메뉴 건너뛰기




Volumn , Issue , 2013, Pages 479-522

Amaryllidaceae alkaloids

Author keywords

Alkaloid; Amaryllidaceae; Biological activity; Biosynthesis; Tyrosine

Indexed keywords


EID: 85027835702     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-642-22144-6_18     Document Type: Chapter
Times cited : (28)

References (169)
  • 3
    • 0033245205 scopus 로고    scopus 로고
    • Phylogenetic relationships of Amaryllidaceae based on matK sequence data
    • Ito M, Kawamoto A, Kita Y, Yukawa T, Kurita S (1999) Phylogenetic relationships of Amaryllidaceae based on matK sequence data. J Plant Res 112:207
    • (1999) J Plant Res , vol.112 , pp. 207
    • Ito, M.1    Kawamoto, A.2    Kita, Y.3    Yukawa, T.4    Kurita, S.5
  • 4
    • 70350220743 scopus 로고    scopus 로고
    • A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae
    • Chase MW, Reveal JL, Fay MF (2009) A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae. Bot J Linn Soc 161:132
    • (2009) Bot J Linn Soc , vol.161 , pp. 132
    • Chase, M.W.1    Reveal, J.L.2    Fay, M.F.3
  • 5
    • 77952303290 scopus 로고    scopus 로고
    • Chemistry and biology of Pancratium alkaloids
    • Cordell GA, Elsevier Scientific Publishing, Amsterdam
    • Cedron, JC, Del Arco-Aguilar M, Estevez-Braun A, Ravelo AG (2010) Chemistry and biology of Pancratium alkaloids. In: Cordell GA (ed) The alkaloids, vol 68. Elsevier Scientific Publishing, Amsterdam
    • (2010) The Alkaloids , vol.68
    • Cedron, J.C.1    Del Arco-Aguilar, M.2    Estevez-Braun, A.3    Ravelo, A.G.4
  • 6
    • 77952312984 scopus 로고    scopus 로고
    • Galanthamine from Galanthus and other Amaryllidaceae - chemistry and biology based on tradition use
    • Cordell GA, Elsevier Scientific Publishing, Amsterdam
    • Heinrich M (2010) Galanthamine from Galanthus and other Amaryllidaceae - chemistry and biology based on tradition use. In: Cordell GA (ed) The alkaloids, vol 68. Elsevier Scientific Publishing, Amsterdam
    • (2010) The Alkaloids , vol.68
    • Heinrich, M.1
  • 7
    • 77952313393 scopus 로고    scopus 로고
    • Galanthamine production by Leucojum aestivum cultures in vitro
    • Cordell GA, Elsevier Scientific Publishing, Amsterdam
    • Stanilova MI, Molle ED, Yanev SG (2010) Galanthamine production by Leucojum aestivum cultures in vitro. In: Cordell GA (ed) The alkaloids, vol 68. Elsevier Scientific Publishing, Amsterdam
    • (2010) The Alkaloids , vol.68
    • Stanilova, M.I.1    Molle, E.D.2    Yanev, S.G.3
  • 8
    • 33947377017 scopus 로고    scopus 로고
    • New skeletons and new concepts in Amaryllidaceae alkaloids
    • Unver N (2007) New skeletons and new concepts in Amaryllidaceae alkaloids. Phytochem Rev 6:125
    • (2007) Phytochem Rev , vol.6 , pp. 125
    • Unver, N.1
  • 9
    • 34250756893 scopus 로고    scopus 로고
    • Chemistry and biology aspects of Narcissus alkaloids
    • Cordell GA, Elsevier Scientific Publishing, Amsterdam
    • Bastida J, Lavilla R, Viladomat F (2006) Chemistry and biology aspects of Narcissus alkaloids. In: Cordell GA (ed) The alkaloids, vol 63. Elsevier Scientific Publishing, Amsterdam
    • (2006) The Alkaloids , vol.63
    • Bastida, J.1    Lavilla, R.2    Viladomat, F.3
  • 10
    • 47249124531 scopus 로고    scopus 로고
    • Chemistry, biology, and medicinal potential of narciclasine and its congeners
    • Kornienko A, Evidente A (2008) Chemistry, biology, and medicinal potential of narciclasine and its congeners. Chem Rev 108:1982
    • (2008) Chem Rev , vol.108 , pp. 1982
    • Kornienko, A.1    Evidente, A.2
  • 11
    • 33746897346 scopus 로고    scopus 로고
    • Chemistry and synthesis of highly oxygenated alkaloids from Amaryllidaceae: Lycoricidine, narciclasine, pancratistatin and analogues
    • Chapleur Y, Chretien F, Ibn Ahmed S, Khaldi M (2006) Chemistry and synthesis of highly oxygenated alkaloids from Amaryllidaceae: lycoricidine, narciclasine, pancratistatin and analogues. Curr Org Synth 3:341
    • (2006) Curr Org Synth , vol.3 , pp. 341
    • Chapleur, Y.1    Chretien, F.2    Ibn Ahmed, S.3    Khaldi, M.4
  • 13
    • 14644422595 scopus 로고    scopus 로고
    • Synthesis of Amaryllidaceae constituents - an update
    • Rinner U, Hudlicky T (2005) Synthesis of Amaryllidaceae constituents - an update. Synlett 365-387
    • (2005) Synlett , pp. 365-387
    • Rinner, U.1    Hudlicky, T.2
  • 14
    • 2442455266 scopus 로고    scopus 로고
    • Narcissus and daffodil-the genus Narcissus
    • Hardman R, Taylor & Francois, London
    • Hanks GR (2002) Narcissus and daffodil-the genus Narcissus. In: Hardman R (ed) Medicinal and aromatic plants-industrial profiles, vol 21. Taylor & Francois, London
    • (2002) Medicinal and Aromatic Plants-Industrial Profiles , vol.21
    • Hanks, G.R.1
  • 16
    • 33746930690 scopus 로고    scopus 로고
    • Recent advances in the total synthesis of Amaryllidaceae alkaloids
    • Sundaresan P, Regina TM (2001) Recent advances in the total synthesis of Amaryllidaceae alkaloids. Alkaloids: Chem Biol Perspect 15:433
    • (2001) Alkaloids: Chem Biol Perspect , vol.15 , pp. 433
    • Sundaresan, P.1    Regina, T.M.2
  • 17
    • 77957033352 scopus 로고
    • The Amaryllidaceae alkaloids
    • Brossi A (ed.), Academic, New York
    • Martin SF (1987) The Amaryllidaceae alkaloids. In: Brossi A (ed.) The alkaloids, vol 30. Academic, New York
    • (1987) The Alkaloids , vol.30
    • Martin, S.F.1
  • 18
    • 0000427207 scopus 로고
    • Crinum alkaloids: Their chemistry and biology
    • Ghosal S, Saini KS, Razdan S (1985) Crinum alkaloids: their chemistry and biology. Phytochemistry 24:2141
    • (1985) Phytochemistry , vol.24 , pp. 2141
    • Ghosal, S.1    Saini, K.S.2    Razdan, S.3
  • 19
    • 77956708370 scopus 로고    scopus 로고
    • The Amaryllidaceae alkaloids
    • Cordell GA, Academic, New York
    • Hoshino O (1998) The Amaryllidaceae alkaloids. In: Cordell GA (ed) The alkaloids chemistry and pharmacology, vol 51. Academic, New York, pp 323-424
    • (1998) The Alkaloids Chemistry and Pharmacology , vol.51 , pp. 323-424
    • Hoshino, O.1
  • 20
    • 80052059081 scopus 로고    scopus 로고
    • Amaryllidaceae and sceletium alkaloids
    • Jin Z (2011) Amaryllidaceae and sceletium alkaloids. Nat Prod Rep 28:1126
    • (2011) Nat Prod Rep , vol.28 , pp. 1126
    • Jin, Z.1
  • 21
    • 61449118878 scopus 로고    scopus 로고
    • Amaryllidaceae and sceletium alkaloids
    • Jin Z (2009) Amaryllidaceae and sceletium alkaloids. Nat Prod Rep 26:363
    • (2009) Nat Prod Rep , vol.26 , pp. 363
    • Jin, Z.1
  • 22
    • 34547216418 scopus 로고    scopus 로고
    • Amaryllidaceae and sceletium alkaloids
    • Jin Z (2007) Amaryllidaceae and sceletium alkaloids. Nat Prod Rep 24:886
    • (2007) Nat Prod Rep , vol.24 , pp. 886
    • Jin, Z.1
  • 23
    • 14844285469 scopus 로고    scopus 로고
    • Amaryllidaceae and sceletium alkaloids
    • Jin Z (2005) Amaryllidaceae and sceletium alkaloids. Nat Prod Rep 22:111
    • (2005) Nat Prod Rep , vol.22 , pp. 111
    • Jin, Z.1
  • 24
    • 0346433486 scopus 로고    scopus 로고
    • Amaryllidaceae and sceletium alkaloids
    • Jin Z (2003) Amaryllidaceae and sceletium alkaloids. Nat Prod Rep 20:606
    • (2003) Nat Prod Rep , vol.20 , pp. 606
    • Jin, Z.1
  • 25
    • 0035984558 scopus 로고    scopus 로고
    • Amaryllidaceae, sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids
    • Jin Z, Li ZG, Huang RQ (2002) Amaryllidaceae, sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids. Nat Prod Rep 19:454
    • (2002) Nat Prod Rep , vol.19 , pp. 454
    • Jin, Z.1    Li, Z.G.2    Huang, R.Q.3
  • 26
    • 0035138240 scopus 로고    scopus 로고
    • Amaryllidaceae, sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids
    • (and previous reviews in this series)
    • Lewis JR (2001) Amaryllidaceae, sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids. Nat Prod Rep 18:95 (and previous reviews in this series)
    • (2001) Nat Prod Rep , vol.18 , pp. 95
    • Lewis, J.R.1
  • 27
    • 77957118282 scopus 로고
    • Chemical constituents of Amaryllidaceae. Part XIX. The ocurrence of N-(3-hydroxy-4-methoxybenzylidene)-4'-hydroxyphe-nethylamine in Crinum augustum and its biogenetic significance
    • Ghosal S, Kumar Y, Singh SK, Shanthy A (1986) Chemical constituents of Amaryllidaceae. Part XIX. The ocurrence of N-(3-hydroxy-4-methoxybenzylidene)-4'-hydroxyphe-nethylamine in Crinum augustum and its biogenetic significance. J Chem Res (S) 28-29
    • (1986) J Chem Res , vol.S , pp. 28-29
    • Ghosal, S.1    Kumar, Y.2    Singh, S.K.3    Shanthy, A.4
  • 28
    • 0009526828 scopus 로고
    • Isocraugsodine, an N-arylidenephenethylamine from Crinum asiaticum and its E-Z isomerism
    • Ghosal S, Shanthy A, Singh SK (1988) Isocraugsodine, an N-arylidenephenethylamine from Crinum asiaticum and its E-Z isomerism. Phytochemistry 27:1849
    • (1988) Phytochemistry , vol.27 , pp. 1849
    • Ghosal, S.1    Shanthy, A.2    Singh, S.K.3
  • 29
    • 0007633660 scopus 로고
    • Phenol oxidation and biosynthesis. Part VI. The biogenesis of Amaryllidaceae alkaloids
    • Barton DHR, Kirby GW, Taylor JB, Thomas GM (1963) Phenol oxidation and biosynthesis. Part VI. The biogenesis of Amaryllidaceae alkaloids. J Chem Soc 4545-4558
    • (1963) J Chem Soc , pp. 4545-4558
    • Barton, D.1    Kirby, G.W.2    Taylor, J.B.3    Thomas, G.M.4
  • 34
    • 0034685857 scopus 로고    scopus 로고
    • Total synthesis of Amaryllidaceae pyrrolophenan-thridinium alkaloids via the Ziegler-Ullmann reaction: Tortuosine, criasbetaine, and ungeremine
    • Stark LM, Lin XF, Flippin LA (2000) Total synthesis of Amaryllidaceae pyrrolophenan-thridinium alkaloids via the Ziegler-Ullmann reaction: tortuosine, criasbetaine, and ungeremine. J Org Chem 65:3227
    • (2000) J Org Chem , vol.65 , pp. 3227
    • Stark, L.M.1    Lin, X.F.2    Flippin, L.A.3
  • 35
    • 0026570123 scopus 로고
    • Narcissus alkaloids. XVI. (+)-8-O-acetylhomolycorine and vasconine, two novel alkaloids from Narcissus vasconicus
    • Bastida J, Codina C, Viladomat F, Rubiralta M, Quirion JC, Weniger B (1992) Narcissus alkaloids. XVI. (+)-8-O-acetylhomolycorine and vasconine, two novel alkaloids from Narcissus vasconicus. J Nat Prod 55:122
    • (1992) J Nat Prod , vol.55 , pp. 122
    • Bastida, J.1    Codina, C.2    Viladomat, F.3    Rubiralta, M.4    Quirion, J.C.5    Weniger, B.6
  • 38
    • 0037562732 scopus 로고    scopus 로고
    • The genus Galanthus
    • Mathew B (ed),. Timber Press, Oregon
    • Davis AP (1999) The genus Galanthus. In: Mathew B (ed) A Botanical magazine monograph. Timber Press, Oregon
    • (1999) A Botanical Magazine Monograph
    • Davis, A.P.1
  • 40
    • 0033005444 scopus 로고    scopus 로고
    • Three new tazettine-type alkaloids from Galanthus gracilis and Galanthus plicatus subsp. Byzantinus
    • Unver N, Noyan S, Gozler T, Onur MA, Gozler B, Hesse M (1999) Three new tazettine-type alkaloids from Galanthus gracilis and Galanthus plicatus subsp. byzantinus. Planta Med 65:347
    • (1999) Planta Med , vol.65 , pp. 347
    • Unver, N.1    Noyan, S.2    Gozler, T.3    Onur, M.A.4    Gozler, B.5    Hesse, M.6
  • 41
    • 0035307150 scopus 로고    scopus 로고
    • Four new Amaryllidaceae alkaloids from Galanthus gracilis and Galanthus plicatus subsp. Byzantinus
    • Unver N, Noyan S, Gozler B, Gozler T, Werner C, Hesse M (2001) Four new Amaryllidaceae alkaloids from Galanthus gracilis and Galanthus plicatus subsp. byzantinus. Heterocycles 55:641
    • (2001) Heterocycles , vol.55 , pp. 641
    • Unver, N.1    Noyan, S.2    Gozler, B.3    Gozler, T.4    Werner, C.5    Hesse, M.6
  • 43
    • 0345280011 scopus 로고    scopus 로고
    • Two novel dinitrogenous alkaloids from Galanthus plicatus subsp. Byzantinus (Amaryllidaceae)
    • Unver N, Gozler T, Walch N, Gozler B, Hesse M (1999) Two novel dinitrogenous alkaloids from Galanthus plicatus subsp. byzantinus (Amaryllidaceae). Phytochemistry 50:1255
    • (1999) Phytochemistry , vol.50 , pp. 1255
    • Unver, N.1    Gozler, T.2    Walch, N.3    Gozler, B.4    Hesse, M.5
  • 45
    • 73649089300 scopus 로고    scopus 로고
    • Glycosides of benzodioxole-indole alkaloids from Narcissus having axial chirality
    • Rezanka T, Rezanka P, Sigler K (2010) Glycosides of benzodioxole-indole alkaloids from Narcissus having axial chirality. Phytochemistry 71:301
    • (2010) Phytochemistry , vol.71 , pp. 301
    • Rezanka, T.1    Rezanka, P.2    Sigler, K.3
  • 47
    • 32644441114 scopus 로고    scopus 로고
    • An unusual pentacyclic dinitrogenous alkaloid from Galanthus gracilis
    • Unver N, Kaya GI (2005) An unusual pentacyclic dinitrogenous alkaloid from Galanthus gracilis. Turk J Chem 29:547
    • (2005) Turk J Chem , vol.29 , pp. 547
    • Unver, N.1    Kaya, G.I.2
  • 52
    • 66949112200 scopus 로고    scopus 로고
    • Two new Amaryllidaceae alkaloids from the bulbs of Lycoris radiate
    • Wang L, Zhang X, Yin Z, Wang Y, Ye W (2009) Two new Amaryllidaceae alkaloids from the bulbs of Lycoris radiate. Chem Pharm Bull 57:610
    • (2009) Chem Pharm Bull , vol.57 , pp. 610
    • Wang, L.1    Zhang, X.2    Yin, Z.3    Wang, Y.4    Ye, W.5
  • 54
    • 70350286039 scopus 로고    scopus 로고
    • Chemical constituents of Crinum asiaticum L. Var sinicum Baker and their cytotoxic activities
    • Sun Q, Shen Y, Tian J, Tang J, Su J, Liu R, Li H, Xu X, Zhang W (2009) Chemical constituents of Crinum asiaticum L. var sinicum Baker and their cytotoxic activities. Chem Biodivers 6:1751
    • (2009) Chem Biodivers , vol.6 , pp. 1751
    • Sun, Q.1    Shen, Y.2    Tian, J.3    Tang, J.4    Su, J.5    Liu, R.6    Li, H.7    Xu, X.8    Zhang, W.9
  • 58
    • 10344249416 scopus 로고    scopus 로고
    • Search for bioactive alkaloids in Hymenocallis species
    • Rivero N, Gomez M, Medina JD (2004) Search for bioactive alkaloids in Hymenocallis species. Pharm Biol 42:280
    • (2004) Pharm Biol , vol.42 , pp. 280
    • Rivero, N.1    Gomez, M.2    Medina, J.D.3
  • 63
    • 0034090008 scopus 로고    scopus 로고
    • Alkaloids and triterpenoids from Ammocharis coranica (Amaryllidaceae)
    • Koorbanally N, Mulholland DA, Crouch N (2000) Alkaloids and triterpenoids from Ammocharis coranica (Amaryllidaceae). Phytochemistry 54:93
    • (2000) Phytochemistry , vol.54 , pp. 93
    • Koorbanally, N.1    Mulholland, D.A.2    Crouch, N.3
  • 64
    • 73949134530 scopus 로고    scopus 로고
    • Quantitative determination of Amaryllidaceae alkaloids from Galanthus reginae-olgae subsp. Vernalis and in vitro activities relevant for neurodegenerative diseases
    • Conforti F, Loizzo MR, Marrelli M, Menichini F, Statti GA, Uzunov D, Menichini F (2010) Quantitative determination of Amaryllidaceae alkaloids from Galanthus reginae-olgae subsp. vernalis and in vitro activities relevant for neurodegenerative diseases. Pharm Biol 48:2
    • (2010) Pharm Biol , vol.48 , pp. 2
    • Conforti, F.1    Loizzo, M.R.2    Marrelli, M.3    Menichini, F.4    Statti, G.A.5    Uzunov, D.6    Menichini, F.7
  • 66
    • 15444366595 scopus 로고    scopus 로고
    • Alkaloid and phenolic compounds of Galanthus caucasicus, Magnolia obovata, Cocculus laurifolius, and Veratrum lobelianum grown in Georgia
    • Tsakadze DM, Samsoniya SA, Ziaev R, Abdusamatov A (2005) Alkaloid and phenolic compounds of Galanthus caucasicus, Magnolia obovata, Cocculus laurifolius, and Veratrum lobelianum grown in Georgia. Mol Divers 9:41
    • (2005) Mol Divers , vol.9 , pp. 41
    • Tsakadze, D.M.1    Samsoniya, S.A.2    Ziaev, R.3    Abdusamatov, A.4
  • 68
    • 84881432379 scopus 로고    scopus 로고
    • Highly efficient, sensitive and selective molecular screening of acetylcholinesterase inhibitors of natural origin by SPE-LC/ESI-TOF-MS and novel TLC-based bioauthography
    • Mroczek T, Glowniak K (2009) Highly efficient, sensitive and selective molecular screening of acetylcholinesterase inhibitors of natural origin by SPE-LC/ESI-TOF-MS and novel TLC-based bioauthography. Planta Med 75: SL64
    • (2009) Planta Med , vol.75
    • Mroczek, T.1    Glowniak, K.2
  • 70
    • 17444427134 scopus 로고    scopus 로고
    • Alkaloids from three ethnomedicinal Haemanthus species: H. Albiflos, H. Deformis and H. Pauculifolius (Amaryllidaceae)
    • Crouch NR, Pohl TL, Mulholland DA, Ndlovu E (2005) Alkaloids from three ethnomedicinal Haemanthus species: H. albiflos, H. deformis and H. pauculifolius (Amaryllidaceae). S Afr J Bot 71:49
    • (2005) S Afr J Bot , vol.71 , pp. 49
    • Crouch, N.R.1    Pohl, T.L.2    Mulholland, D.A.3    Ndlovu, E.4
  • 77
    • 70349661827 scopus 로고    scopus 로고
    • Chemical constituents of the bulbs of Habranthus brachyandrus and their cytotoxic activities
    • Jitsuno M, Yokosuka A, Sakagami H, Mimaki Y (2009) Chemical constituents of the bulbs of Habranthus brachyandrus and their cytotoxic activities. Chem Pharm Bull 57:1153
    • (2009) Chem Pharm Bull , vol.57 , pp. 1153
    • Jitsuno, M.1    Yokosuka, A.2    Sakagami, H.3    Mimaki, Y.4
  • 78
    • 76949108840 scopus 로고    scopus 로고
    • Isolation of acetylcholinesterase inhibitory alkaloids from Nerine bowdenii
    • van Rijn RM, Rhee IK, Verpoorte R (2010) Isolation of acetylcholinesterase inhibitory alkaloids from Nerine bowdenii. Nat Prod Res 24:222
    • (2010) Nat Prod Res , vol.24 , pp. 222
    • Van Rijn, R.M.1    Rhee, I.K.2    Verpoorte, R.3
  • 82
    • 61449130476 scopus 로고    scopus 로고
    • Alkaloidal Constituents of Pancratium tortuosum
    • Toaima SM (2007) Alkaloidal Constituents of Pancratium tortuosum. Alexandria J Pharm Sci 21:63
    • (2007) Alexandria J Pharm Sci , vol.21 , pp. 63
    • Toaima, S.M.1
  • 83
    • 3242758865 scopus 로고    scopus 로고
    • New crinine-type alkaloids with inhibitory effect on induction of inducible nitric oxide synthase from Crinum yemense
    • Abdel-Halim OB, Morikawa T, Ando S, Matsuda H, Yoshikawa M (2004) New crinine-type alkaloids with inhibitory effect on induction of inducible nitric oxide synthase from Crinum yemense. J Nat Prod 67:1119
    • (2004) J Nat Prod , vol.67 , pp. 1119
    • Abdel-Halim, O.B.1    Morikawa, T.2    Ando, S.3    Matsuda, H.4    Yoshikawa, M.5
  • 88
    • 22644443386 scopus 로고    scopus 로고
    • A new alkaloid from Narcissus serotinus L
    • Vrondeli A, Kefalas P, Kokkalou E (2005) A new alkaloid from Narcissus serotinus L. Pharmazie 60:559
    • (2005) Pharmazie , vol.60 , pp. 559
    • Vrondeli, A.1    Kefalas, P.2    Kokkalou, E.3
  • 90
    • 0036277049 scopus 로고    scopus 로고
    • Antiproliferative amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis
    • Hohmann J, Forgo P, Molnar J, Wolfard K, Molnar A, Thalhammer T, Mathe I, Sharples D (2002) Antiproliferative amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis. Planta Med 68:454
    • (2002) Planta Med , vol.68 , pp. 454
    • Hohmann, J.1    Forgo, P.2    Molnar, J.3    Wolfard, K.4    Molnar, A.5    Thalhammer, T.6    Mathe, I.7    Sharples, D.8
  • 91
    • 84879936738 scopus 로고    scopus 로고
    • Sustainable use of various Amaryllidaceae plants against Alzheimer’s disease
    • Ilkay O, Bilge S (2005) Sustainable use of various Amaryllidaceae plants against Alzheimer’s disease. Acta Hortic 678:59
    • (2005) Acta Hortic , vol.678 , pp. 59
    • Ilkay, O.1    Bilge, S.2
  • 94
    • 0242320486 scopus 로고    scopus 로고
    • Galanthindole: A new indole alkaloid from Galanthus plicatus ssp. Byzantinus
    • Unver N, Kaya GI, Werner C, Verpoorte R, Gozler B (2003) Galanthindole: A new indole alkaloid from Galanthus plicatus ssp. byzantinus. Planta Med 69:869
    • (2003) Planta Med , vol.69 , pp. 869
    • Unver, N.1    Kaya, G.I.2    Werner, C.3    Verpoorte, R.4    Gozler, B.5
  • 96
    • 41249090622 scopus 로고    scopus 로고
    • N-Alkylated galanthamine derivatives: Potent acetylcholinesterase inhibitors from Leucojum aestivum
    • Berkov S, Codina C, Viladomat F, Bastida J (2008) N-Alkylated galanthamine derivatives: potent acetylcholinesterase inhibitors from Leucojum aestivum. Bioorg Med Chem Lett 18:2263
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 2263
    • Berkov, S.1    Codina, C.2    Viladomat, F.3    Bastida, J.4
  • 97
    • 29044443862 scopus 로고    scopus 로고
    • Leucovernine and acetylleucovernine, alkaloids from Leucojum vernum
    • Forgo P, Hohmann J (2005) Leucovernine and acetylleucovernine, alkaloids from Leucojum vernum. J Nat Prod 68:1588
    • (2005) J Nat Prod , vol.68 , pp. 1588
    • Forgo, P.1    Hohmann, J.2
  • 99
    • 14544298394 scopus 로고    scopus 로고
    • Antineoplastic agents. 527. Synthesis of 7-deoxynarcistatin, 7-deoxy-trans-dihydronarcistatin, and trans-dihydronarcistatin 1(1)
    • Pettit GR, Melody N (2005) Antineoplastic agents. 527. Synthesis of 7-deoxynarcistatin, 7-deoxy-trans-dihydronarcistatin, and trans-dihydronarcistatin 1(1). J Nat Prod 68:207
    • (2005) J Nat Prod , vol.68 , pp. 207
    • Pettit, G.R.1    Melody, N.2
  • 100
    • 24744462677 scopus 로고    scopus 로고
    • Antineoplastic agents. 553. The Texas grasshopper Brachystola magna
    • Pettit GR, Meng Y, Herald DL, Knight JC, Day JF (2005) Antineoplastic agents. 553. The Texas grasshopper Brachystola magna. J Nat Prod 68:1256
    • (2005) J Nat Prod , vol.68 , pp. 1256
    • Pettit, G.R.1    Meng, Y.2    Herald, D.L.3    Knight, J.C.4    Day, J.F.5
  • 101
    • 0036915966 scopus 로고    scopus 로고
    • A new phenanthridine alkaloid from Hymenocallis festalis
    • Hohmann J, Forgo P, Szabo P (2002) A new phenanthridine alkaloid from Hymenocallis festalis. Fitoterapia 73:749
    • (2002) Fitoterapia , vol.73 , pp. 749
    • Hohmann, J.1    Forgo, P.2    Szabo, P.3
  • 105
    • 37049041839 scopus 로고
    • Alkaloid biosynthesis. Part III. Amaryllidaceae alkaloids: The biosynthesis of lycorine and its relatives
    • Battersby AR, Binks R, Breuer SW, Fales HM, Wildman WC, Highet RJ (1964) Alkaloid biosynthesis. Part III. Amaryllidaceae alkaloids: the biosynthesis of lycorine and its relatives. J Chem Soc 1595-1609
    • (1964) J Chem Soc , pp. 1595-1609
    • Battersby, A.R.1    Binks, R.2    Breuer, S.W.3    Fales, H.M.4    Wildman, W.C.5    Highet, R.J.6
  • 106
    • 37049136463 scopus 로고
    • Phenol oxidation and biosynthesis. Part IX. The biosynthesis of norpluviine and galanthine
    • Kirby GW, Tiwari HP (1966) Phenol oxidation and biosynthesis. Part IX. The biosynthesis of norpluviine and galanthine. J Chem Soc (C) 676-682
    • (1966) J Chem Soc (C) , pp. 676-682
    • Kirby, G.W.1    Tiwari, H.P.2
  • 107
    • 37049125476 scopus 로고
    • Biosynthetic incorporation of [β-14C, 3,5-2H2, 4-3H]-cinnamic acid into capsaicin and norpluviine: Lack of an apparent isotope effect following an NIH shift
    • 3H]-cinnamic acid into capsaicin and norpluviine: lack of an apparent isotope effect following an NIH shift. J Chem Soc Chem Commun 1075-1077
    • (1969) J Chem Soc Chem Commun , pp. 1075-1077
    • Bowman, W.R.1    Bruce, I.T.2    Kirby, G.W.3
  • 108
    • 0014218759 scopus 로고
    • Alkaloid biosynthesis and interconversions. The conversion of caranine to lycorine
    • Wildman WC, Heimer NE (1967) Alkaloid biosynthesis and interconversions. The conversion of caranine to lycorine. J Am Chem Soc 89:5265
    • (1967) J am Chem Soc , vol.89 , pp. 5265
    • Wildman, W.C.1    Heimer, N.E.2
  • 109
    • 37049116561 scopus 로고
    • Stereochemistry of protonation and hydroxylation in the biosynthesis of norpluviine and lycorine
    • Bruce IT, Kirby GW (1968) Stereochemistry of protonation and hydroxylation in the biosynthesis of norpluviine and lycorine. J Chem Soc Chem Commun 207-208
    • (1968) J Chem Soc Chem Commun , pp. 207-208
    • Bruce, I.T.1    Kirby, G.W.2
  • 110
    • 37049129601 scopus 로고
    • Stereochemistry of hydroxylation in the biosynthesis of lycorine in Clivia miniata Regel
    • Fuganti C, Mazza M (1972) Stereochemistry of hydroxylation in the biosynthesis of lycorine in Clivia miniata Regel. J Chem Soc Chem Commun 936-937
    • (1972) J Chem Soc Chem Commun , pp. 936-937
    • Fuganti, C.1    Mazza, M.2
  • 112
  • 113
    • 77950817924 scopus 로고    scopus 로고
    • Total synthesis of the lycorenine-type amaryllidaceae alkaloid (+/-)-clivonine via a biomimetic ring-switch from a lycorine-type progenitor
    • Manas CG, Paddock VL, Bochet CG, Spivey AC, White AJP, Mann I, Oppolzer W (2010) Total synthesis of the lycorenine-type amaryllidaceae alkaloid (+/-)-clivonine via a biomimetic ring-switch from a lycorine-type progenitor. J Am Chem Soc 132:5176
    • (2010) J am Chem Soc , vol.132 , pp. 5176
    • Manas, C.G.1    Paddock, V.L.2    Bochet, C.G.3    Spivey, A.C.4    White, A.5    Mann, I.6    Oppolzer, W.7
  • 115
    • 33749413047 scopus 로고
    • Biosynthetic oxidation and rearrangement of vittatine and its derivatives
    • Feinstein AI, Wildman WC (1976) Biosynthetic oxidation and rearrangement of vittatine and its derivatives. J Org Chem 41:2447
    • (1976) J Org Chem , vol.41 , pp. 2447
    • Feinstein, A.I.1    Wildman, W.C.2
  • 116
    • 25444489908 scopus 로고
    • Biological interconversions in the Amaryllidaceae. I. The haemanthamine-haemanthidine-Tazettine sequence
    • Fales HM, Wildman WC (1964) Biological interconversions in the Amaryllidaceae. I. The haemanthamine-haemanthidine-Tazettine sequence. J Am Chem Soc 86:294
    • (1964) J am Chem Soc , vol.86 , pp. 294
    • Fales, H.M.1    Wildman, W.C.2
  • 117
    • 37049122634 scopus 로고
    • Late intermediates in the biosynthesis of narciclasine
    • Fuganti C, Mazza M (1971) Late intermediates in the biosynthesis of narciclasine. J Chem Soc Chem Commun 1388-1389
    • (1971) J Chem Soc Chem Commun , pp. 1388-1389
    • Fuganti, C.1    Mazza, M.2
  • 118
    • 37049129359 scopus 로고
    • The absolute configuration of narciclasine: A biosynthetic approach
    • Fuganti C, Mazza M (1972) The absolute configuration of narciclasine: A biosynthetic approach. J Chem Soc Chem Commun 239-239
    • (1972) J Chem Soc Chem Commun , pp. 239
    • Fuganti, C.1    Mazza, M.2
  • 119
    • 37049136921 scopus 로고
    • The biosynthesis of the alkaloid ismine
    • Fuganti C, Mazza M (1970) The biosynthesis of the alkaloid ismine. J Chem Soc Chem Commun 1466-1467
    • (1970) J Chem Soc Chem Commun , pp. 1466-1467
    • Fuganti, C.1    Mazza, M.2
  • 120
    • 0344681654 scopus 로고
    • Biosynthesis of galanthamine: Feeding experiments in Leucojum aestivum (Amaryllidaceae)
    • Fuganti C (1969) Biosynthesis of galanthamine: feeding experiments in Leucojum aestivum (Amaryllidaceae). La Chimica e l’Industria 51:1254
    • (1969) La Chimica E l’Industria , vol.51 , pp. 1254
    • Fuganti, C.1
  • 122
    • 0031694246 scopus 로고    scopus 로고
    • Biosynthesis of the Amaryllidaceae alkaloid galanthamine
    • Eichhorn J, Takada T, Kita Y, Zenk MH (1998) Biosynthesis of the Amaryllidaceae alkaloid galanthamine. Phytochemistry 49:1037
    • (1998) Phytochemistry , vol.49 , pp. 1037
    • Eichhorn, J.1    Takada, T.2    Kita, Y.3    Zenk, M.H.4
  • 123
    • 4444357067 scopus 로고    scopus 로고
    • Quinone methide initiated cyclization reaction: Synthesis of 4-aryl-1,2,3,4-tetrahydroisoquinolines
    • Raju BC, Neelakantan P, Bhalerao UT (2004) Quinone methide initiated cyclization reaction: synthesis of 4-aryl-1,2,3,4-tetrahydroisoquinolines. Tetrahedron Lett 45:7487
    • (2004) Tetrahedron Lett , vol.45 , pp. 7487
    • Raju, B.C.1    Neelakantan, P.2    Bhalerao, U.T.3
  • 124
    • 67651155818 scopus 로고    scopus 로고
    • Anticancer evaluation of structurally diverse Amaryllidaceae alkaloids and their synthetic derivatives
    • Evidente A, Kornienko A (2009) Anticancer evaluation of structurally diverse Amaryllidaceae alkaloids and their synthetic derivatives. Phytochem Rev 8:449
    • (2009) Phytochem Rev , vol.8 , pp. 449
    • Evidente, A.1    Kornienko, A.2
  • 126
    • 67651157036 scopus 로고    scopus 로고
    • Biological evaluation of structurally diverse Amaryllidaceae alkaloids and their synthetic derivatives: Discovery of novel leads for anticancer drug design
    • Evidente A, Kireev AS, Jenkins AR, Romero AE, Steelant WFA, van Stambrouck S, Kornienko A (2009) Biological evaluation of structurally diverse Amaryllidaceae alkaloids and their synthetic derivatives: discovery of novel leads for anticancer drug design. Planta Med 75:501
    • (2009) Planta Med , vol.75 , pp. 501
    • Evidente, A.1    Kireev, A.S.2    Jenkins, A.R.3    Romero, A.E.4    Steelant, W.5    Van Stambrouck, S.6    Kornienko, A.7
  • 127
  • 128
    • 57749088585 scopus 로고    scopus 로고
    • Lycorine induces apoptosis and down-regulation of Mcl-1 in human leukemia cells
    • Liu X, Jiang J, Jiao X, Wu Y, Lin J, Cai Y (2009) Lycorine induces apoptosis and down-regulation of Mcl-1 in human leukemia cells. Cancer Lett 274:16
    • (2009) Cancer Lett , vol.274 , pp. 16
    • Liu, X.1    Jiang, J.2    Jiao, X.3    Wu, Y.4    Lin, J.5    Cai, Y.6
  • 129
    • 67249134952 scopus 로고    scopus 로고
    • Structure-activity studies on the lycorine pharmacophore: A potent inducer of apoptosis in human leukemia cells
    • McNulty J, Nair JJ, Bastida J, Pandey S, Griffin C (2009) Structure-activity studies on the lycorine pharmacophore: A potent inducer of apoptosis in human leukemia cells. Phytochemistry 70:913
    • (2009) Phytochemistry , vol.70 , pp. 913
    • Mc Nulty, J.1    Nair, J.J.2    Bastida, J.3    Pandey, S.4    Griffin, C.5
  • 130
    • 10044221979 scopus 로고    scopus 로고
    • Effects of lycorine on HL-60 cells via arresting cell cycle and inducing apoptosis
    • Liu J, Hu W, He L, Ye M, Li Y (2004) Effects of lycorine on HL-60 cells via arresting cell cycle and inducing apoptosis. FEBS Lett 578:245
    • (2004) FEBS Lett , vol.578 , pp. 245
    • Liu, J.1    Hu, W.2    He, L.3    Ye, M.4    Li, Y.5
  • 131
    • 70350068068 scopus 로고    scopus 로고
    • Lycorine, the main phenanthridine Amaryllidaceae alkaloid, exhibits significant antitumor activity in cancer cells that display resistance to proapoptotic stimuli: An investigation of structure-activity relationship and mechanistic insight
    • Lamoral-theys D, Andolfi A, van Goietsenoven G, Cimmino A, Le Calve B, Wauthoz N, Magalizzi V, Gras T, Bruyere C, Dubois J, Mathieu V, Kornienko A, Kiss R, Evidente A (2009) Lycorine, the main phenanthridine Amaryllidaceae alkaloid, exhibits significant antitumor activity in cancer cells that display resistance to proapoptotic stimuli: an investigation of structure-activity relationship and mechanistic insight. J Med Chem 52:6244
    • (2009) J Med Chem , vol.52 , pp. 6244
    • Lamoral-Theys, D.1    Olfi, A.2    Van Goietsenoven, G.3    Cimmino, A.4    Le Calve, B.5    Wauthoz, N.6    Magalizzi, V.7    Gras, T.8    Bruyere, C.9    Dubois, J.10    Mathieu, V.11    Kornienko, A.12    Kiss, R.13    Evidente, A.14
  • 133
    • 58649100667 scopus 로고    scopus 로고
    • A single-amino acid substitution in West Nile virus 2 K peptide between NS4A and NS4B confers resistance to lycorine, a flavivirus inhibitor
    • Zou G, Puig-Basagoiti F, Zhang B, Qing M, Chen L, Pankiewicz KW, Felczak K, Yuan Z, Shi P (2009) A single-amino acid substitution in West Nile virus 2 K peptide between NS4A and NS4B confers resistance to lycorine, a flavivirus inhibitor. Virology 384:242
    • (2009) Virology , vol.384 , pp. 242
    • Zou, G.1    Puig-Basagoiti, F.2    Zhang, B.3    Qing, M.4    Chen, L.5    Pankiewicz, K.W.6    Felczak, K.7    Yuan, Z.8    Shi, P.9
  • 135
    • 56049117205 scopus 로고    scopus 로고
    • Anti-inflammatory activity of Crinum asiaticum Linne var. Japonicum extract and its application as a cosmeceutical ingredient
    • Kim YH, Kim KH, Han CS, Park SH, Yang HC, Lee BY, Eom S, Kim Y, Kim J, Lee NH (2008) Anti-inflammatory activity of Crinum asiaticum Linne var. japonicum extract and its application as a cosmeceutical ingredient. J Cosmet Sci 59:419
    • (2008) J Cosmet Sci , vol.59 , pp. 419
    • Kim, Y.H.1    Kim, K.H.2    Han, C.S.3    Park, S.H.4    Yang, H.C.5    Lee, B.Y.6    Eom, S.7    Kim, Y.8    Kim, J.9    Lee, N.H.10
  • 136
    • 34547155684 scopus 로고    scopus 로고
    • Activity of lycorine extracted from Pancratium maritimum on growth of same yeast strains
    • De Laurentis N, Rosato A, Vitali C, Leone L, Milillo MA (2004) Activity of lycorine extracted from Pancratium maritimum on growth of same yeast strains. Riv Ital EPPOS 38:19
    • (2004) Riv Ital EPPOS , vol.38 , pp. 19
    • De Laurentis, N.1    Rosato, A.2    Vitali, C.3    Leone, L.4    Milillo, M.A.5
  • 137
    • 0347987011 scopus 로고    scopus 로고
    • Antimalarial activity screening of some alkaloids and the plant extracts from Amaryllidaceae
    • Sener B, Orhan I, Satayavivad J (2003) Antimalarial activity screening of some alkaloids and the plant extracts from Amaryllidaceae. PhytotherRes 17:1220
    • (2003) Phytotherres , vol.17 , pp. 1220
    • Sener, B.1    Orhan, I.2    Satayavivad, J.3
  • 138
    • 14344253534 scopus 로고    scopus 로고
    • Choline esterase inhibitory properties of alkaloids from two Nigerian Crinum species
    • Houghton PJ, Agbedahunsi JM, Adegbulugbe A (2004) Choline esterase inhibitory properties of alkaloids from two Nigerian Crinum species. Phytochemistry 65:2893
    • (2004) Phytochemistry , vol.65 , pp. 2893
    • Houghton, P.J.1    Agbedahunsi, J.M.2    Adegbulugbe, A.3
  • 139
    • 5444233550 scopus 로고    scopus 로고
    • Alkaloids from Leucojum vernum and antiretroviral activity of Amaryllidaceae alkaloids
    • Szlavik L, Gyuris A, Minarovits J, Forgo P, Molnar J, Hohmann J (2004) Alkaloids from Leucojum vernum and antiretroviral activity of Amaryllidaceae alkaloids. Planta Med 70:871
    • (2004) Planta Med , vol.70 , pp. 871
    • Szlavik, L.1    Gyuris, A.2    Minarovits, J.3    Forgo, P.4    Molnar, J.5    Hohmann, J.6
  • 140
    • 33645997535 scopus 로고    scopus 로고
    • Investigation of antimicrobial and cytotoxic properties of alkaloids from some species of Crinum in Vietnam
    • Phan TS, Tran DB, Phan GM, Nguye TM, Hoang TH, Le HM (2003) Investigation of antimicrobial and cytotoxic properties of alkaloids from some species of Crinum in Vietnam. Tap Chi Duoc Hoc 18-21
    • (2003) Tap Chi Duoc Hoc , pp. 18-21
    • Phan, T.S.1    Tran, D.B.2    Phan, G.M.3    Nguye, T.M.4    Hoang, T.H.5    Le, H.M.6
  • 141
  • 142
    • 1842431888 scopus 로고    scopus 로고
    • Acetylcholinesterase enzyme inhibitory effects of Amaryllidaceae alkaloids
    • Elgorashi EE, Stafford GI, van Staden J (2004) Acetylcholinesterase enzyme inhibitory effects of Amaryllidaceae alkaloids. Planta Med 70:260
    • (2004) Planta Med , vol.70 , pp. 260
    • Elgorashi, E.E.1    Stafford, G.I.2    Van Staden, J.3
  • 143
    • 22044455873 scopus 로고    scopus 로고
    • Isolation of the acetylcholinesterase inhibitor ungeremine from Nerine bowdenii by preparative HPLC coupled on-line to a flow assay system
    • Rhee K, Appels N, Hofte B, Karabatak B, Erkelens C, Stark LM, Flippin LA, Verpoorte R (2004) Isolation of the acetylcholinesterase inhibitor ungeremine from Nerine bowdenii by preparative HPLC coupled on-line to a flow assay system. Biol Pharm Bull 27:1804
    • (2004) Biol Pharm Bull , vol.27 , pp. 1804
    • Rhee, K.1    Appels, N.2    Hofte, B.3    Karabatak, B.4    Erkelens, C.5    Stark, L.M.6    Flippin, L.A.7    Verpoorte, R.8
  • 147
    • 0024602642 scopus 로고
    • Effect of alkaloids isolated from Amaryllidaceae on herpes simplex virus
    • Renard-Nozaki J, Kim T, Imakura Y, Kihara M, Kobayashi S (1989) Effect of alkaloids isolated from Amaryllidaceae on herpes simplex virus. Res Virol 140:115
    • (1989) Res Virol , vol.140 , pp. 115
    • Renard-Nozaki, J.1    Kim, T.2    Imakura, Y.3    Kihara, M.4    Kobayashi, S.5
  • 149
    • 84881428187 scopus 로고    scopus 로고
    • High-performance countercurrent chromatography for the efficient isolation of alkaloid acetylcholinesterase inhibitors from Nerine species (Amaryllidaceae)
    • Marston A, Cawood M, van der Westhuizen J, Zietsman P (2010) High-performance countercurrent chromatography for the efficient isolation of alkaloid acetylcholinesterase inhibitors from Nerine species (Amaryllidaceae). Planta Med 76:P061
    • (2010) Planta Med , vol.76
    • Marston, A.1    Cawood, M.2    Van Der Westhuizen, J.3    Zietsman, P.4
  • 150
    • 65749095009 scopus 로고    scopus 로고
    • Structure activity studies on the crinane alkaloid apoptosis-inducing pharmacophore
    • McNulty J, Nair JJ, Bastida J, Pandey S, Griffin C (2009) Structure activity studies on the crinane alkaloid apoptosis-inducing pharmacophore. Nat Prod Commun 4:483
    • (2009) Nat Prod Commun , vol.4 , pp. 483
    • Mc Nulty, J.1    Nair, J.J.2    Bastida, J.3    Pandey, S.4    Griffin, C.5
  • 152
    • 34250849599 scopus 로고    scopus 로고
    • Selective cytotoxicity of pancratistatin-related natural Amaryllidaceae alkaloids: Evaluation of the activity of two new compounds
    • Griffin C, Sharda N, Sood D, Nair J, McNulty J, Pandey S (2007) Selective cytotoxicity of pancratistatin-related natural Amaryllidaceae alkaloids: evaluation of the activity of two new compounds. Cancer Cell Int 7:10
    • (2007) Cancer Cell Int , vol.7 , pp. 10
    • Griffin, C.1    Sharda, N.2    Sood, D.3    Nair, J.4    Mc Nulty, J.5    Pandey, S.6
  • 153
    • 33645985839 scopus 로고    scopus 로고
    • Inhibition of [3 H]citalopram binding to the rat brain serotonin transporter by Amaryllidaceae alkaloids
    • Elgorashi EE, Stafford GI, Jager AK, van Staden J (2006) Inhibition of [3 H]citalopram binding to the rat brain serotonin transporter by Amaryllidaceae alkaloids. Planta Med 72:470
    • (2006) Planta Med , vol.72 , pp. 470
    • Elgorashi, E.E.1    Stafford, G.I.2    Jager, A.K.3    Van Staden, J.4
  • 156
    • 34347250495 scopus 로고    scopus 로고
    • In vitro evaluation of the antiinflammatory, antioxidant and antimicrobial activities of the montanine alkaloid
    • Castilhos TS, Giordani RB, Henriques AT, Menezes FS, Zuanazzi JAS (2007) In vitro evaluation of the antiinflammatory, antioxidant and antimicrobial activities of the montanine alkaloid. Rev Bras Farm 17:209
    • (2007) Rev Bras Farm , vol.17 , pp. 209
    • Castilhos, T.S.1    Giordani, R.B.2    Henriques, A.T.3    Menezes, F.S.4    Zuanazzi, J.5
  • 163
    • 34948883332 scopus 로고    scopus 로고
    • The Amaryllidaceae isocarbostyril narciclasine induces apoptosis by activation of the death receptor and/or mitochondrial pathways in cancer cells but not in normal fibroblasts
    • Dumont P, Ingrassia L, Rouzeau S, Ribaucour F, Thomas S, Roland I, Darro F, Lefranc F, Kiss R (2007) The Amaryllidaceae isocarbostyril narciclasine induces apoptosis by activation of the death receptor and/or mitochondrial pathways in cancer cells but not in normal fibroblasts. Neoplasia 9:766
    • (2007) Neoplasia , vol.9 , pp. 766
    • Dumont, P.1    Ingrassia, L.2    Rouzeau, S.3    Ribaucour, F.4    Thomas, S.5    Roland, I.6    Darro, F.7    Lefranc, F.8    Kiss, R.9
  • 164
    • 34547149015 scopus 로고    scopus 로고
    • Effects of narciclasine on cells of callus of wheat and tobacco
    • Wan Y, Bi Y, Liu Z (2004) Effects of narciclasine on cells of callus of wheat and tobacco. Shanghai Daxue Xuebao Ziran Kexueban 10:493
    • (2004) Shanghai Daxue Xuebao Ziran Kexueban , vol.10 , pp. 493
    • Wan, Y.1    Bi, Y.2    Liu, Z.3
  • 165
    • 1542327282 scopus 로고    scopus 로고
    • Daffodil flowers delay senescence in cut Iris flowers
    • van Doorn WG, Sinz A, Tomassen MM (2004) Daffodil flowers delay senescence in cut Iris flowers. Phytochemistry 65:571
    • (2004) Phytochemistry , vol.65 , pp. 571
    • Van Doorn, W.G.1    Sinz, A.2    Tomassen, M.M.3
  • 166
    • 21244484687 scopus 로고    scopus 로고
    • Pancratistatin: A natural anti-cancer compound that targets mitochondria specifically in cancer cells to induce apoptosis
    • Mclachlan A, Kekre N, McNulty J, Pandey S (2005) Pancratistatin: a natural anti-cancer compound that targets mitochondria specifically in cancer cells to induce apoptosis. Apoptosis 10:619
    • (2005) Apoptosis , vol.10 , pp. 619
    • Mc Lachlan, A.1    Kekre, N.2    Mc Nulty, J.3    Pandey, S.4
  • 167
    • 21244439798 scopus 로고    scopus 로고
    • Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells
    • Kekre N, Griffin C, McNulty J, Pandey S (2005) Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells. Cancer Chemother Pharmacol 56:29
    • (2005) Cancer Chemother Pharmacol , vol.56 , pp. 29
    • Kekre, N.1    Griffin, C.2    Mc Nulty, J.3    Pandey, S.4
  • 168
    • 33645450644 scopus 로고    scopus 로고
    • Acetylcholinesterase inhibitors from plants and fungi
    • Houghton PJ, Ren Y, Howes M (2006) Acetylcholinesterase inhibitors from plants and fungi. Nat Prod Rep 23:181
    • (2006) Nat Prod Rep , vol.23 , pp. 181
    • Houghton, P.J.1    Ren, Y.2    Howes, M.3
  • 169
    • 14544298394 scopus 로고    scopus 로고
    • Antineoplastic agents. 527. Synthesis of 7-deoxynarcistatin, 7-deoxy-trans-dihydronarcistatin, and trans-dihydronarcistatin 1(1)
    • Pettit GR, Melody N (2005) Antineoplastic agents. 527. Synthesis of 7-deoxynarcistatin, 7-deoxy-trans-dihydronarcistatin, and trans-dihydronarcistatin 1(1). J Nat Prod 68:207
    • (2005) J Nat Prod , vol.68 , pp. 207
    • Pettit, G.R.1    Melody, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.