로고
    • Utilization of alkaloids in modern medicine
    • (Roberts, M., and Wink, M., eds.), Plenum Press, New York
    • Schmeller, T., and Wink, M. (1998) Utilization of Alkaloids in Modern Medicine, in Alkaloids-Biochemistry, Ecology and Medicinal Applications (Roberts, M., and Wink, M., eds.), pp. 435-459, Plenum Press, New York.
    • (1998) Alkaloids-Biochemistry, Ecology and Medicinal Applications , pp. 435-459
    • Schmeller, T.1    Wink, M.2
  • 195
    • 0015379922 scopus 로고
    • Chemotherapy of tumors. II. Chemical review of natural neoplastic agents: Alkaloids, their analogs and other products extracted from plants
    • Artico, M. (1972) Chemotherapy of Tumors. II. Chemical Review of Natural Neoplastic Agents: Alkaloids, Their Analogs and Other Products Extracted from Plants, Farmaco 27, 683-712.
    • (1972) Farmaco , vol.27 , pp. 683-712
    • Artico, M.1
  • 196
    • 0017738416 scopus 로고
    • Toxicology of Ipecac: A review
    • Manno, B.R., and Manno, J.E. (1977) Toxicology of Ipecac: A Review, Clin. Toxicol. 10, 221-242.
    • (1977) Clin. Toxicol. , vol.10 , pp. 221-242
    • Manno, B.R.1    Manno, J.E.2
  • 198
    • 0016291233 scopus 로고
    • Recent progress in the biochemistry of plant steroids other than sterols (saponins, glycoalkaloids, pregnane derivatives, cardiac glycosides, and sex hormones)
    • Heftmann, E. (1974) Recent Progress in the Biochemistry of Plant Steroids Other Than Sterols (saponins, glycoalkaloids, pregnane derivatives, cardiac glycosides, and sex hormones), Lipids 9, 626-639.
    • (1974) Lipids , vol.9 , pp. 626-639
    • Heftmann, E.1
  • 200
    • 0030477673 scopus 로고    scopus 로고
    • Steroidal glycoalkaloids: Nature and consequences of bioactivity
    • Roddick, J.G. (1996) Steroidal Glycoalkaloids: Nature and Consequences of Bioactivity, Adv. Exp. Med. Biol. 404, 277-295.
    • (1996) Adv. Exp. Med. Biol. , vol.404 , pp. 277-295
    • Roddick, J.G.1
  • 201
    • 0037048751 scopus 로고    scopus 로고
    • Tomato glycoalkaloids: Role in the plant and in the diet
    • Friedman, M. (2002) Tomato Glycoalkaloids: Role in the Plant and in the Diet, J. Agric. Food Chem. 50, 5751-5780.
    • (2002) J. Agric. Food Chem. , vol.50 , pp. 5751-5780
    • Friedman, M.1
  • 203
    • 0348023678 scopus 로고
    • Teratogenic constituents of potatoes
    • Kuc, J. (1975) Teratogenic Constituents of Potatoes, Recent Adv. Phytochem. 9, 139-150.
    • (1975) Recent Adv. Phytochem. , vol.9 , pp. 139-150
    • Kuc, J.1
  • 204
    • 9644303108 scopus 로고    scopus 로고
    • Effects of steroidal glycoalkaloids from potatoes (Solanum tuberosum) on in vitro bovine embryo development
    • Wang, S., Panter, K.E., Gaffield, W., Evans, R.C., and Bunch, T.D. (2005) Effects of Steroidal Glycoalkaloids from Potatoes (Solanum tuberosum) on in vitro Bovine Embryo Development, Anim. Reprod. Sci. 85, 243-250.
    • (2005) Anim. Reprod. Sci. , vol.85 , pp. 243-250
    • Wang, S.1    Panter, K.E.2    Gaffield, W.3    Evans, R.C.4    Bunch, T.D.5
  • 208
    • 23744506485 scopus 로고    scopus 로고
    • Anticarcinogenic effects of glycoalkaloids from potatoes against human cervical, liver, lymphoma, and stomach cancer cells
    • Friedman, M., Lee, K.R., Kim, H.J., Lee, I.S., and Kozukue, N. (2005) Anticarcinogenic Effects of Glycoalkaloids from Potatoes Against Human Cervical, Liver, Lymphoma, and Stomach Cancer Cells, J. Agric. Food Chem. 53, 6162-6169, 8420.
    • (2005) J. Agric. Food Chem. , vol.53 , pp. 6162-6169
    • Friedman, M.1    Lee, K.R.2    Kim, H.J.3    Lee, I.S.4    Kozukue, N.5
  • 209
    • 7444247890 scopus 로고    scopus 로고
    • Analysis of biologically active compounds in potatoes (Solanum tuberosum), tomatoes (Lycopersicon esculentum), and Jimson weed (Datura stramonium) seeds
    • Friedman, M. (2004) Analysis of Biologically Active Compounds in Potatoes (Solanum tuberosum), Tomatoes (Lycopersicon esculentum), and Jimson Weed (Datura stramonium) Seeds, J. Chromatogr. A. 1054, 143-155.
    • (2004) J. Chromatogr. A , vol.1054 , pp. 143-155
    • Friedman, M.1
  • 210
    • 0023132749 scopus 로고
    • Antitumor effects of glycoalkaloids isolated from Solanum sodomaeum
    • Cham, B.E., Gilliver, M., and Wilson, L. (1987) Antitumor Effects of Glycoalkaloids Isolated from Solanum sodomaeum, Planta Med. 53, 34-36.
    • (1987) Planta Med. , vol.53 , pp. 34-36
    • Cham, B.E.1    Gilliver, M.2    Wilson, L.3
  • 211
    • 2942537986 scopus 로고    scopus 로고
    • Arudonine, an allelopathic steroidal glycoalkaloid from the root bark of Solanum arundo mattel
    • Fukuhara, K., Shimizu, K., and Kubo, I. (2004) Arudonine, an Allelopathic Steroidal Glycoalkaloid from the Root Bark of Solanum arundo Mattel, Phytochemistry 65, 1283-1286.
    • (2004) Phytochemistry , vol.65 , pp. 1283-1286
    • Fukuhara, K.1    Shimizu, K.2    Kubo, I.3
  • 212
    • 0035111230 scopus 로고    scopus 로고
    • Steroidal glycoside and glycoalkaloid from Solanum lyratum
    • Ye, W.-C., Wang, H., Zhao, S.-X., and Che, C.-T. (2001) Steroidal Glycoside and Glycoalkaloid from Solanum lyratum, Biochem. Syst. Ecol. 29, 421-423.
    • (2001) Biochem. Syst. Ecol. , vol.29 , pp. 421-423
    • Ye, W.-C.1    Wang, H.2    Zhao, S.-X.3    Che, C.-T.4
  • 214
    • 1642424212 scopus 로고    scopus 로고
    • Steroidal alkaloid glycosides from tomato (Lycopersicon esculentum)
    • Yahara, S., Uda, N., Yoshio, E., and Yae, E. (2004) Steroidal Alkaloid Glycosides from Tomato (Lycopersicon esculentum), J. Nat. Prod. 67, 500-502.
    • (2004) J. Nat. Prod. , vol.67 , pp. 500-502
    • Yahara, S.1    Uda, N.2    Yoshio, E.3    Yae, E.4
  • 215
    • 1342265152 scopus 로고    scopus 로고
    • Possible industrial applications of genus Solanum in twenty-first century: A review
    • Amir, M., and Kumar, S. (2004) Possible Industrial Applications of Genus Solanum in Twenty-first Century: A Review, J. Scient. Indust. Res. 63, 116-124.
    • (2004) J. Scient. Indust. Res. , vol.63 , pp. 116-124
    • Amir, M.1    Kumar, S.2
  • 216
    • 0000803902 scopus 로고
    • Rare phenazine L-quinovose esters from a marine actinomycete
    • Pathirana, C., Jensen, P.R., Dwight, R., and Fenical, W. (1992) Rare Phenazine L-Quinovose Esters from a Marine Actinomycete, J. Org. Chem. 57, 740-742.
    • (1992) J. Org. Chem. , vol.57 , pp. 740-742
    • Pathirana, C.1    Jensen, P.R.2    Dwight, R.3    Fenical, W.4
  • 217
    • 0021241827 scopus 로고
    • Biological activities of broad bean (Vicia faba L.) extracts cultivated in South Anatolia in favism sensitive subjects
    • Vural, N., and Sardas, S. (1984) Biological Activities of Broad Bean (Vicia faba L.) Extracts Cultivated in South Anatolia in Favism Sensitive Subjects, Toxicology 31, 175-179.
    • (1984) Toxicology , vol.31 , pp. 175-179
    • Vural, N.1    Sardas, S.2
  • 218
    • 84986596104 scopus 로고
    • Variability of amino acids, protein, vicine and convicine in Vicia faba (L)
    • Lattanzio, V., Bianco, V.V., Crivelli, G., and Miccolis, V. (1983) Variability of Amino Acids, Protein, Vicine and Convicine in Vicia faba (L), J. Food Sci. 48, 992-993.
    • (1983) J. Food Sci. , vol.48 , pp. 992-993
    • Lattanzio, V.1    Bianco, V.V.2    Crivelli, G.3    Miccolis, V.4
  • 219
    • 0011737603 scopus 로고
    • Structures of two novel monoterpene alkaloid glucosides from Lonicera xylosteum L
    • Chaudhuri, R.K., Sticher, O., and Winkler, T. (1981) Structures of Two Novel Monoterpene Alkaloid Glucosides from Lonicera xylosteum L, Tetrahedron Lett. 22, 559-562.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 559-562
    • Chaudhuri, R.K.1    Sticher, O.2    Winkler, T.3
  • 220
    • 0012016446 scopus 로고
    • Xylostosidine: The first of a new class of monoterpene alkaloid glycosides from Lonicera xylosteum
    • Chaudhuri, R.K., Sticher, O., and Winkler, T. (1980) Xylostosidine: The First of a New Class of Monoterpene Alkaloid Glycosides from Lonicera xylosteum, Helv. Chim. Acta 63, 1045-1047.
    • (1980) Helv. Chim. Acta , vol.63 , pp. 1045-1047
    • Chaudhuri, R.K.1    Sticher, O.2    Winkler, T.3
  • 222
    • 0345732576 scopus 로고    scopus 로고
    • Daphcalycinosidines A and B, new iridoid-alkaloids from Daphniphyllum calycinum
    • El Bitar, H., Nguyen, V.H., Gramain, A., Sévenet, T., and Bodo, B. (2004) Daphcalycinosidines A and B, New Iridoid-Alkaloids from Daphniphyllum calycinum, Tetrahedron Lett. 45, 515-518.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 515-518
    • El Bitar, H.1    Nguyen, V.H.2    Gramain, A.3    Sévenet, T.4    Bodo, B.5
  • 224
    • 0020406731 scopus 로고
    • Isolation of neosurugatoxin from the Japanese ivory shell, Babylonia japonica
    • Kosuge, T., Tsuji, K., and Hirai, K. (1982) Isolation of Neosurugatoxin from the Japanese Ivory Shell, Babylonia japonica, Chem. Pharm. Bull. (Tokyo) 30, 3255-3259.
    • (1982) Chem. Pharm. Bull. (Tokyo) , vol.30 , pp. 3255-3259
    • Kosuge, T.1    Tsuji, K.2    Hirai, K.3
  • 225
    • 0022834019 scopus 로고
    • Schumanniofoside, the antisnake venom principle from the stem bark of Schumanniophyton magnificum harms
    • Akunyili, D.N., and Akubue, P.I. (1986) Schumanniofoside, the Antisnake Venom Principle from the Stem Bark of Schumanniophyton magnificum Harms, J. Ethnopharmacol. 18, 167-172.
    • (1986) J. Ethnopharmacol. , vol.18 , pp. 167-172
    • Akunyili, D.N.1    Akubue, P.I.2
  • 226
    • 29444441424 scopus 로고
    • Bakankosine, a new glucoside hydrolyzed by emulsin, found in the seeds of a Strychnos from Madagascar
    • Bourquelot, E., and Herissey, H. (1907) Bakankosine, a New Glucoside Hydrolyzed by Emulsin, Found in the Seeds of a Strychnos from Madagascar, Compt. Rend. Acad. Sci. Paris 144, 575-577.
    • (1907) Compt. Rend. Acad. Sci. Paris , vol.144 , pp. 575-577
    • Bourquelot, E.1    Herissey, H.2
  • 227
    • 0017162510 scopus 로고
    • Iridoids. VII. Synthesis and structural proof of bakankosine
    • Tietze, L.F. (1976) Iridoids. VII. Synthesis and Structural Proof of Bakankosine, Tetrahedron Lett. 29, 2535-2538.
    • (1976) Tetrahedron Lett. , vol.29 , pp. 2535-2538
    • Tietze, L.F.1


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