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Volumn 2, Issue 9, 2011, Pages 526-535

3-(Fur-2-yl)-10-(2-phenylethyl)-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)- one, a novel adenosine receptor antagonist with A2A-mediated neuroprotective effects

Author keywords

A2AAR antagonists; Cell viability; Human neuroblastoma cells; Neuroprotection; Neurotoxins; PC12 cells

Indexed keywords

(3 ( FUR 2 YL) 10 ( 2 PHENYLETHYL) [1,2,4]TRIAZINOL[4,3 A]BENZIMIDAZOL 4(10H) ONE); 1 METHYL 4 PHENYLPYRIDINIUM; 4 [2 [7 AMINO 2 (2 FURYL) 1,2,4 TRIAZOLO[2,3 A][1,3,5]TRIAZIN 5 YLAMINO]ETHYL]PHENOL; ADENOSINE 5' (N ETHYLCARBOXAMIDE); ADENOSINE A2A RECEPTOR ANTAGONIST; METHAMPHETAMINE; NEUROPROTECTIVE AGENT; TRYPAN BLUE; UNCLASSIFIED DRUG; 3 (FUR 2 YL) 10 (2 PHENYLETHYL) (1,2,4)TRIAZINO(4,3 A)BENZIMIDAZOL 4(10H) ONE; 3-(FUR-2-YL)-10-(2-PHENYLETHYL)-(1,2,4)TRIAZINO(4,3-A)BENZIMIDAZOL-4(10H)-ONE; 4 AMINOBUTYRIC ACID A RECEPTOR; ADENOSINE A1 RECEPTOR; ADENOSINE A2 RECEPTOR ANTAGONIST; ADENOSINE A2A RECEPTOR; BENZIMIDAZOLE DERIVATIVE; CYCLIC AMP; DOPAMINE 2 RECEPTOR; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NEUROTOXIN; TRIAZINE DERIVATIVE;

EID: 84876034737     PISSN: None     EISSN: 19487193     Source Type: Journal    
DOI: 10.1021/cn200036s     Document Type: Article
Times cited : (7)

References (56)
  • 1
    • 0031833150 scopus 로고    scopus 로고
    • Adenosine receptors: New opportunities for future drugs
    • Poulsen, S. A., and Quinn, R. J. (1998) Adenosine receptors: new opportunities for future drugs. Bioorg. Med. Chem. 6, 619-641.
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 619-641
    • Poulsen, S.A.1    Quinn, R.J.2
  • 3
    • 0035209620 scopus 로고    scopus 로고
    • International union of pharmacology. XXV. Nomenclature and classification of adenosine receptors
    • Fredholm, B. B., IJzerman, A. P., Jacobson, K. A., Klotz, K.-N., and Linden, J. (2001) International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors. Pharmacol. Rev. 53, 527-552.
    • (2001) Pharmacol. Rev. , vol.53 , pp. 527-552
    • Fredholm, B.B.1    Ijzerman, A.P.2    Jacobson, K.A.3    Klotz, K.-N.4    Linden, J.5
  • 4
    • 0033851227 scopus 로고    scopus 로고
    • Human adenosine A(1), A(2A), A(2B), and A(3) receptors expressed in Chinese hamster ovary cells all mediate the phosphorylation of extracellular-regulated kinase 1/2
    • Schulte, G., and Fredholm, B. B. (2000) Human adenosine A(1), A(2A), A(2B), and A(3) receptors expressed in Chinese hamster ovary cells all mediate the phosphorylation of extracellular-regulated kinase 1/2. Mol. Pharmacol. 58, 477-482.
    • (2000) Mol. Pharmacol. , vol.58 , pp. 477-482
    • Schulte, G.1    Fredholm, B.B.2
  • 5
    • 33644770260 scopus 로고    scopus 로고
    • Adenosine receptors as therapeutic targets
    • Jacobson, K. A., and Gao, Z. G. (2006) Adenosine receptors as therapeutic targets. Nat. Rev. Drug Discovery 5, 247-264.
    • (2006) Nat. Rev. Drug Discovery , vol.5 , pp. 247-264
    • Jacobson, K.A.1    Gao, Z.G.2
  • 6
    • 33644674438 scopus 로고    scopus 로고
    • Progress in the pursuit of therapeutic adenosine receptor antagonists
    • Moro, S., Gao, Z. G., Jacobson, K. A., and Spalluto, G. (2006) Progress in the pursuit of therapeutic adenosine receptor antagonists. Med. Res. Rev. 26, 131-159.
    • (2006) Med. Res. Rev. , vol.26 , pp. 131-159
    • Moro, S.1    Gao, Z.G.2    Jacobson, K.A.3    Spalluto, G.4
  • 7
    • 0036973951 scopus 로고    scopus 로고
    • Adenosine receptors in the nervous system: Pathophysiological implications
    • Ribeiro, J. A., Sebastiao, A. M., and de Mendonca, A. (2002) Adenosine receptors in the nervous system: pathophysiological implications. Prog. Neurobiol. 68, 377-392.
    • (2002) Prog. Neurobiol. , vol.68 , pp. 377-392
    • Ribeiro, J.A.1    Sebastiao, A.M.2    De Mendonca, A.3
  • 8
    • 0031007914 scopus 로고    scopus 로고
    • A1-adenosine receptor antagonists
    • Muller, C. E. (1997) A1-adenosine receptor antagonists. Expert Opin. Ther. Pat. 7, 419-440.
    • (1997) Expert Opin. Ther. Pat. , vol.7 , pp. 419-440
    • Muller, C.E.1
  • 9
    • 0033639016 scopus 로고    scopus 로고
    • A2A-adenosine receptor antagonists-future drugs for Parkinson's disease?
    • Muller, C. E. (2000) A2A-adenosine receptor antagonists-future drugs for Parkinson's disease?. Drugs Future 25, 1043-1052.
    • (2000) Drugs Future , vol.25 , pp. 1043-1052
    • Muller, C.E.1
  • 10
    • 38749132550 scopus 로고    scopus 로고
    • Adenosine receptor antagonists: Translating medicinal chemistry and pharmacology into clinical utility
    • Baraldi, P. G., Tabrizi, M. A., Gessi, S., and Borea, P. A. (2008) Adenosine receptor antagonists: translating medicinal chemistry and pharmacology into clinical utility. Chem. Rev. 108, 238-263.
    • (2008) Chem. Rev. , vol.108 , pp. 238-263
    • Baraldi, P.G.1    Tabrizi, M.A.2    Gessi, S.3    Borea, P.A.4
  • 11
    • 34548295509 scopus 로고    scopus 로고
    • Therapeutic potential of adenosine receptor antagonists and agonists
    • Press, N. J., Gessi, S., Borea, P. A., and Polosa, R. (2007) Therapeutic potential of adenosine receptor antagonists and agonists. Expert Opin. Ther. Pat. 17, 979-991.
    • (2007) Expert Opin. Ther. Pat. , vol.17 , pp. 979-991
    • Press, N.J.1    Gessi, S.2    Borea, P.A.3    Polosa, R.4
  • 12
    • 70349327971 scopus 로고    scopus 로고
    • Adenosine A2A receptors and Parkinson's disease
    • Morelli, M., Carta, A. R., and Jenner, P. (2009) Adenosine A2A receptors and Parkinson's disease. Handb. Exp. Pharmacol. 193, 589-615.
    • (2009) Handb. Exp. Pharmacol. , vol.193 , pp. 589-615
    • Morelli, M.1    Carta, A.R.2    Jenner, P.3
  • 13
    • 47349089093 scopus 로고    scopus 로고
    • A critical evaluation of adenosine A2A receptors as potentially "druggable" targets in Huntington's disease
    • Popoli, P., Blum, D., Domenici, M. R., Burnouf, S., and Chern, Y. (2008) A critical evaluation of adenosine A2A receptors as potentially "druggable" targets in Huntington's disease. Curr. Pharm. Des. 14, 1500-1511.
    • (2008) Curr. Pharm. Des. , vol.14 , pp. 1500-1511
    • Popoli, P.1    Blum, D.2    Domenici, M.R.3    Burnouf, S.4    Chern, Y.5
  • 14
    • 62249214963 scopus 로고    scopus 로고
    • Adenosine antagonists reverse the cataleptic effects of haloperidol: Implications for the treatment of Parkinson's disease
    • Trevitt, J., Vallance, C., Harris, A., and Goode, T. (2009) Adenosine antagonists reverse the cataleptic effects of haloperidol: implications for the treatment of Parkinson's disease. Pharmacol., Biochem. Behav. 92, 521-527.
    • (2009) Pharmacol., Biochem. Behav. , vol.92 , pp. 521-527
    • Trevitt, J.1    Vallance, C.2    Harris, A.3    Goode, T.4
  • 15
    • 0028321498 scopus 로고
    • CGS 15943, an adenosine receptor antagonist, reduces cerebral ischemic injury in the Mongolian gerbil
    • Gao, Y., and Phillis, J. W. (1994) CGS 15943, an adenosine receptor antagonist, reduces cerebral ischemic injury in the Mongolian gerbil. Life Sci. 55, 61-65.
    • (1994) Life Sci. , vol.55 , pp. 61-65
    • Gao, Y.1    Phillis, J.W.2
  • 16
    • 0032217044 scopus 로고    scopus 로고
    • Blockade of adenosine A2A receptors by SCH 58261 results in neuroprotective effects in cerebral ischemia in rats
    • Monopoli, A. L. G., Forlani, A., Mattavelli, A., and Ongini, E. (1998) Blockade of adenosine A2A receptors by SCH 58261 results in neuroprotective effects in cerebral ischemia in rats. Neuro Report 9, 3955-3959.
    • (1998) Neuro Report , vol.9 , pp. 3955-3959
    • Monopoli, A.L.G.1    Forlani, A.2    Mattavelli, A.3    Ongini, E.4
  • 19
    • 16344372309 scopus 로고    scopus 로고
    • Neuroprotection by adenosine in the brain: From A1 receptor activation to A2A receptor blockade
    • Cuhna, R. A. (2005) Neuroprotection by adenosine in the brain: from A1 receptor activation to A2A receptor blockade. Purinergic Signalling 1, 111-134.
    • (2005) Purinergic Signalling , vol.1 , pp. 111-134
    • Cuhna, R.A.1
  • 20
    • 1842510008 scopus 로고    scopus 로고
    • Adenosine A2A receptor antagonists prevent the increase in striatal glutamate levels induced by glutamate uptake inhibitors
    • Pintor, A., Galluzzo, M., Grieco, R., Pezzola, A., Reggio, R., and Popoli, P. (2004) Adenosine A2A receptor antagonists prevent the increase in striatal glutamate levels induced by glutamate uptake inhibitors. J. Neurochem. 89, 152-6.
    • (2004) J. Neurochem. , vol.89 , pp. 152-156
    • Pintor, A.1    Galluzzo, M.2    Grieco, R.3    Pezzola, A.4    Reggio, R.5    Popoli, P.6
  • 21
    • 0028972137 scopus 로고
    • Adenosine A2A receptor stimulation enhances striatal extracellular glutamate levels in rats
    • Popoli, P., Betto, P., Reggio, R., and Ricciarello, G. (1995) Adenosine A2A receptor stimulation enhances striatal extracellular glutamate levels in rats. Eur. J. Pharmacol. 287, 215-217.
    • (1995) Eur. J. Pharmacol. , vol.287 , pp. 215-217
    • Popoli, P.1    Betto, P.2    Reggio, R.3    Ricciarello, G.4
  • 22
    • 70349331090 scopus 로고    scopus 로고
    • Adenosine receptors and neurological disease: Neuroprotection and neurodegeneration
    • Stone, T.W., Ceruti, S., and Abbracchio, M. P. (2009) Adenosine receptors and neurological disease: neuroprotection and neurodegeneration. Handb. Exp. Pharmacol. 193, 535-587.
    • (2009) Handb. Exp. Pharmacol. , vol.193 , pp. 535-587
    • Stone, T.W.1    Ceruti, S.2    Abbracchio, M.P.3
  • 23
    • 0028289758 scopus 로고
    • The effect of theophylline on parkinsonian symptoms
    • Mally, J., and Stone, T. W. (1994) The effect of theophylline on parkinsonian symptoms. J. Pharm. Pharmacol. 46, 515-517.
    • (1994) J. Pharm. Pharmacol. , vol.46 , pp. 515-517
    • Mally, J.1    Stone, T.W.2
  • 24
    • 0030463754 scopus 로고    scopus 로고
    • Potential role of adenosine antagonist therapy in pathological tremor disorders
    • Mally, J., and Stone, T. W. (1996) Potential role of adenosine antagonist therapy in pathological tremor disorders. Pharmacol. Ther. 72, 243-250.
    • (1996) Pharmacol. Ther. , vol.72 , pp. 243-250
    • Mally, J.1    Stone, T.W.2
  • 25
    • 0031756703 scopus 로고    scopus 로고
    • Potential role of adenosine A2A receptor antagonists in the treatment of movement disorders
    • Mally, J., and Stone, T. W. (1998) Potential role of adenosine A2A receptor antagonists in the treatment of movement disorders. CNS Drugs 10, 311-320.
    • (1998) CNS Drugs , vol.10 , pp. 311-320
    • Mally, J.1    Stone, T.W.2
  • 26
    • 0031594271 scopus 로고    scopus 로고
    • Adenosine A2A antagonist: A novel antiparkinsonian agent that does not provoke dyskinesia in parkinsonian monkeys
    • Kanda, T., Jackson, M. J., Smith, L. A., Pearce, R. K., Nakamura, J., Kase, H., Kuwana, Y., and Jenner, P. (1998) Adenosine A2A antagonist: a novel antiparkinsonian agent that does not provoke dyskinesia in parkinsonian monkeys. Ann. Neurol. 43, 507-513.
    • (1998) Ann. Neurol. , vol.43 , pp. 507-513
    • Kanda, T.1    Jackson, M.J.2    Smith, L.A.3    Pearce, R.K.4    Nakamura, J.5    Kase, H.6    Kuwana, Y.7    Jenner, P.8
  • 27
    • 0344052684 scopus 로고    scopus 로고
    • Antiparkinsonian effect of a new selective adenosine A2A receptor antagonist in MPTP-treatedmonkeys
    • Grondin, R., Bedard, P. J., Hadj Tahar, A., Gregoire, L., Mori, A., and Kase, H. (1999) Antiparkinsonian effect of a new selective adenosine A2A receptor antagonist in MPTP-treatedmonkeys. Neurol. 52, 1673-1677.
    • (1999) Neurol , vol.52 , pp. 1673-1677
    • Grondin, R.1    Bedard, P.J.2    Hadj Tahar, A.3    Gregoire, L.4    Mori, A.5    Kase, H.6
  • 28
    • 0036020950 scopus 로고    scopus 로고
    • Neuroprotection by adenosine A2A receptor blockade in experimental models of Parkinson's disease
    • Ikeda, K., Kurokawa, M., Aoyama, S., and Kuwana, Y. (2002) Neuroprotection by adenosine A2A receptor blockade in experimental models of Parkinson's disease. J. Neurochem. 80, 262-270.
    • (2002) J. Neurochem. , vol.80 , pp. 262-270
    • Ikeda, K.1    Kurokawa, M.2    Aoyama, S.3    Kuwana, Y.4
  • 29
    • 0021810979 scopus 로고
    • Inhibition of NADH-linked oxidation in brain mitochondria by 1-methyl-4-phenylpyridine, a metabolite of the neurotoxin, 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine
    • Nicklas, W. J., Vyas, I., and Heikkila, R. E. (1985) Inhibition of NADH-linked oxidation in brain mitochondria by 1-methyl-4-phenylpyridine, a metabolite of the neurotoxin, 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine. Life Sci. 36, 2503-2538.
    • (1985) Life Sci. , vol.36 , pp. 2503-2538
    • Nicklas, W.J.1    Vyas, I.2    Heikkila, R.E.3
  • 30
    • 0022515585 scopus 로고
    • Inhibition of mitochondrial NADH dehydrogenase by pyridine derivatives and its possible relation to experimental and idiopathic parkinsonism
    • Ramsay, R. R., Salach, J. I., and Singer, T. P. (1986) Inhibition of mitochondrial NADH dehydrogenase by pyridine derivatives and its possible relation to experimental and idiopathic parkinsonism. Biochem. Biophys. Res. Commun. 134, 743-748.
    • (1986) Biochem. Biophys. Res. Commun. , vol.134 , pp. 743-748
    • Ramsay, R.R.1    Salach, J.I.2    Singer, T.P.3
  • 32
    • 19944428678 scopus 로고    scopus 로고
    • A1 adenosine receptor antagonists, 3-aryl[1,2,4]triazino[4,3-α]benzimidazol-4-(10H)- ones (ATBIs) and N-alkyl and N-acyl-(7-substituted-2-phenylimidazo- [1,2-α][1,3,5]triazin-4-yl)amines (ITAs): Different recognition of bovine and human binding sites
    • Da Settimo, F., Primofiore, G., Taliani, S., LaMotta, C., Novellino, E., Greco, G., Lavecchia, A., Cosimelli, B., Iadanza, M., Klotz, K.-N., Tuscano, D., Trincavelli, M. L., and Martini, C. (2004) A1 adenosine receptor antagonists, 3-aryl[1,2,4]triazino[4,3-α]benzimidazol-4-(10H)- ones (ATBIs) and N-alkyl and N-acyl-(7-substituted-2-phenylimidazo- [1,2-α][1,3,5]triazin-4-yl)amines (ITAs): Different recognition of bovine and human binding sites. Drug Dev. Res. 63, 1-7.
    • (2004) Drug Dev. Res. , vol.63 , pp. 1-7
    • Da Settimo, F.1    Primofiore, G.2    Taliani, S.3    Lamotta, C.4    Novellino, E.5    Greco, G.6    Lavecchia, A.7    Cosimelli, B.8    Iadanza, M.9    Klotz, K.-N.10    Tuscano, D.11    Trincavelli, M.L.12    Martini, C.13
  • 40
    • 0029127542 scopus 로고
    • The in vitro pharmacology of ZM 241385, a potent, non-xanthine A2a selective adenosine receptor antagonist
    • Poucher, S. M., Keddie, J. R., Singh, P., Stoggall, S. M., Caulkett, P. W., Jones, G., and Coll, M. G. (1995) The in vitro pharmacology of ZM 241385, a potent, non-xanthine A2a selective adenosine receptor antagonist. Br. J. Pharmacol. 115, 1096-1102.
    • (1995) Br. J. Pharmacol. , vol.115 , pp. 1096-1102
    • Poucher, S.M.1    Keddie, J.R.2    Singh, P.3    Stoggall, S.M.4    Caulkett, P.W.5    Jones, G.6    Coll, M.G.7
  • 41
    • 0025143320 scopus 로고
    • A modification of a protein-binding method for rapid quantification of cAMP in cell-culture supernatants and body fluid
    • Nordstedt, C., and Fredholm, B. B. (1990) A modification of a protein-binding method for rapid quantification of cAMP in cell-culture supernatants and body fluid. Anal. Biochem. 189, 231-234.
    • (1990) Anal. Biochem. , vol.189 , pp. 231-234
    • Nordstedt, C.1    Fredholm, B.B.2
  • 43
    • 0022272191 scopus 로고
    • Methamphetamine: Toxicity to dopaminergic neurons
    • Seiden, L. S. (1985) Methamphetamine: toxicity to dopaminergic neurons. NIDA Res. Monogr. 62, 100-116.
    • (1985) NIDA Res. Monogr. , vol.62 , pp. 100-116
    • Seiden, L.S.1
  • 45
    • 0034791072 scopus 로고    scopus 로고
    • Parallel increases in lipid and protein oxidative markers in several mouse brain regions after methamphetamine treatment
    • Gluck, M. R., Moy, L. Y., Jayatilleke, E., Hogan, K. A., Manzino, L., and Sonsalla, P. K. (2001) Parallel increases in lipid and protein oxidative markers in several mouse brain regions after methamphetamine treatment. J. Neurochem. 79, 152-160.
    • (2001) J. Neurochem. , vol.79 , pp. 152-160
    • Gluck, M.R.1    Moy, L.Y.2    Jayatilleke, E.3    Hogan, K.A.4    Manzino, L.5    Sonsalla, P.K.6
  • 46
    • 20144389039 scopus 로고    scopus 로고
    • Occurrence of neuronal inclusions combined with increased nigral expression of alpha-synuclein within dopaminergic neurons following treatment with amphetamine derivatives in mice
    • Fornai, F., Lenzi, P., Ferrucci, M., Lazzeri, G., di Poggio, A. B., Natale, G., Busceti, C. L., Biagioni, F., Giusiani, M., Ruggieri, S., and Paparelli, A. (2005) Occurrence of neuronal inclusions combined with increased nigral expression of alpha-synuclein within dopaminergic neurons following treatment with amphetamine derivatives in mice. Brain Res. Bull. 65, 405-413.
    • (2005) Brain Res. Bull. , vol.65 , pp. 405-413
    • Fornai, F.1    Lenzi, P.2    Ferrucci, M.3    Lazzeri, G.4    Di Poggio, A.B.5    Natale, G.6    Busceti, C.L.7    Biagioni, F.8    Giusiani, M.9    Ruggieri, S.10    Paparelli, A.11
  • 47
    • 33747141059 scopus 로고    scopus 로고
    • The neurotoxicity of amphetamines: Bridging drugs of abuse and neurodegenerative disorders
    • Iacovelli, L., Fulceri, F., De Blasi, A., Nicoletti, F., Ruggieri, S., and Fornai, F. (2006) The neurotoxicity of amphetamines: bridging drugs of abuse and neurodegenerative disorders. Exp. Neurol. 201, 24-31.
    • (2006) Exp. Neurol. , vol.201 , pp. 24-31
    • Iacovelli, L.1    Fulceri, F.2    De Blasi, A.3    Nicoletti, F.4    Ruggieri, S.5    Fornai, F.6
  • 52
    • 0033578032 scopus 로고    scopus 로고
    • Benzodiazepine receptor ligands. 4. Synthesis and pharmacological evaluation of 3-heteroaryl-8-chloropyrazolo[5,1-c][1,2,4] benzotriazine 5-oxides
    • Costanzo, A, Guerrini, G, Ciciani, G, Bruni, F, Selleri, S, Costa, B, Martini, C, Lucacchini, A, Aiello, P.M., and Ipponi, A. (1999) Benzodiazepine receptor ligands. 4. Synthesis and pharmacological evaluation of 3-heteroaryl-8-chloropyrazolo[5,1-c][1,2,4] benzotriazine 5-oxides. J. Med. Chem. 42 (12), 2218-2226.
    • (1999) J. Med. Chem. , vol.42 , Issue.12 , pp. 2218-2226
    • Costanzo, A.1    Guerrini, G.2    Ciciani, G.3    Bruni, F.4    Selleri, S.5    Costa, B.6    Martini, C.7    Lucacchini, A.8    Aiello, P.M.9    Ipponi, A.10
  • 54
    • 0024505521 scopus 로고
    • 1-aminocyclopropane carboxylic acid: A potent and selective ligand for the glycine modulatory site of the N-methyl-D-aspartate receptor complex
    • Marvizón, J. C., Lewin, A. H., and Skolnick, P. (1989) 1-Aminocyclopropane carboxylic acid: a potent and selective ligand for the glycine modulatory site of the N-methyl-D-aspartate receptor complex. J. Neurochem. 52 (3), 992-994.
    • (1989) J. Neurochem. , vol.52 , Issue.3 , pp. 992-994
    • Marvizón, J.C.1    Lewin, A.H.2    Skolnick, P.3
  • 55
    • 0015861774 scopus 로고
    • Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50% inhibition (I50) of an enzymatic reaction
    • Cheng, Y., and Prusoff, W. H. (1973) Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50% inhibition (I50) of an enzymatic reaction. Biochem. Pharmacol. 22, 3099-3108.
    • (1973) Biochem. Pharmacol. , vol.22 , pp. 3099-3108
    • Cheng, Y.1    Prusoff, W.H.2
  • 56
    • 37049191651 scopus 로고
    • A new procedure for staining vaginal smears
    • Papanicolau, G. N. (1942) A new procedure for staining vaginal smears. Science 95, 438-439.
    • (1942) Science , vol.95 , pp. 438-439
    • Papanicolau, G.N.1


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