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Volumn 9, Issue 10, 2012, Pages 891-898

Novel non-competitive antagonists of kainate GluK1/GluK2 receptors

Author keywords

Allosteric modulators; Glutamate receptors; Indole derivatives; Kainate receptors; Molecular modelling, Non competitive antagonists of kainate receptors

Indexed keywords

1 [(4 CHLOROPHENYL)METHYL] 5 METHOXY 2 (4 METHOXYPHENYL) 3 METHYLINDOLE; 1 ETHYL 2 (4 METHOXYPHENYL) 3 METHYLINDOLE; 1 ETHYL 2 PHENYL 5 METHOXY 3 METHYLINDOLE; 1 ETHYL 5 METHOXY 2 (4 METHOXYPHENYL) 3 METHYLINDOLE; 1 ETHYL 5 METHOXY 2 PHENYLINDOLE; 11 ETHYL 8 METHOXY 6,11 DIHYDRO 5H BENZO[A]CARBAZOLE; 5 METHOXY 2 (4 METHOXYPHENYL) 3 METHYLINDOLE; CALCIUM ION; GLUK1 RECEPTOR; GLUK2 RECEPTOR; GLUTAMATE RECEPTOR; INDOLE DERIVATIVE; ION CHANNEL; KAINIC ACID; KAINIC ACID RECEPTOR; KAINIC ACID RECEPTOR ANTAGONIST; UNCLASSIFIED DRUG;

EID: 84870419172     PISSN: 15701808     EISSN: 1875628X     Source Type: Journal    
DOI: 10.2174/157018012804586978     Document Type: Article
Times cited : (9)

References (24)
  • 1
    • 77955599312 scopus 로고    scopus 로고
    • Molecular structure of ionotropic glutamate receptors
    • Kaczor, A.A.; Matosiuk, D. Molecular structure of ionotropic glutamate receptors. Curr. Med. Chem., 2010, 17(24), 2608-2635.
    • (2010) Curr. Med. Chem. , vol.17 , Issue.24 , pp. 2608-2635
    • Kaczor, A.A.1    Matosiuk, D.2
  • 2
    • 67049133178 scopus 로고    scopus 로고
    • New antiepileptic drugs: Molecular targets
    • Mula, M. New antiepileptic drugs: molecular targets. Cent. Nerv. Syst. Agents Med. Chem., 2009, 9(2), 79-86.
    • (2009) Cent. Nerv. Syst. Agents Med. Chem. , vol.9 , Issue.2 , pp. 79-86
    • Mula, M.1
  • 3
    • 77955984700 scopus 로고    scopus 로고
    • Using glutamate homeostasis as a target for treating addictive disorders
    • Reissner, K.J.; Kalivas, P.W. Using glutamate homeostasis as a target for treating addictive disorders. Behav. Pharmacol., 2010, 21(5-6), 514-522.
    • (2010) Behav. Pharmacol. , vol.21 , Issue.5-6 , pp. 514-522
    • Reissner, K.J.1    Kalivas, P.W.2
  • 4
    • 84855927044 scopus 로고    scopus 로고
    • Targeting glutamate synapses in schizophrenia
    • Field, J.R.; Walker, A.G.; Conn, P.J. Targeting glutamate synapses in schizophrenia. Trends Mol. Med., 2011, 17(12), 689-698.
    • (2011) Trends Mol. Med. , vol.17 , Issue.12 , pp. 689-698
    • Field, J.R.1    Walker, A.G.2    Conn, P.J.3
  • 5
    • 48849113877 scopus 로고    scopus 로고
    • Ionotropic glutamate receptors & CNS disorders
    • Bowie, D. Ionotropic glutamate receptors & CNS disorders. CNS Neurol. Disord. Drug Targets, 2008, 7(2), 129-143.
    • (2008) CNS Neurol. Disord. Drug Targets , vol.7 , Issue.2 , pp. 129-143
    • Bowie, D.1
  • 6
    • 79952245139 scopus 로고    scopus 로고
    • Kainate receptors coming of age: Milestones of two decades of research
    • Contractor, A.; Mulle, C.; Swanson, G.T. Kainate receptors coming of age: milestones of two decades of research. Trends Neurosci., 2011, 34(3), 154-163.
    • (2011) Trends Neurosci. , vol.34 , Issue.3 , pp. 154-163
    • Contractor, A.1    Mulle, C.2    Swanson, G.T.3
  • 7
    • 0346365496 scopus 로고    scopus 로고
    • 2-Arylureidobenzoic Acids: Selective noncompetitive antagonists for the homomeric kainate receptor subtype GluR5
    • DOI 10.1021/jm030428j
    • Valgeirsson, J.; Nielsen, E. Ø. Peters, D.; Varming, T.; Mathiesen, C.; Kristensen, A. S.; Madsen, U. 2-arylureidobenzoic acids: selective noncompetitive antagonists for the homomeric kainate receptor subtype GluR5. J. Med. Chem., 2003, 46(26), 5834-5843. (Pubitemid 37547967)
    • (2003) Journal of Medicinal Chemistry , vol.46 , Issue.26 , pp. 5834-5843
    • Valgeirsson, J.1    Nielsen, E.O.2    Peters, D.3    Varming, T.4    Mathiesen, C.5    Kristensen, A.S.6    Madsen, U.7
  • 8
    • 11244334171 scopus 로고    scopus 로고
    • Bioisosteric modifications of 2-arylureidobenzoic acids: Selective noncompetitive antagonists for the homomeric kainate receptor subtype GluR5
    • DOI 10.1021/jm030638w
    • Valgeirsson, J.; Nielsen, E. Ø. Peters, D.; Mathiesen, C.; Kristensen, A. S.; Madsen, U. Bioisosteric modifications of 2-arylureidobenzoic acids: selective noncompetitive antagonists for the homomeric kainate receptor subtype GluR5. J. Med. Chem., 2004, 47(27), 6948-6957. (Pubitemid 40063595)
    • (2004) Journal of Medicinal Chemistry , vol.47 , Issue.27 , pp. 6948-6957
    • Valgeirsson, J.1    Nielsen, E.O.2    Peters, D.3    Mathiesen, C.4    Kristensen, A.S.5    Madsen, U.6
  • 12
    • 0021738560 scopus 로고
    • 2-Phenylindoles. Relationship between structure, estrogen receptor affinity, and mammary tumor inhibiting activity in the rat
    • DOI 10.1021/jm00377a011
    • von Angerer, E.; Prekajac, J.; Strohmeier, J. 2-Phenylindoles. Relationship between structure, estrogen receptor affinity, and mammary tumor inhibiting activity in the rat. J. Med. Chem., 1984, 27(11), 1439-1447. (Pubitemid 15200565)
    • (1984) Journal of Medicinal Chemistry , vol.27 , Issue.11 , pp. 1439-1447
    • Von Angerer, E.1    Prekajac, J.2    Strohmeier, J.3
  • 13
    • 0023078836 scopus 로고
    • 2-Phenylindoles. Effect of Nbenzylation on estrogen receptor affinity, estrogenic properties, and mammary tumor inhibiting activity
    • von Angerer, E.; Strohmeier, J. 2-Phenylindoles. Effect of Nbenzylation on estrogen receptor affinity, estrogenic properties, and mammary tumor inhibiting activity. J. Med. Chem., 1987, 30(1), 131-1366.
    • (1987) J. Med. Chem. , vol.30 , Issue.1 , pp. 131-1366
    • Von Angerer, E.1    Strohmeier, J.2
  • 14
    • 0024988751 scopus 로고
    • 1-(Aminoalkyl)-2-phenylindoles as novel pure estrogen antagonists
    • DOI 10.1021/jm00171a045
    • Von Angerer, E.; Knebel, N.; Kager, M.; Ganss, B. 1-(aminoalkyl)-2- phenylindoles as novel pure estrogen antagonists. J. Med. Chem., 1990, 33(9), 2635-2640. (Pubitemid 20274225)
    • (1990) Journal of Medicinal Chemistry , vol.33 , Issue.9 , pp. 2635-2640
    • Von Angerer, E.1    Knebel, N.2    Kager, M.3    Ganss, B.4
  • 15
    • 0025815056 scopus 로고
    • 2-Phenylindole-linked [2-(aminoalkyl)pyridine]dichloroplatinum(II): Complexes with a selective action on estrogen receptor positive mammary tumors
    • Knebel, N.G.; von Angerer, E. 2-Phenylindole-linked [2-(aminoalkyl) pyridine]dichloroplatinum(II): complexes with a selective action on estrogen receptor positive mammary tumors. J. Med. Chem., 1991, 34(7), 2145-2152.
    • (1991) J. Med. Chem. , vol.34 , Issue.7 , pp. 2145-2152
    • Knebel, N.G.1    Von Angerer, E.2
  • 16
    • 0036979174 scopus 로고    scopus 로고
    • Sulfamoyloxy-substituted 2-phenylindoles: Antiestrogen-based inhibitors of the steroid sulfatase in human breast cancer cells
    • DOI 10.1016/S0968-0896(02)00306-1, PII S0968089602003061
    • Golob, T.; Liebl, R.; von Angerer, E. Sulfamoyloxy-substituted 2-phenylindoles: antiestrogen-based inhibitors of the steroid sulfatase in human breast cancer cells. Bioorg. Med. Chem., 2002, 10(12):3941-3953. (Pubitemid 36164693)
    • (2002) Bioorganic and Medicinal Chemistry , vol.10 , Issue.12 , pp. 3941-3953
    • Golob, T.1    Liebl, R.2    Von Angerer, E.3
  • 17
    • 57749086723 scopus 로고    scopus 로고
    • Tethered indoles as functionalizable ligands for the estrogen receptor
    • Trogden, B.G.; Kim, S.H.; Lee, S.; Katzenellenbogen, J.A. Tethered indoles as functionalizable ligands for the estrogen receptor. Bioorg. Med. Chem. Lett., 2009, 19(2):485-488.
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , Issue.2 , pp. 485-488
    • Trogden, B.G.1    Kim, S.H.2    Lee, S.3    Katzenellenbogen, J.A.4
  • 18
    • 33947482239 scopus 로고
    • The Fisher indole synthesis
    • Robinson, B. The Fisher indole synthesis. Chem. Rev., 1963, 63(4), 373-401.
    • (1963) Chem. Rev. , vol.63 , Issue.4 , pp. 373-401
    • Robinson, B.1
  • 19
    • 0032481002 scopus 로고    scopus 로고
    • Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerization
    • DOI 10.1021/jm980228l
    • Gastpar, R.; Goldbrunner, M.; Marko, D.; von Angerer, E. Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerization. J. Med. Chem., 1998, 41(25), 4965-4972. (Pubitemid 28555455)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.25 , pp. 4965-4972
    • Gastpar, R.1    Goldbrunner, M.2    Marko, D.3    Von Angerer, E.4
  • 20
    • 46849101059 scopus 로고    scopus 로고
    • Theoretical studies on the structure and symmetry of the transmembrane region of glutamatergic GluR5 receptor
    • DOI 10.1021/jm7011694
    • Kaczor, A.A.; Kijkowska-Murak, U.A.; Matosiuk, D. Theoretical studies on the structure and symmetry of the transmembrane region of glutamatergic GluR5 receptor. J. Med. Chem., 2008, 51(13), 3765-3776. (Pubitemid 351956508)
    • (2008) Journal of Medicinal Chemistry , vol.51 , Issue.13 , pp. 3765-3776
    • Kaczor, A.A.1    Kijkowska-Murak, U.A.2    Matosiuk, D.3
  • 21
    • 66149186986 scopus 로고    scopus 로고
    • Modeling of glutamate GluR6 receptor and its interactions with novel noncompetitive antagonists
    • Kaczor, A.A.; Kijkowska-Murak, U.A.; Kronbach, C.; Unverferth, K.; Matosiuk, D. Modeling of glutamate GluR6 receptor and its interactions with novel noncompetitive antagonists. J. Chem. Inf. Model. 2009, 49(4), 1094-1104.
    • (2009) J. Chem. Inf. Model. , vol.49 , Issue.4 , pp. 1094-1104
    • Kaczor, A.A.1    Kijkowska-Murak, U.A.2    Kronbach, C.3    Unverferth, K.4    Matosiuk, D.5
  • 23
    • 84869023958 scopus 로고    scopus 로고
    • Wavefunction, Inc.
    • Spartan10, Wavefunction, Inc., http://www.wavefun.com.
    • Spartan10
  • 24
    • 4043162793 scopus 로고    scopus 로고
    • VEGA - An open platform to develop chemo-bio-informatics applications, using plug-in architecture and script programming
    • DOI 10.1023/B:JCAM.0000035186.90683.f2
    • Pedretti, A.; Villa, L.; Vistoli, G. VEGA -an open platform to develop chemo-bio-informatic applications, using plug-in architecture and script" programming. J. Comput. Aided Mol. Des. 2004, 18(3), 167-173. (Pubitemid 39069412)
    • (2004) Journal of Computer-Aided Molecular Design , vol.18 , Issue.3 , pp. 167-173
    • Pedretti, A.1    Villa, L.2    Vistoli, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.