메뉴 건너뛰기




Volumn 80, Issue , 2014, Pages 509-522

Anticonvulsant evaluation of clubbed indole-1,2,4-triazine derivatives: A synthetic approach

Author keywords

Anticonvulsant; GABA; Quantification; Sodium channel; Triazine

Indexed keywords

1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 2 PHENYL 5 (TRIFLUOROMETHYL) 1H INDOLE 3 CARBOXYLIC ACID; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 2 PHENYL 5 (TRIFLUOROMETHYL) 1H INDOLE 3 SULFONAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 (METHYLTHIO) 2 PHENYL 1H INDOLE 3 SULFONAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 CHLORO 2 PHENYL 1H INDOLE 3 CARBOXYLIC ACID; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 CHLORO 2 PHENYL 1H INDOLE 3 SULFONAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 FLUORO 2 PHENYL 1H INDOLE 3 CARBOXYLIC ACID; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 FLUORO 2 PHENYL 1H INDOLE 3 SULFONAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 METHOXY 2 PHENYL 1H INDOLE 3 CARBOXYLIC ACID; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 METHOXY 2 PHENYL 1H INDOLE 3 SULFONAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 NITRO 2 PHENYL 1H INDOLE 3 CARBOXAMIDE; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 NITRO 2 PHENYL 1H INDOLE 3 CARBOXYLIC ACID; 1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 NITRO 2 PHENYL 1H INDOLE 3 SULFONAMIDE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 2 PHENYL 5 (TRIFLUOROMETHYL) 1H INDOL 3 YL]ETHANONE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 (METHYLTHIO) 2 PHENYL 1H INDOL 3 YL]ETHANONE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 CHLORO 2 PHENYL 1H INDOL 3 YL]ETHANONE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 FLUORO 2 PHENYL 1H INDOL 3 YL]ETHANONE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 METHOXY 2 PHENYL 1H INDOL 3 YL]ETHANONE; 1 [1 (5 AMINO 3 THIOXO 2,3,4,5 TETRAHYDRO 1,2,4 TRIAZIN 6 YL) 5 NITRO 2 PHENYL 1H INDOL 3 YL]ETHANONE; 1,2,4 TRIAZINE DERIVATIVE; 4 AMINOBUTYRIC ACID; 6 (3 ALLYL 5 CHLORO 2 PHENYL 1H INDOL 1 YL) 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; 6 (3 ALLYL 5 FLUORO 2 PHENYL 1H INDOL 1 YL) 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; 6 (3 ALLYL 5 METHOXY 2 PHENYL 1H INDOL 1 YL) 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; 6 (3 ALLYL 5 NITRO 2 PHENYL 1H INDOL 1 YL) 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; 6 [3 ALLYL 2 PHENYL 5 (TRIFLUOROMETHYL) 1H INDOL 1 YL] 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; 6 [3 ALLYL 5 (METHYLTHIO) 2 PHENYL 1H INDOL 1 YL] 5 AMINO 4,5 DIHYDRO 1,2,4 TRIAZINE 3 (2H)THIONE; ANTICONVULSIVE AGENT; PENTETRAZOLE; SODIUM CHANNEL; UNCLASSIFIED DRUG; UNINDEXED DRUG; 1,2,4-TRIAZINE; TRIAZINE DERIVATIVE;

EID: 84899885782     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.04.043     Document Type: Article
Times cited : (69)

References (49)
  • 1
    • 84879807393 scopus 로고    scopus 로고
    • Design, synthesis and anticonvulsant evaluation of N-(benzo[d]thiazol-2- ylcarbamoyl)-2-methyl-4-oxoquinazoline-3(4H)-carbothioamide derivatives: A hybrid pharmacophore approach
    • S. Malik, R.S. Bahare, and S.A. Khan Design, synthesis and anticonvulsant evaluation of N-(benzo[d]thiazol-2-ylcarbamoyl)-2-methyl-4-oxoquinazoline-3(4H) -carbothioamide derivatives: a hybrid pharmacophore approach European Journal of Medicinal Chemistry 67 2013 1 13
    • (2013) European Journal of Medicinal Chemistry , vol.67 , pp. 1-13
    • Malik, S.1    Bahare, R.S.2    Khan, S.A.3
  • 3
    • 16344387731 scopus 로고    scopus 로고
    • Epileptic seizures and epilepsy: Definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE)
    • R.S. Fisher, W.E. Boas, W. Blume, C. Elger, P. Genton, P. Lee, and J. Engel Jr. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE) Epilepsia 46 2005 470 472
    • (2005) Epilepsia , vol.46 , pp. 470-472
    • Fisher, R.S.1    Boas, W.E.2    Blume, W.3    Elger, C.4    Genton, P.5    Lee, P.6    Engel, Jr.J.7
  • 4
    • 84899787162 scopus 로고    scopus 로고
    • Antiepileptic drugs currently in development, 19th World Congress of Neurology, Invited Abstracts
    • M. Brodie Antiepileptic drugs currently in development, 19th World Congress of Neurology, Invited Abstracts Journal of the Neurological Sciences 285 S1 2009 S5 S56
    • (2009) Journal of the Neurological Sciences , vol.285 , Issue.S1
    • Brodie, M.1
  • 6
    • 0034785484 scopus 로고    scopus 로고
    • Pharmacogenetics and antiepileptic drugs
    • B.B. Spear Pharmacogenetics and antiepileptic drugs Epilepsia 42 2001 31 34
    • (2001) Epilepsia , vol.42 , pp. 31-34
    • Spear, B.B.1
  • 7
    • 33646911656 scopus 로고    scopus 로고
    • New horizons in the development of antiepileptic drugs: Innovative strategies
    • W. Loscher, and D. Schmidt New horizons in the development of antiepileptic drugs: innovative strategies Epilepsy Research 69 2006 183 272
    • (2006) Epilepsy Research , vol.69 , pp. 183-272
    • Loscher, W.1    Schmidt, D.2
  • 8
    • 84873317261 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of bioisosteres of trimethadione, N-derivative-1,2,3-oxathiazolidine-4-one-2,2-dioxides from α-hydroxyamides
    • V. Pastore, L. Sabatier, A. Enrique, M. Marder, and L.E. Bruno-Blanch Synthesis and anticonvulsant activity of bioisosteres of trimethadione, N-derivative-1,2,3-oxathiazolidine-4-one-2,2-dioxides from α-hydroxyamides Bioorganic & Medicinal Chemistry 21 2013 841 846
    • (2013) Bioorganic & Medicinal Chemistry , vol.21 , pp. 841-846
    • Pastore, V.1    Sabatier, L.2    Enrique, A.3    Marder, M.4    Bruno-Blanch, L.E.5
  • 9
    • 84880462938 scopus 로고    scopus 로고
    • Design of innovative therapeutics for pharmacoresistant epilepsy: Challenges and needs
    • D.F. Weaver Design of innovative therapeutics for pharmacoresistant epilepsy: challenges and needs Epilepsia 54 2013 56 59
    • (2013) Epilepsia , vol.54 , pp. 56-59
    • Weaver, D.F.1
  • 11
    • 67349117806 scopus 로고    scopus 로고
    • Drug treatment of epilepsy: Options and limitations
    • D. Schmidt Drug treatment of epilepsy: options and limitations Epilepsy Behavior 15 2009 56 65
    • (2009) Epilepsy Behavior , vol.15 , pp. 56-65
    • Schmidt, D.1
  • 12
    • 0024997911 scopus 로고
    • Established anticonvulsants and treatment of refractory epilepsy
    • M.J. Brodie Established anticonvulsants and treatment of refractory epilepsy Lancet 336 1990 350 354
    • (1990) Lancet , vol.336 , pp. 350-354
    • Brodie, M.J.1
  • 13
    • 0024449997 scopus 로고
    • Animal models of the epilepsies
    • R.S. Fisher Animal models of the epilepsies Brain Research Reviews 14 1989 245 278
    • (1989) Brain Research Reviews , vol.14 , pp. 245-278
    • Fisher, R.S.1
  • 14
    • 80955137560 scopus 로고    scopus 로고
    • Design, synthesis and antiepileptic properties of novel 1-(substituted-benzylidene)-3-(1-(morpholino/piperidino-methyl)-2, 3-dioxoindolin-5-yl) urea derivatives
    • C.R. Prakash, and S. Raja Design, synthesis and antiepileptic properties of novel 1-(substituted-benzylidene)-3-(1-(morpholino/piperidino-methyl)-2,3- dioxoindolin-5-yl) urea derivatives European Journal of Medicinal Chemistry 46 2011 6057 6065
    • (2011) European Journal of Medicinal Chemistry , vol.46 , pp. 6057-6065
    • Prakash, C.R.1    Raja, S.2
  • 15
    • 0036347772 scopus 로고    scopus 로고
    • Animal models of epilepsy for the development of antiepileptogenic and disease-modifying drugs. A comparison of the pharmacology of kindling and post-status epilepticus models of temporal lobe epilepsy
    • W. Loscher Animal models of epilepsy for the development of antiepileptogenic and disease-modifying drugs. A comparison of the pharmacology of kindling and post-status epilepticus models of temporal lobe epilepsy Epilepsy Research 50 2002 105 123
    • (2002) Epilepsy Research , vol.50 , pp. 105-123
    • Loscher, W.1
  • 17
    • 33846917985 scopus 로고    scopus 로고
    • Syntheses and anti-cancer activities of 2-[1-(indol-3-yl-/pyrimidin-5-yl/ pyridine-2-yl-/quinolin-2-yl)-but-3-enylamino]-2-phenyl-ethanols
    • P. Singh, P. Kaur, V. Luxami, S. Kaur, and S. Kumar Syntheses and anti-cancer activities of 2-[1-(indol-3-yl-/pyrimidin-5-yl/pyridine-2-yl-/ quinolin-2-yl)-but-3-enylamino]-2-phenyl-ethanols Bioorganic & Medicinal Chemistry 15 2007 2386 2395
    • (2007) Bioorganic & Medicinal Chemistry , vol.15 , pp. 2386-2395
    • Singh, P.1    Kaur, P.2    Luxami, V.3    Kaur, S.4    Kumar, S.5
  • 20
    • 54049095612 scopus 로고    scopus 로고
    • Thiazolyl/oxazolyl formazanyl indoles as potent anti-inflammatory agents
    • N. Singh, S.K. Bhati, and A. Kumar Thiazolyl/oxazolyl formazanyl indoles as potent anti-inflammatory agents European Journal of Medicinal Chemistry 43 2008 2597 2609
    • (2008) European Journal of Medicinal Chemistry , vol.43 , pp. 2597-2609
    • Singh, N.1    Bhati, S.K.2    Kumar, A.3
  • 22
    • 64049092267 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors. The nematode α-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3- substituted-phenyl-1H-indole-5-sulfonamides
    • O. Guzel, A. Innocenti, R.A. Hall, A. Scozzafava, F.A. Mühlschlegel, and C.T. Supuran Carbonic anhydrase inhibitors. The nematode α-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides Bioorganic & Medicinal Chemistry 17 2009 3212 3215
    • (2009) Bioorganic & Medicinal Chemistry , vol.17 , pp. 3212-3215
    • Guzel, O.1    Innocenti, A.2    Hall, R.A.3    Scozzafava, A.4    Mühlschlegel, F.A.5    Supuran, C.T.6
  • 23
    • 0023038693 scopus 로고
    • The effect of lamotrigine, a novel anticonvulsant, on interictal spikes in patients with epilepsy
    • S. Jawad, J. Oxley, W.C. Yuen, and A. Richens The effect of lamotrigine, a novel anticonvulsant, on interictal spikes in patients with epilepsy British Journal of Clinical Pharmacology 22 1986 191 193
    • (1986) British Journal of Clinical Pharmacology , vol.22 , pp. 191-193
    • Jawad, S.1    Oxley, J.2    Yuen, W.C.3    Richens, A.4
  • 25
    • 75149197657 scopus 로고    scopus 로고
    • Bioactivation of lamotrigine in vivo in rat and in vitro in human liver microsomes, hepatocytes, and epidermal keratinocytes: Characterization of thioether conjugates by liquid chromatography/mass spectrometry and high field nuclear magnetic resonance spectroscopy
    • H. Chen, S. Grover, L. Yu, G. Walker, and A. Mutlib Bioactivation of lamotrigine in vivo in rat and in vitro in human liver microsomes, hepatocytes, and epidermal keratinocytes: characterization of thioether conjugates by liquid chromatography/mass spectrometry and high field nuclear magnetic resonance spectroscopy Chemical Research in Toxicology 23 2010 159 170
    • (2010) Chemical Research in Toxicology , vol.23 , pp. 159-170
    • Chen, H.1    Grover, S.2    Yu, L.3    Walker, G.4    Mutlib, A.5
  • 26
    • 80053004364 scopus 로고    scopus 로고
    • Structural Alert/Reactive metabolite concept as applied in medicinal chemistry to mitigate the risk of idiosyncratic drug toxicity: A perspective based on the critical examination of trends in the top 200 drugs marketed in the United States
    • A.F. Stepan, D.P. Walker, J. Bauman, D.A. Price, T.A. Baillie, A.S. Kalgutkar, and M.D. Aleo Structural Alert/Reactive metabolite concept as applied in medicinal chemistry to mitigate the risk of idiosyncratic drug toxicity: a perspective based on the critical examination of trends in the top 200 drugs marketed in the United States Chemical Research in Toxicology 24 2011 1345 1410
    • (2011) Chemical Research in Toxicology , vol.24 , pp. 1345-1410
    • Stepan, A.F.1    Walker, D.P.2    Bauman, J.3    Price, D.A.4    Baillie, T.A.5    Kalgutkar, A.S.6    Aleo, M.D.7
  • 27
    • 77957223212 scopus 로고    scopus 로고
    • Molecular model of anticonvulsant drug binding to the voltage-gated sodium channel inner pore
    • G.M. Lipkind, and H.A. Fozzard Molecular model of anticonvulsant drug binding to the voltage-gated sodium channel inner pore Molecular Pharmacology 78 2010 631 638
    • (2010) Molecular Pharmacology , vol.78 , pp. 631-638
    • Lipkind, G.M.1    Fozzard, H.A.2
  • 29
    • 84873292163 scopus 로고    scopus 로고
    • Probing the steric requirements of the γ-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin
    • J.I. Juncosa Jr., A.P. Groves, G. Xia, and R.B. Silverman Probing the steric requirements of the γ-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin Bioorganic & Medicinal Chemistry 21 2013 903 911
    • (2013) Bioorganic & Medicinal Chemistry , vol.21 , pp. 903-911
    • Juncosa, Jr.J.I.1    Groves, A.P.2    Xia, G.3    Silverman, R.B.4
  • 30
    • 84862858037 scopus 로고    scopus 로고
    • Chemical properties of antiepileptic drugs (AEDs)
    • M. Bialer Chemical properties of antiepileptic drugs (AEDs) Advanced Drug Delivery Reviews 64 2012 887 895
    • (2012) Advanced Drug Delivery Reviews , vol.64 , pp. 887-895
    • Bialer, M.1
  • 31
    • 79955685813 scopus 로고    scopus 로고
    • Combining antiepileptic drugs - Rational polytherapy
    • M.J. Brodie, and G.J. Sills Combining antiepileptic drugs - Rational polytherapy Seizure 20 2011 369 375
    • (2011) Seizure , vol.20 , pp. 369-375
    • Brodie, M.J.1    Sills, G.J.2
  • 33
    • 0024208020 scopus 로고
    • Anticonvulsant hypersensitivity syndrome in vitro assessment of risk
    • N.H. Shear, and S.P. Spielberg Anticonvulsant hypersensitivity syndrome in vitro assessment of risk The Journal of Clinical Investigation 82 1988 1826 1832
    • (1988) The Journal of Clinical Investigation , vol.82 , pp. 1826-1832
    • Shear, N.H.1    Spielberg, S.P.2
  • 34
    • 0035848570 scopus 로고    scopus 로고
    • Mapping and fitting the peripheral benzodiazepine receptor binding site by carboxamide derivatives. Comparison of different approaches to quantitative ligand-receptor interaction modeling
    • M. Anzini, A. Cappelli, S. Vomero, M. Seeber, and M. Cristina Mapping and fitting the peripheral benzodiazepine receptor binding site by carboxamide derivatives. Comparison of different approaches to quantitative ligand-receptor interaction modeling Journal of Medicinal Chemistry 44 2001 1134 1150
    • (2001) Journal of Medicinal Chemistry , vol.44 , pp. 1134-1150
    • Anzini, M.1    Cappelli, A.2    Vomero, S.3    Seeber, M.4    Cristina, M.5
  • 35
    • 0029053795 scopus 로고
    • Evaluation of the semicarbazones, thiosemicarbazones and bis-carbohydrazones of some aryl alicycylic ketones for anticonvulsant and other biological properties
    • J.R. Dimmock, S.C. Vashishtha, and J.P. Stables Evaluation of the semicarbazones, thiosemicarbazones and bis-carbohydrazones of some aryl alicycylic ketones for anticonvulsant and other biological properties European Journal of Medicinal Chemistry 30 1995 303 314
    • (1995) European Journal of Medicinal Chemistry , vol.30 , pp. 303-314
    • Dimmock, J.R.1    Vashishtha, S.C.2    Stables, J.P.3
  • 36
    • 0033748227 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones
    • S.N. Pandeya, P. Yogeswari, and J.P. Stables Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones European Journal of Medicinal Chemistry 35 2000 879 886
    • (2000) European Journal of Medicinal Chemistry , vol.35 , pp. 879-886
    • Pandeya, S.N.1    Yogeswari, P.2    Stables, J.P.3
  • 41
    • 70449177837 scopus 로고
    • A note on a simple apparatus for detecting neurological deficit in rats and mice
    • N.W. Dunham, and T.A. Miya A note on a simple apparatus for detecting neurological deficit in rats and mice Journal of the American Pharmaceutical Association 46 1957 208 209
    • (1957) Journal of the American Pharmaceutical Association , vol.46 , pp. 208-209
    • Dunham, N.W.1    Miya, T.A.2
  • 42
    • 33644982586 scopus 로고    scopus 로고
    • 2,4-Dimethoxyphenyl semicarbazones with anticonvulsant activity against three animal models of seizure: Synthesis and pharmacological evaluation
    • R. Thirumurugan, D. Sriram, A. Saxena, J.P. Stables, and P. Yogeeswari 2,4-Dimethoxyphenyl semicarbazones with anticonvulsant activity against three animal models of seizure: synthesis and pharmacological evaluation Bioorganic & Medicinal Chemistry 14 2006 3106 3112
    • (2006) Bioorganic & Medicinal Chemistry , vol.14 , pp. 3106-3112
    • Thirumurugan, R.1    Sriram, D.2    Saxena, A.3    Stables, J.P.4    Yogeeswari, P.5
  • 43
    • 84879817537 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of dialkyl 4-(benzo[d][1,3]dioxol-6-yl)- 1,4-dihydro-2,6-dimethyl-1-substituted-pyridine-3,5-dicarboxylates as potential anticonvulsants and their molecular properties prediction
    • G. Prasanthi, K.V.S.R.G. Prasad, and K. Bharathi Design, synthesis and evaluation of dialkyl 4-(benzo[d][1,3]dioxol-6-yl)-1,4-dihydro-2,6-dimethyl-1- substituted-pyridine-3,5-dicarboxylates as potential anticonvulsants and their molecular properties prediction European Journal of Medicinal Chemistry 66 2013 516 525
    • (2013) European Journal of Medicinal Chemistry , vol.66 , pp. 516-525
    • Prasanthi, G.1    Prasad, K.V.S.R.G.2    Bharathi, K.3
  • 45
    • 34548165281 scopus 로고    scopus 로고
    • Timed pentylenetetrazol infusion test: A comparative analysis with s.c.PTZ and MES models of anticonvulsant screening in mice
    • S.N. Mandhane, K. Aavula, and T. Rajamannar Timed pentylenetetrazol infusion test: a comparative analysis with s.c.PTZ and MES models of anticonvulsant screening in mice Seizure 16 2007 636 644
    • (2007) Seizure , vol.16 , pp. 636-644
    • Mandhane, S.N.1    Aavula, K.2    Rajamannar, T.3
  • 49
    • 0023691172 scopus 로고
    • Anticonvulsant activities of phenyl-substituted bicyclic 2,4-oxazolidinediones and monocyclic models. Comparison with binding to the neuronal voltage-dependent sodium channel
    • W.J. Brouillette, G.B. Brown, T.M. DeLorey, S.S. Shirali, and G.L. Grunewald Anticonvulsant activities of phenyl-substituted bicyclic 2,4-oxazolidinediones and monocyclic models. Comparison with binding to the neuronal voltage-dependent sodium channel Journal of Medicinal Chemistry 31 1988 2218 2221
    • (1988) Journal of Medicinal Chemistry , vol.31 , pp. 2218-2221
    • Brouillette, W.J.1    Brown, G.B.2    Delorey, T.M.3    Shirali, S.S.4    Grunewald, G.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.