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Volumn 9, Issue 4, 2011, Pages 259-263

Cytotoxic Indole Alkaloids from Melodinus fusiformis and M. morsei

Author keywords

Bisindole alkaloids; Cytotoxicity; M. morsei; Melodinus fusiformi; Melofusine I; Melomorsine I

Indexed keywords

10 HYDROXYSCANDINE; 11 HYDROXY 14,15 EPOXYTABERSONINE; 11 HYDROXY 19 ACETYL TABERSONINE; 11 HYDROXYTABERSONINE; 11 HYDROXYVINCADIFFORMINE; 19 ACETYLTABERSONINE; 19 EPI MELOSCANDONINE; 19 VINDOLININE; 3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; ASPIDOSPERMIDINE; CISPLATIN; EBURENINE; IBOPAMINE; INDOLE ALKALOID; LOCHNERICINE; MELOFUSINE I; MELOMORSINE I; MELOSCANDONINE; N ACYL INDOLINIQUE; QUERBRACHAMINE; TABERSONINE; UNCLASSIFIED DRUG; VENALSTONIDINE; VENALSTONINE; VINCADIFFORMINE; VINCADIFFORMINE NB OXIDE; VOAPHYLLINE;

EID: 79960402459     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.1016/S1875-5364(11)60061-7     Document Type: Article
Times cited : (36)

References (30)
  • 1
    • 37449001322 scopus 로고    scopus 로고
    • How Do Microtubule-Targeted Drugs Work? An Overview [J]
    • Jordan MA, Kamath K How Do Microtubule-Targeted Drugs Work? An Overview [J]. Curr Cancer Drug Targets 2007, 7(8):730-742.
    • (2007) Curr Cancer Drug Targets , vol.7 , Issue.8 , pp. 730-742
    • Jordan, M.A.1    Kamath, K.2
  • 2
    • 0035142850 scopus 로고    scopus 로고
    • Strychnogucines A and B, two new antiplasmodial bisindole alkaloids from Strychnos icaja [J]
    • Frederich M, De Pauw MC, Prosperi C, et al. Strychnogucines A and B, two new antiplasmodial bisindole alkaloids from Strychnos icaja [J]. J Nat Prod 2001, 64(1):12-14.
    • (2001) J Nat Prod , vol.64 , Issue.1 , pp. 12-14
    • Frederich, M.1    De Pauw, M.C.2    Prosperi, C.3
  • 3
    • 0036772968 scopus 로고    scopus 로고
    • Antiplasmodial activity of alkaloids from various Strychnos species [J]
    • Frederich M, Jacquier MJ, Thepenier P, et al. Antiplasmodial activity of alkaloids from various Strychnos species [J]. J Nat Prod 2002, 65(10):1381-1386.
    • (2002) J Nat Prod , vol.65 , Issue.10 , pp. 1381-1386
    • Frederich, M.1    Jacquier, M.J.2    Thepenier, P.3
  • 4
    • 55949087431 scopus 로고    scopus 로고
    • Bipleiophylline, an unprecedented cytotoxic bisindole alkaloid constituted from the bridging of two indole moieties by an aromatic spacer unit [J]
    • Kam TS, Tan SJ, Ng SW, et al. Bipleiophylline, an unprecedented cytotoxic bisindole alkaloid constituted from the bridging of two indole moieties by an aromatic spacer unit [J]. Org Lett 2008, 10(18):3749-3752.
    • (2008) Org Lett , vol.10 , Issue.18 , pp. 3749-3752
    • Kam, T.S.1    Tan, S.J.2    Ng, S.W.3
  • 5
    • 68949086064 scopus 로고    scopus 로고
    • Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor [J]
    • Li GY, Yang T, Luo YG, et al. Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor [J]. Org Lett 2009, 11(16):3714-3717.
    • (2009) Org Lett , vol.11 , Issue.16 , pp. 3714-3717
    • Li, G.Y.1    Yang, T.2    Luo, Y.G.3
  • 6
    • 85193630198 scopus 로고
    • Science Press, Missouri Botanical Garden Press, Beijing and St. Lucis
    • Li PT, Leeuwenberg AJM, Middleton DJ Flora of China[M] 1995, 16:114. Science Press, Missouri Botanical Garden Press, Beijing and St. Lucis.
    • (1995) Flora of China[M] , vol.16 , pp. 114
    • Li, P.T.1    Leeuwenberg, A.J.M.2    Middleton, D.J.3
  • 7
    • 77749254956 scopus 로고    scopus 로고
    • Melotenine A, a cytotoxic monoterpenoid indole alkaloid from Melodinus tenuicaudatus [J]
    • Feng T, Li Y, Liu YP, et al. Melotenine A, a cytotoxic monoterpenoid indole alkaloid from Melodinus tenuicaudatus [J]. Org Lett 2010, 12(5):968-971.
    • (2010) Org Lett , vol.12 , Issue.5 , pp. 968-971
    • Feng, T.1    Li, Y.2    Liu, Y.P.3
  • 8
    • 76049128635 scopus 로고    scopus 로고
    • Melodinines A-G, monoterpenoid indole alkaloids from Melodinus henryi [J]
    • Feng T, Cai XH, Liu YP, et al. Melodinines A-G, monoterpenoid indole alkaloids from Melodinus henryi [J]. J Nat Prod 2010, 73(1):22-26.
    • (2010) J Nat Prod , vol.73 , Issue.1 , pp. 22-26
    • Feng, T.1    Cai, X.H.2    Liu, Y.P.3
  • 9
    • 70350681080 scopus 로고    scopus 로고
    • Melohenines A and B, two unprecedented alkaloids from Melodinus henryi [J]
    • Feng T, Cai XH, Li Y, et al. Melohenines A and B, two unprecedented alkaloids from Melodinus henryi [J]. Org Lett 2009, 11(21):4834-4837.
    • (2009) Org Lett , vol.11 , Issue.21 , pp. 4834-4837
    • Feng, T.1    Cai, X.H.2    Li, Y.3
  • 10
    • 77954073556 scopus 로고    scopus 로고
    • Cytotoxic indole alkaloids from Melodinus tenuicaudatus[J]
    • Feng T, Li Y, Wang YY, et al. Cytotoxic indole alkaloids from Melodinus tenuicaudatus[J]. J Nat Prod 2010, 73(6):1075-1079.
    • (2010) J Nat Prod , vol.73 , Issue.6 , pp. 1075-1079
    • Feng, T.1    Li, Y.2    Wang, Y.Y.3
  • 11
    • 0008972169 scopus 로고
    • Total synthesis of (±1)-tabersonine [J]
    • Ziegler FE, Bennett GB Total synthesis of (±1)-tabersonine [J]. J Am Chem Soc 1971, 93(22):5930-5938.
    • (1971) J Am Chem Soc , vol.93 , Issue.22 , pp. 5930-5938
    • Ziegler, F.E.1    Bennett, G.B.2
  • 12
    • 0028314660 scopus 로고
    • Melomorsine, a new dimeric indoline alkaloid from Melodinus morsei[J]
    • He YL, Chen WM, Feng XZ Melomorsine, a new dimeric indoline alkaloid from Melodinus morsei[J]. J Nat Prod 1994, 57(3):411-413.
    • (1994) J Nat Prod , vol.57 , Issue.3 , pp. 411-413
    • He, Y.L.1    Chen, W.M.2    Feng, X.Z.3
  • 13
    • 44949284965 scopus 로고
    • Alkaloids from Melodinus suaveolens [J]
    • Ye JH, Zhou YL, Huang ZH, et al. Alkaloids from Melodinus suaveolens [J]. Phytochemistry 1991, 30(9):3168-3170.
    • (1991) Phytochemistry , vol.30 , Issue.9 , pp. 3168-3170
    • Ye, J.H.1    Zhou, Y.L.2    Huang, Z.H.3
  • 14
    • 0006292373 scopus 로고
    • Alkaloid production in Catharanthus roseus cell cultures: isolation and characterization of alkaloids from one cell line [J]
    • Kutney JP, Choi LSL, Kolodziejczy P, et al. Alkaloid production in Catharanthus roseus cell cultures: isolation and characterization of alkaloids from one cell line [J]. Phytochemistry 1980, 19(12):2589-2595.
    • (1980) Phytochemistry , vol.19 , Issue.12 , pp. 2589-2595
    • Kutney, J.P.1    Choi, L.S.L.2    Kolodziejczy, P.3
  • 15
    • 0033582790 scopus 로고    scopus 로고
    • Efficient total syntheses of (±)-vincadifformine and (-)-tabersonine [J]
    • Kobayashi S, Peng G, Fukuyama T Efficient total syntheses of (±)-vincadifformine and (-)-tabersonine [J]. Tetrahedron Lett 1999, 40(8):1519-1522.
    • (1999) Tetrahedron Lett , vol.40 , Issue.8 , pp. 1519-1522
    • Kobayashi, S.1    Peng, G.2    Fukuyama, T.3
  • 16
    • 0009250048 scopus 로고
    • Alkaloids from Melodinus hemsleyanus [J]
    • Guo LW, Zhou YL Alkaloids from Melodinus hemsleyanus [J]. Phytochemistry 1993, 34(2):563-566.
    • (1993) Phytochemistry , vol.34 , Issue.2 , pp. 563-566
    • Guo, L.W.1    Zhou, Y.L.2
  • 17
    • 0017853513 scopus 로고
    • Studies on plants containing indole alkaloids. VII. Isolation of several aspidosperma-and vincamine-type alkaloids from the seeds of Amsonia elliptica-roem-schult [J]
    • Aimi N, Asada Y, Sakai S, et al. Studies on plants containing indole alkaloids. VII. Isolation of several aspidosperma-and vincamine-type alkaloids from the seeds of Amsonia elliptica-roem-schult [J]. Chem Pharm Bull 1978, 26(4):1182-1187.
    • (1978) Chem Pharm Bull , vol.26 , Issue.4 , pp. 1182-1187
    • Aimi, N.1    Asada, Y.2    Sakai, S.3
  • 18
    • 85193602434 scopus 로고
    • Chemistry of lochnericine [J]
    • Moza BK, Das KG, Trojanek J, et al. Chemistry of lochnericine [J]. Lloydia 1964, 27(3):267.
    • (1964) Lloydia , vol.27 , Issue.3 , pp. 267
    • Moza, B.K.1    Das, K.G.2    Trojanek, J.3
  • 19
    • 0000988675 scopus 로고
    • Structure of vindolinine [J]
    • Ahond A, Janot MM, Langlois N, et al. Structure of vindolinine [J]. J Am Chem Soc 1974, 96(2):633-634.
    • (1974) J Am Chem Soc , vol.96 , Issue.2 , pp. 633-634
    • Ahond, A.1    Janot, M.M.2    Langlois, N.3
  • 21
    • 0007704644 scopus 로고
    • An asymmetric-systhesis of a quaternary chiral building block from tehylmalonic acid-a preparation of key synthetic intermediates of hunteria-type and aspidosperma-type indole alkaloids [J]
    • Ihara M, Yasui K, Taniguchi N, et al. An asymmetric-systhesis of a quaternary chiral building block from tehylmalonic acid-a preparation of key synthetic intermediates of hunteria-type and aspidosperma-type indole alkaloids [J]. Heterocycles 1990, 31(6):1017-1020.
    • (1990) Heterocycles , vol.31 , Issue.6 , pp. 1017-1020
    • Ihara, M.1    Yasui, K.2    Taniguchi, N.3
  • 22
    • 0028843076 scopus 로고
    • Alkaloids from Tabernaemontana divaricata [J]
    • Kam TS, Anuradha S Alkaloids from Tabernaemontana divaricata [J]. Phytochemistry 1995, 40(1):313-316.
    • (1995) Phytochemistry , vol.40 , Issue.1 , pp. 313-316
    • Kam, T.S.1    Anuradha, S.2
  • 23
    • 0008971265 scopus 로고
    • A new enantioselectlve route to (+)-uebrachamine [J]
    • Asaoka M, Takei H A new enantioselectlve route to (+)-uebrachamine [J]. Heterocycles 1989, 29(2):243-244.
    • (1989) Heterocycles , vol.29 , Issue.2 , pp. 243-244
    • Asaoka, M.1    Takei, H.2
  • 24
    • 0345145789 scopus 로고
    • Methylene-indoles, indolenines et indoleniniums, nouveau rearrangement de la dehydro-1,2 aspidospermidine [J]
    • Hugel G, Levy G, Le Men J Methylene-indoles, indolenines et indoleniniums, nouveau rearrangement de la dehydro-1,2 aspidospermidine [J]. Tetrahedron Lett 1974, 15(36):3109-3112.
    • (1974) Tetrahedron Lett , vol.15 , Issue.36 , pp. 3109-3112
    • Hugel, G.1    Levy, G.2    Le Men, J.3
  • 25
    • 0016720813 scopus 로고
    • Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XXXIV. Monomeric quinolinic Melodinus alkaloids [J]
    • Daudon M, Mehri MH, Plat MM Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XXXIV. Monomeric quinolinic Melodinus alkaloids [J]. J Org Chem 1975, 40(19):2838-2839.
    • (1975) J Org Chem , vol.40 , Issue.19 , pp. 2838-2839
    • Daudon, M.1    Mehri, M.H.2    Plat, M.M.3
  • 26
    • 85009526028 scopus 로고
    • Quinolinic melodinus alkaloids from stem bark Melodinus khasianus [J]
    • Li CM, Zheng HL, Wu SG, et al. Quinolinic melodinus alkaloids from stem bark Melodinus khasianus [J]. Acta Botanic Yunnanica 1994, 16(3):1-3.
    • (1994) Acta Botanic Yunnanica , vol.16 , Issue.3 , pp. 1-3
    • Li, C.M.1    Zheng, H.L.2    Wu, S.G.3
  • 27
    • 0001812732 scopus 로고
    • Quaternary protoberberine alkaloids from Ceratocapnos heterocarpa [J]
    • Suau R, Silva LV, Valpuesta M Quaternary protoberberine alkaloids from Ceratocapnos heterocarpa [J]. Phytochemistry 1993, 34(2):559-561.
    • (1993) Phytochemistry , vol.34 , Issue.2 , pp. 559-561
    • Suau, R.1    Silva, L.V.2    Valpuesta, M.3
  • 28
    • 0002865795 scopus 로고
    • Study on the alkaloids of Melodinus fusiformis [J]
    • He X, Zhou YL, Huang ZH Study on the alkaloids of Melodinus fusiformis [J]. Acta Chim Sin 1992, 50(1):96-101.
    • (1992) Acta Chim Sin , vol.50 , Issue.1 , pp. 96-101
    • He, X.1    Zhou, Y.L.2    Huang, Z.H.3
  • 29
    • 60849091949 scopus 로고    scopus 로고
    • Asymmetric construction of quaternary carbon centers by sequential conjugate addition of lithium amide and in situ alkylation: utility in the synthesis of (-)-aspidospermidine [J]
    • Suzuki M, Kawamoto Y, Sakai T, et al. Asymmetric construction of quaternary carbon centers by sequential conjugate addition of lithium amide and in situ alkylation: utility in the synthesis of (-)-aspidospermidine [J]. Org Lett 2009, 11(3):653-655.
    • (2009) Org Lett , vol.11 , Issue.3 , pp. 653-655
    • Suzuki, M.1    Kawamoto, Y.2    Sakai, T.3
  • 30
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays[J]
    • Mosmann T Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays[J]. J Immunol Methods 1983, 65(1-2):55-63.
    • (1983) J Immunol Methods , vol.65 , Issue.1-2 , pp. 55-63
    • Mosmann, T.1


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