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Volumn 45, Issue 3, 2012, Pages 263-271

Dual inhibition of MAGL and type II topoisomerase by N-phenylmaleimides as a potential strategy to reduce neuroblastoma cell growth

Author keywords

2 Arachidonoylglycerol; Endocannabinoid; Maleimide; Monoacylglycerol lipase; Topoisomerase

Indexed keywords

1 (2 CHLORO 6 METHYLPHENYL) 1H PYRROLE 2,5 DIONE; 1 (2,4,6 TRICHLOROPHENYL) 1H PYRROLE 2,5 DIONE; 1 (2,6 DICHLOROPHENYL) 1H PYRROLE 2,5 DIONE; 2 ARACHIDONOYLGLYCEROL; ACYLGLYCEROL LIPASE; CAY 10488; CAY 10499; DNA TOPOISOMERASE (ATP HYDROLYSING); ENZYME INHIBITOR; JZL 184; MALEIMIDE DERIVATIVE; N PHENYLMALEIMIDE DERIVATIVE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84855760061     PISSN: 09280987     EISSN: 18790720     Source Type: Journal    
DOI: 10.1016/j.ejps.2011.11.011     Document Type: Article
Times cited : (16)

References (52)
  • 1
    • 33646517942 scopus 로고    scopus 로고
    • Accumulation of hydrogen peroxide is an early and crucial step for paclitaxel-induced cancer cell death both in vitro and in vivo
    • J. Alexandre, F. Batteux, C. Nicco, C. Chereau, A. Laurent, L. Guillevin, B. Weill, and F. Goldwasser Accumulation of hydrogen peroxide is an early and crucial step for paclitaxel-induced cancer cell death both in vitro and in vivo Int. J. Cancer 119 2006 41 48
    • (2006) Int. J. Cancer , vol.119 , pp. 41-48
    • Alexandre, J.1    Batteux, F.2    Nicco, C.3    Chereau, C.4    Laurent, A.5    Guillevin, L.6    Weill, B.7    Goldwasser, F.8
  • 2
    • 9444280832 scopus 로고    scopus 로고
    • A new strategy to block tumor growth by inhibiting endocannabinoid inactivation
    • DOI 10.1096/fj.04-1754fje
    • M. Bifulco, C. Laezza, M. Valenti, A. Ligresti, G. Portella, and V. Di Marzo A new strategy to block tumor growth by inhibiting endocannabinoid inactivation FASEB J. 18 2004 1606 1608 (Pubitemid 39561648)
    • (2004) FASEB Journal , vol.18 , Issue.13 , pp. 1606-1608
    • Bifulco, M.1    Laezza, C.2    Valenti, M.3    Ligresti, A.4    Portella, G.5    Di Marzo, V.6
  • 3
    • 34447619258 scopus 로고    scopus 로고
    • Agonist selective modulation of tyrosine hydroxylase expression by cannabinoid ligands in a murine neuroblastoma cell line
    • DOI 10.1111/j.1471-4159.2007.04679.x
    • B. Bosier, S. Tilleux, M. Najimi, D.M. Lambert, and E. Hermans Agonist selective modulation of tyrosine hydroxylase expression by cannabinoid ligands in a murine neuroblastoma cell line J. Neurochem. 102 2007 1996 2007 (Pubitemid 47329272)
    • (2007) Journal of Neurochemistry , vol.102 , Issue.6 , pp. 1996-2007
    • Bosier, B.1    Tilleux, S.2    Najimi, M.3    Lambert, D.M.4    Hermans, E.5
  • 4
    • 55749113512 scopus 로고    scopus 로고
    • Reciprocal influences of CB1 cannabinoid receptor agonists on ERK and JNK signalling in N1E-115 cells
    • B. Bosier, D.M. Lambert, and E. Hermans Reciprocal influences of CB1 cannabinoid receptor agonists on ERK and JNK signalling in N1E-115 cells FEBS Lett. 582 2008 3861 3867
    • (2008) FEBS Lett. , vol.582 , pp. 3861-3867
    • Bosier, B.1    Lambert, D.M.2    Hermans, E.3
  • 6
    • 0034887619 scopus 로고    scopus 로고
    • DNA relaxation and cleavage assays to study topoisomerase i inhibitors
    • Bailly. Christian DNA relaxation and cleavage assays to study topoisomerase I inhibitors Methods Enzymol. 340 2001 610 623
    • (2001) Methods Enzymol. , vol.340 , pp. 610-623
    • Christian, B.1
  • 7
    • 0033665922 scopus 로고    scopus 로고
    • Endocannabinoids and fatty acid amides in cancer, inflammation and related disorders
    • L. De Petrocellis, D. Melck, T. Bisogno, and V. Di Marzo Endocannabinoids and fatty acid amides in cancer, inflammation and related disorders Chem. Phys. Lipids 108 2000 191 209
    • (2000) Chem. Phys. Lipids , vol.108 , pp. 191-209
    • De Petrocellis, L.1    Melck, D.2    Bisogno, T.3    Di Marzo, V.4
  • 8
    • 34250378332 scopus 로고    scopus 로고
    • Opposing actions of endocannabinoids on cholangiocarcinoma growth: Recruitment of Fas and Fas ligand to lipid rafts
    • DOI 10.1074/jbc.M608238200
    • S. Demorrow, S. Glaser, H. Francis, J. Venter, B. Vaculin, S. Vaculin, and G. Alpini Opposing actions of endocannabinoids on cholangiocarcinoma growth: recruitment of Fas and Fas ligand to lipid rafts J. Biol. Chem. 282 2007 13098 13113 (Pubitemid 47100640)
    • (2007) Journal of Biological Chemistry , vol.282 , Issue.17 , pp. 13098-13113
    • DeMorrow, S.1    Glaser, S.2    Francis, H.3    Venter, J.4    Vaculin, B.5    Vaculin, S.6    Alpini, G.7
  • 9
    • 0031048819 scopus 로고    scopus 로고
    • Methyl arachidonyl fluorophosphonate: A potent irreversible inhibitor of anandamide amidase
    • DOI 10.1016/S0006-2952(96)00830-1, PII S0006295296008301
    • D.G. Deutsch, R. Omeir, G. Arreaza, D. Salehani, G.D. Prestwich, Z. Huang, and A. Howlett Methyl arachidonyl fluorophosphonate: a potent irreversible inhibitor of anandamide amidase Biochem. Pharmacol. 53 1997 255 260 (Pubitemid 27112941)
    • (1997) Biochemical Pharmacology , vol.53 , Issue.3 , pp. 255-260
    • Deutsch, D.G.1    Omeir, R.2    Arreaza, G.3    Salehani, D.4    Prestwich, G.D.5    Huang, Z.6    Howlett, A.7
  • 10
    • 0034001560 scopus 로고    scopus 로고
    • Cannabimimetic fatty acid derivatives in cancer and inflammation
    • DOI 10.1016/S0090-6980(00)00054-X, PII S009069800000054X
    • V. Di Marzo, D. Melck, L. De Petrocellis, and T. Bisogno Cannabimimetic fatty acid derivatives in cancer and inflammation Prostaglandins Other Lipid Mediat. 61 2000 43 61 (Pubitemid 30216488)
    • (2000) Prostaglandins and Other Lipid Mediators , vol.61 , Issue.1-2 , pp. 43-61
    • Di Marzo, V.1    Melck, D.2    De Petrocellis, L.3    Bisogno, T.4
  • 13
    • 0042431524 scopus 로고    scopus 로고
    • Inhibition of C6 glioma cell proliferation by anandamide, 1-arachidonoylglycerol, and by a water soluble phosphate ester of anandamide: Variability in response and involvement of arachidonic acid
    • DOI 10.1016/S0006-2952(03)00392-7
    • C.J. Fowler, K.O. Jonsson, A. Andersson, J. Juntunen, T. Jarvinen, S. Vandevoorde, D.M. Lambert, J.C. Jerman, and D. Smart Inhibition of C6 glioma cell proliferation by anandamide, 1-arachidonoylglycerol, and by a water soluble phosphate ester of anandamide: variability in response and involvement of arachidonic acid Biochem. Pharmacol. 66 2003 757 767 (Pubitemid 37011414)
    • (2003) Biochemical Pharmacology , vol.66 , Issue.5 , pp. 757-767
    • Fowler, C.J.1    Jonsson, K.-O.2    Andersson, A.3    Juntunen, J.4    Jarvinen, T.5    Vandevoorde, S.6    Lambert, D.M.7    Jerman, J.C.8    Smart, D.9
  • 14
    • 79960336157 scopus 로고    scopus 로고
    • The endocannabinoid system and cancer: Therapeutic implications
    • J. Guindon, and A.G. Hohmann The endocannabinoid system and cancer: therapeutic implications Br. J. Pharmacol. 163 2011 1447 1463
    • (2011) Br. J. Pharmacol. , vol.163 , pp. 1447-1463
    • Guindon, J.1    Hohmann, A.G.2
  • 15
    • 78650423565 scopus 로고    scopus 로고
    • Antagonism of cytotoxic chemotherapy in neuroblastoma cell lines by 13-cis-retinoic acid is mediated by the antiapoptotic Bcl-2 family proteins
    • M.D. Hadjidaniel, and C.P. Reynolds Antagonism of cytotoxic chemotherapy in neuroblastoma cell lines by 13-cis-retinoic acid is mediated by the antiapoptotic Bcl-2 family proteins Mol. Cancer Ther. 9 2010 3164 3174
    • (2010) Mol. Cancer Ther. , vol.9 , pp. 3164-3174
    • Hadjidaniel, M.D.1    Reynolds, C.P.2
  • 16
    • 37549055477 scopus 로고    scopus 로고
    • The nitrone disodium 2, 4-sulphophenyl-N-tert-butylnitrone is without cytoprotective effect on sodium nitroprusside-induced cell death in N1E-115 neuroblastoma cells in vitro
    • A.H. Hainsworth, N. Bhuiyan, and A.R. Green The nitrone disodium 2, 4-sulphophenyl-N-tert-butylnitrone is without cytoprotective effect on sodium nitroprusside-induced cell death in N1E-115 neuroblastoma cells in vitro J. Cereb. Blood Flow Metab. 28 2008 24 28
    • (2008) J. Cereb. Blood Flow Metab. , vol.28 , pp. 24-28
    • Hainsworth, A.H.1    Bhuiyan, N.2    Green, A.R.3
  • 17
    • 80055033752 scopus 로고    scopus 로고
    • Increasing antiproliferative properties of endocannabinoids in N1E-115 neuroblastoma cells through inhibition of their metabolism
    • L. Hamtiaux, L. Hansoulle, N. Dauguet, G.G. Muccioli, B. Gallez, and D.M. Lambert Increasing antiproliferative properties of endocannabinoids in N1E-115 neuroblastoma cells through inhibition of their metabolism PLoS ONE 6 10 2011 e26823
    • (2011) PLoS ONE , vol.6 , Issue.10 , pp. 26823
    • Hamtiaux, L.1    Hansoulle, L.2    Dauguet, N.3    Muccioli, G.G.4    Gallez, B.5    Lambert, D.M.6
  • 18
    • 0032168167 scopus 로고    scopus 로고
    • Etoposide: Four decades of development of a topoisomerase II inhibitor
    • DOI 10.1016/S0959-8049(98)00228-7, PII S0959804998002287
    • K.R. Hande Etoposide: four decades of development of a topoisomerase II inhibitor Eur. J. Cancer 34 1998 1514 1521 (Pubitemid 28446331)
    • (1998) European Journal of Cancer , vol.34 , Issue.10 , pp. 1514-1521
    • Hande, K.R.1
  • 20
    • 0009848001 scopus 로고    scopus 로고
    • DNA topoisomerases as anticancer drug targets: From the laboratory to the clinic
    • J.A. Holden DNA topoisomerases as anticancer drug targets: from the laboratory to the clinic Curr. Med. Chem. Anticancer Agents 1 2001 1 25
    • (2001) Curr. Med. Chem. Anticancer Agents , vol.1 , pp. 1-25
    • Holden, J.A.1
  • 21
    • 0035200613 scopus 로고    scopus 로고
    • Inhibition of rat C6 glioma cell proliferation by endogenous and synthetic cannabinoids. Relative involvement of cannabinoid and vanilloid receptors
    • S.O. Jacobsson, T. Wallin, and C.J. Fowler Inhibition of rat C6 glioma cell proliferation by endogenous and synthetic cannabinoids. Relative involvement of cannabinoid and vanilloid receptors J. Pharmacol. Exp. Ther. 299 2001 951 959 (Pubitemid 33104965)
    • (2001) Journal of Pharmacology and Experimental Therapeutics , vol.299 , Issue.3 , pp. 951-959
    • Jacobsson, S.O.P.1    Wallin, T.2    Fowler, C.J.3
  • 23
    • 0038105281 scopus 로고    scopus 로고
    • Rationally designed hydrolytically activated etoposide prodrugs, a novel strategy for the treatment of neuroblastoma
    • DOI 10.1016/S0304-3835(03)00106-X
    • B. Lange, U. Schroeder, N. Huebener, J. Jikai, J. Wenkel, A. Strandsby, W. Wrasidlo, G. Gaedicke, and H.N. Lode Rationally designed hydrolytically activated etoposide prodrugs, a novel strategy for the treatment of neuroblastoma Cancer Lett. 197 2003 225 230 (Pubitemid 36860015)
    • (2003) Cancer Letters , vol.197 , Issue.1-2 , pp. 225-230
    • Lange, B.1    Schroeder, U.2    Huebener, N.3    Jikai, J.4    Wenkel, J.5    Strandsby, A.6    Wrasidlo, W.7    Gaedicke, G.8    Lode, H.N.9
  • 25
    • 84863115225 scopus 로고    scopus 로고
    • Design and synthesis of novel camptothecin/5-fluorouracil conjugates as cytotoxic agents
    • Liu, Y.Q., Dai, W., Yang, L., Li, H.Y., 2011. Design and synthesis of novel camptothecin/5-fluorouracil conjugates as cytotoxic agents. Nat. Prod. Res. pp. 1-10.
    • (2011) Nat. Prod. Res. , pp. 1-10
    • Liu, Y.Q.1    Dai, W.2    Yang, L.3    Li, H.Y.4
  • 27
    • 0034644769 scopus 로고    scopus 로고
    • Anandamide induces apoptosis in human cells via vanilloid receptors. Evidence for a protective role of cannabinoid receptors
    • M. Maccarrone, T. Lorenzon, M. Bari, G. Melino, and A. Finazzi-Agro Anandamide induces apoptosis in human cells via vanilloid receptors. Evidence for a protective role of cannabinoid receptors J. Biol. Chem. 275 2000 31938 31945
    • (2000) J. Biol. Chem. , vol.275 , pp. 31938-31945
    • MacCarrone, M.1    Lorenzon, T.2    Bari, M.3    Melino, G.4    Finazzi-Agro, A.5
  • 28
    • 72249083920 scopus 로고    scopus 로고
    • Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors
    • N. Matuszak, G.G. Muccioli, G. Labar, and D.M. Lambert Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors J. Med. Chem. 52 2009 7410 7420
    • (2009) J. Med. Chem. , vol.52 , pp. 7410-7420
    • Matuszak, N.1    Muccioli, G.G.2    Labar, G.3    Lambert, D.M.4
  • 29
    • 0038751939 scopus 로고    scopus 로고
    • Anti-proliferative and apoptotic effects of anandamide in human prostatic cancer cell lines: Implication of epidermal growth factor receptor down-regulation and ceramide production
    • DOI 10.1002/pros.10190
    • M. Mimeault, N. Pommery, N. Wattez, C. Bailly, and J.P. Henichart Anti-proliferative and apoptotic effects of anandamide in human prostatic cancer cell lines: implication of epidermal growth factor receptor down-regulation and ceramide production Prostate 56 2003 1 12 (Pubitemid 36613150)
    • (2003) Prostate , vol.56 , Issue.1 , pp. 1-12
    • Mimeault, M.1    Pommery, N.2    Wattez, N.3    Bailly, C.4    Henichart, J.-P.5
  • 30
    • 0032723873 scopus 로고    scopus 로고
    • Yeast topoisomerase II is inhibited by etoposide after hydrolyzing the first ATP and before releasing the second ADP
    • S.K. Morris, and J.E. Lindsley Yeast topoisomerase II is inhibited by etoposide after hydrolyzing the first ATP and before releasing the second ADP J. Biol. Chem. 274 1999 30690 30696
    • (1999) J. Biol. Chem. , vol.274 , pp. 30690-30696
    • Morris, S.K.1    Lindsley, J.E.2
  • 31
    • 77954819357 scopus 로고    scopus 로고
    • Endocannabinoid biosynthesis and inactivation, from simple to complex
    • G.G. Muccioli Endocannabinoid biosynthesis and inactivation, from simple to complex Drug Discovery Today 15 2010 474 483
    • (2010) Drug Discovery Today , vol.15 , pp. 474-483
    • Muccioli, G.G.1
  • 32
    • 59449101653 scopus 로고    scopus 로고
    • CAY10499, a novel monoglyceride lipase inhibitor evidenced by an expeditious MGL assay
    • G.G. Muccioli, G. Labar, and D.M. Lambert CAY10499, a novel monoglyceride lipase inhibitor evidenced by an expeditious MGL assay ChemBioChem 9 2008 2704 2710
    • (2008) ChemBioChem , vol.9 , pp. 2704-2710
    • Muccioli, G.G.1    Labar, G.2    Lambert, D.M.3
  • 33
    • 77950020507 scopus 로고    scopus 로고
    • Neuronal models for evaluation of proliferation in vitro using high content screening
    • W.R. Mundy, N.M. Radio, and T.M. Freudenrich Neuronal models for evaluation of proliferation in vitro using high content screening Toxicology 270 2010 121 130
    • (2010) Toxicology , vol.270 , pp. 121-130
    • Mundy, W.R.1    Radio, N.M.2    Freudenrich, T.M.3
  • 35
    • 73149109062 scopus 로고    scopus 로고
    • Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis
    • D.K. Nomura, J.Z. Long, S. Niessen, H.S. Hoover, S.W. Ng, and B.F. Cravatt Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis Cell 140 2010 49 61
    • (2010) Cell , vol.140 , pp. 49-61
    • Nomura, D.K.1    Long, J.Z.2    Niessen, S.3    Hoover, H.S.4    Ng, S.W.5    Cravatt, B.F.6
  • 36
    • 59449100511 scopus 로고    scopus 로고
    • Protection against amyloid beta cytotoxicity by sulforaphane: Role of the proteasome
    • H.M. Park, J.A. Kim, and M.K. Kwak Protection against amyloid beta cytotoxicity by sulforaphane: role of the proteasome Arch. Pharm. Res. 32 2009 109 115
    • (2009) Arch. Pharm. Res. , vol.32 , pp. 109-115
    • Park, H.M.1    Kim, J.A.2    Kwak, M.K.3
  • 37
    • 79952559236 scopus 로고    scopus 로고
    • Antiproliferative mechanism of a cannabinoid agonist by cell cycle arrest in human gastric cancer cells
    • J.M. Park, X.S. Xian, M.G. Choi, H. Park, Y.K. Cho, I.S. Lee, S.W. Kim, and I.S. Chung Antiproliferative mechanism of a cannabinoid agonist by cell cycle arrest in human gastric cancer cells J. Cell. Biochem. 112 2011 1192 1205
    • (2011) J. Cell. Biochem. , vol.112 , pp. 1192-1205
    • Park, J.M.1    Xian, X.S.2    Choi, M.G.3    Park, H.4    Cho, Y.K.5    Lee, I.S.6    Kim, S.W.7    Chung, I.S.8
  • 39
    • 0025148030 scopus 로고
    • The effects of single dose oral hydralazine on blood flow through human lung tumours
    • DOI 10.1016/0167-8140(90)90108-9
    • N.P. Rowell, M.A. Flower, V.R. McCready, B. Cronin, and A. Horwich The effects of single dose oral hydralazine on blood flow through human lung tumours Radiother. Oncol. 18 1990 283 292 (Pubitemid 20264673)
    • (1990) Radiotherapy and Oncology , vol.18 , Issue.4 , pp. 283-292
    • Rowell, N.P.1    Flower, M.A.2    McCready, V.R.3    Cronin, B.4    Horwich, A.5
  • 40
    • 24944508307 scopus 로고    scopus 로고
    • Characterization of the sulfhydryl-sensitive site in the enzyme responsible for hydrolysis of 2-arachidonoyl-glycerol in rat cerebellar membranes
    • DOI 10.1016/j.chembiol.2005.04.013
    • S.M. Saario, O.M. Salo, T. Nevalainen, A. Poso, J.T. Laitinen, T. Jarvinen, and R. Niemi Characterization of the sulfhydryl-sensitive site in the enzyme responsible for hydrolysis of 2-arachidonoyl-glycerol in rat cerebellar membranes Chem. Biol. 12 2005 649 656 (Pubitemid 43142042)
    • (2005) Chemistry and Biology , vol.12 , Issue.6 , pp. 649-656
    • Saario, S.M.1    Salo, O.M.H.2    Nevalainen, T.3    Poso, A.4    Laitinen, J.T.5    Jarvinen, T.6    Niemi, R.7
  • 41
    • 78650805812 scopus 로고    scopus 로고
    • Cannabinoids attenuate cancer pain and proliferation in a mouse model
    • N. Saghafi, D.K. Lam, and B.L. Schmidt Cannabinoids attenuate cancer pain and proliferation in a mouse model Neurosci. Lett. 488 2011 247 251
    • (2011) Neurosci. Lett. , vol.488 , pp. 247-251
    • Saghafi, N.1    Lam, D.K.2    Schmidt, B.L.3
  • 43
    • 0030007125 scopus 로고    scopus 로고
    • Mapping of DNA topoisomerase II poisons (etoposide, clerocidin) and catalytic inhibitors (aclarubicin, ICRF-187) to four distinct steps in the topoisomerase II catalytic cycle
    • DOI 10.1016/0006-2952(95)02241-4
    • M. Sehested, and P.B. Jensen Mapping of DNA topoisomerase II poisons (etoposide, clerocidin) and catalytic inhibitors (aclarubicin, ICRF-187) to four distinct steps in the topoisomerase II catalytic cycle Biochem. Pharmacol. 51 1996 879 886 (Pubitemid 26111144)
    • (1996) Biochemical Pharmacology , vol.51 , Issue.7 , pp. 879-886
    • Sehested, M.1    Jensen, P.B.2
  • 45
    • 34548499520 scopus 로고    scopus 로고
    • The endocannabinoid 2-arachidonoyl glycerol induces death of hepatic stellate cells via mitochondrial reactive oxygen species
    • DOI 10.1096/fj.06-7717com
    • S.V. Siegmund, T. Qian, M.S. de, J. Harvey-White, G. Kunos, K.Y. Vinod, B. Hungund, and R.F. Schwabe The endocannabinoid 2-arachidonoyl glycerol induces death of hepatic stellate cells via mitochondrial reactive oxygen species FASEB J. 21 2007 2798 2806 (Pubitemid 47372747)
    • (2007) FASEB Journal , vol.21 , Issue.11 , pp. 2798-2806
    • Siegmund, S.V.1    Qian, T.2    De Minicis, S.3    Harvey-White, J.4    Kunos, G.5    Vinod, K.Y.6    Hungund, B.7    Schwabe, R.F.8
  • 46
    • 0026425619 scopus 로고
    • Inhibition of topoisomerase II by antitumor agents bis(2, 6-dioxopiperazine) derivatives
    • K. Tanabe, Y. Ikegami, R. Ishida, and T. Andoh Inhibition of topoisomerase II by antitumor agents bis(2, 6-dioxopiperazine) derivatives Cancer Res. 51 1991 4903 4908
    • (1991) Cancer Res. , vol.51 , pp. 4903-4908
    • Tanabe, K.1    Ikegami, Y.2    Ishida, R.3    Andoh, T.4
  • 47
    • 0027208041 scopus 로고
    • Antitumor agents. 3. Synthesis and biological activity of 4β-alkyl derivatives containing hydroxy, amino, and amido groups of 4'-O-demethyl-4- desoxypodophyllotoxin as antitumor agents
    • T. Terada, K. Fujimoto, M. Nomura, J. Yamashita, K. Wierzba, R. Yamazaki, J. Shibata, Y. Sugimoto, Y. Yamada, and T. Kobunai Antitumor agents. 3. Synthesis and biological activity of 4 beta-alkyl derivatives containing hydroxy, amino, and amido groups of 4′-O-demethyl-4-desoxypodophyllotoxin as antitumor agents J. Med. Chem. 36 1993 1689 1699 (Pubitemid 23191296)
    • (1993) Journal of Medicinal Chemistry , vol.36 , Issue.12 , pp. 1689-1699
    • Terada, T.1    Fujimoto, K.2    Nomura, M.3    Yamashita, Y.-I.4    Wierzba, K.5    Yamazaki, R.6    Shibata, J.7    Sugimoto, Y.8    Yamada, Y.9
  • 49
    • 78049284266 scopus 로고    scopus 로고
    • Synthesis of 3-fluoro-6-S-(2-S-pyridyl) nucleosides as potential lead cytostatic agents
    • E. Tsoukala, N. Tzioumaki, S. Manta, A. Riga, J. Balzarini, and D. Komiotis Synthesis of 3-fluoro-6-S-(2-S-pyridyl) nucleosides as potential lead cytostatic agents Bioorg. Chem. 38 2010 285 293
    • (2010) Bioorg. Chem. , vol.38 , pp. 285-293
    • Tsoukala, E.1    Tzioumaki, N.2    Manta, S.3    Riga, A.4    Balzarini, J.5    Komiotis, D.6
  • 51
  • 52


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