-
1
-
-
0032914455
-
Antagonists selective for NMDA receptors containing the NR2B subunit
-
Chenard, B. L. and Menniti, F. S. (1999) Antagonists selective for NMDA receptors containing the NR2B subunit Curr. Pharm. Des. 5, 381-404 (Pubitemid 29238998)
-
(1999)
Current Pharmaceutical Design
, vol.5
, Issue.5
, pp. 381-404
-
-
Chenard, B.L.1
Menniti, F.S.2
-
2
-
-
0035577313
-
NMDA receptor antagonists as analgesics: Focus on the NR2B subtype
-
DOI 10.1016/S0165-6147(00)01863-0, PII S0165614700018630
-
Chizh, B. A., Headley, P. M., and Tzschentke, T. M. (2001) NMDA receptor antagonists as analgesics: Focus on the NR2B subtype Trends Pharmacol. Sci. 22, 636-642 (Pubitemid 33135525)
-
(2001)
Trends in Pharmacological Sciences
, vol.22
, Issue.12
, pp. 636-642
-
-
Chizh, B.A.1
Headley P.Max2
Tzschentke, T.M.3
-
3
-
-
0031443289
-
Ro 25-6981, a highly potent and selective blocker of N-methyl-D- aspartate receptors containing the NR2B subunit. Characterization in vitro
-
Fischer, G., Mutel, V., Trube, G., Malherbe, P., Kew, J. N., Mohacsi, E., Heitz, M. P., and Kemp, J. A. (1997) Ro 25-6981, a highly potent and selective blocker of N-methyl- d -aspartate receptors containing the NR2B subunit. Characterization in vitro J. Pharmacol. Exp. Ther. 283, 1285-1292 (Pubitemid 28016504)
-
(1997)
Journal of Pharmacology and Experimental Therapeutics
, vol.283
, Issue.3
, pp. 1285-1292
-
-
Fischer, G.1
Mutel, V.2
Trube, G.3
Malherbe, P.4
Kew, J.N.C.5
Mohacsi, E.6
Heitz, M.P.7
Kemp, J.A.8
-
4
-
-
0036720776
-
Pharmacological characterization of Ro 63-1908 (1-[2-(4-hydroxy-phenoxy)- ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a novel subtype-selective N-methyl-D-aspartate antagonist
-
DOI 10.1124/jpet.102.034322
-
Gill, R., Alanine, A., Bourson, A., Buttelmann, B., Fischer, G., Heitz, M. P., Kew, J. N., Levet-Trafit, B., Lorez, H. P., Malherbe, P., Miss, M. T., Mutel, V., Pinard, E., Roever, S., Schmitt, M., Trube, G., Wybrecht, R., Wyler, R., and Kemp, J. A. (2002) Pharmacological characterization of Ro 63-1908 (1-[2-(4-hydroxy-phenoxy)-ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a novel subtype-selective N-methyl- d -aspartate antagonist J. Pharmacol. Exp. Ther. 302, 940-948 (Pubitemid 34920214)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.302
, Issue.3
, pp. 940-948
-
-
Gill, R.1
Alanine, A.2
Bourson, A.3
Buttelmann, B.4
Fischer, G.5
Heitz, M.-P.6
Kew, J.N.C.7
Levet-Trafit, B.8
Lorez, H.-P.9
Malherbe, P.10
Miss, M.-T.11
Mutel, V.12
Pinard, E.13
Roever, S.14
Schmitt, M.15
Trube, G.16
Wybrecht, R.17
Wyler, R.18
Kemp, J.A.19
-
5
-
-
77955365676
-
Quinazolin-4-one derivatives: A novel class of noncompetitive NR2C/D subunit-selective N-methyl- d -aspartate receptor antagonists
-
Mosley, C. A., Acker, T. M., Hansen, K. B., Mullasseril, P., Andersen, K. T., Le, P., Vellano, K. M., Brauner-Osborne, H., Liotta, D. C., and Traynelis, S. F. (2010) Quinazolin-4-one derivatives: A novel class of noncompetitive NR2C/D subunit-selective N-methyl- d -aspartate receptor antagonists J. Med. Chem. 53, 5476-5490
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5476-5490
-
-
Mosley, C.A.1
Acker, T.M.2
Hansen, K.B.3
Mullasseril, P.4
Andersen, K.T.5
Le, P.6
Vellano, K.M.7
Brauner-Osborne, H.8
Liotta, D.C.9
Traynelis, S.F.10
-
6
-
-
68649104759
-
Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl- d -aspartate receptors
-
Mosley, C. A., Myers, S. J., Murray, E. E., Santangelo, R., Tahirovic, Y. A., Kurtkaya, N., Mullasseril, P., Yuan, H., Lyuboslavsky, P., Le, P., Wilson, L. J., Yepes, M., Dingledine, R., Traynelis, S. F., and Liotta, D. C. (2009) Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl- d -aspartate receptors Bioorg. Med. Chem. 17, 6463-6480
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6463-6480
-
-
Mosley, C.A.1
Myers, S.J.2
Murray, E.E.3
Santangelo, R.4
Tahirovic, Y.A.5
Kurtkaya, N.6
Mullasseril, P.7
Yuan, H.8
Lyuboslavsky, P.9
Le, P.10
Wilson, L.J.11
Yepes, M.12
Dingledine, R.13
Traynelis, S.F.14
Liotta, D.C.15
-
7
-
-
70350452578
-
N-Methyl- d -aspartate (NMDA) receptor NR2 subunit selectivity of a series of novel piperazine-2,3-dicarboxylate derivatives: Preferential blockade of extrasynaptic NMDA receptors in the rat hippocampal CA3-CA1 synapse
-
Costa, B. M., Feng, B., Tsintsadze, T. S., Morley, R. M., Irvine, M. W., Tsintsadze, V., Lozovaya, N. A., Jane, D. E., and Monaghan, D. T. (2009) N-Methyl- d -aspartate (NMDA) receptor NR2 subunit selectivity of a series of novel piperazine-2,3-dicarboxylate derivatives: Preferential blockade of extrasynaptic NMDA receptors in the rat hippocampal CA3-CA1 synapse J. Pharmacol. Exp. Ther. 331, 618-626
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.331
, pp. 618-626
-
-
Costa, B.M.1
Feng, B.2
Tsintsadze, T.S.3
Morley, R.M.4
Irvine, M.W.5
Tsintsadze, V.6
Lozovaya, N.A.7
Jane, D.E.8
Monaghan, D.T.9
-
8
-
-
1542269774
-
Structure - Activity analysis of a novel NR2C/NR2D-preferring NMDA receptor antagonist: 1-(phenanthrene-2-carbonyl) piperazine-2,3-dicarboxylic acid
-
DOI 10.1038/sj.bjp.0705644
-
Feng, B., Tse, H. W., Skifter, D. A., Morley, R., Jane, D. E., and Monaghan, D. T. (2004) Structure-activity analysis of a novel NR2C/NR2D-preferring NMDA receptor antagonist: 1-(Phenanthrene-2-carbonyl) piperazine-2,3-dicarboxylic acid Br. J. Pharmacol. 141, 508-516 (Pubitemid 38297013)
-
(2004)
British Journal of Pharmacology
, vol.141
, Issue.3
, pp. 508-516
-
-
Feng, B.1
Tse, H.W.2
Skifter, D.A.3
Morley, R.4
Jane, D.E.5
Monaghan, D.T.6
-
9
-
-
19444366505
-
Identification of subunit- and antagonist-specific amino acid residues in the N-methyl-D-aspartate receptor glutamate-binding pocket
-
DOI 10.1124/jpet.104.082990
-
Kinarsky, L., Feng, B., Skifter, D. A., Morley, R. M., Sherman, S., Jane, D. E., and Monaghan, D. T. (2005) Identification of subunit- and antagonist-specific amino acid residues in the N-methyl- d -aspartate receptor glutamate-binding pocket J. Pharmacol. Exp. Ther. 313, 1066-1074 (Pubitemid 40727010)
-
(2005)
Journal of Pharmacology and Experimental Therapeutics
, vol.313
, Issue.3
, pp. 1066-1074
-
-
Kinarsky, L.1
Feng, B.2
Skifter, D.A.3
Morley, R.M.4
Sherman, S.5
Jane, D.E.6
Monaghan, D.T.7
-
10
-
-
17144378207
-
1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists
-
DOI 10.1021/jm0492498
-
Morley, R. M., Tse, H. W., Feng, B., Miller, J. C., Monaghan, D. T., and Jane, D. E. (2005) Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists J. Med. Chem. 48, 2627-2637 (Pubitemid 40516452)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2627-2637
-
-
Morley, R.M.1
Tse, H.-W.2
Feng, B.3
Miller, J.C.4
Monaghan, D.T.5
Jane, D.E.6
-
11
-
-
0032478159
-
5-Aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists
-
DOI 10.1016/S0960-894X(98)00055-9, PII S0960894X98000559
-
Acklin, P., Allgeier, H., Auberson, Y. P., Bischoff, S., Ofner, S., Sauer, D., and Schmutz, M. (1998) 5-Aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists Bioorg. Med. Chem. Lett. 8, 493-498 (Pubitemid 28092381)
-
(1998)
Bioorganic and Medicinal Chemistry Letters
, vol.8
, Issue.5
, pp. 493-498
-
-
Acklin, P.1
Allgeier, H.2
Auberson, Y.P.3
Bischoff, S.4
Ofner, S.5
Sauer, D.6
Schmutz, M.7
-
12
-
-
0034598310
-
Synthesis, radiolabelling and biological characterization of (D)-7-iodo- N-(1-phosphonoethyl)-5-aminomethylquinoxaline-2,3-dione, a glycine-binding site antagonist of NMDA receptors
-
DOI 10.1016/S0960-894X(99)00576-4, PII S0960894X99005764
-
Ametamey, S. M., Kokic, M., Carrey-Remy, N., Blauenstein, P., Willmann, M., Bischoff, S., Schmutz, M., Schubiger, P. A., and Auberson, Y. P. (2000) Synthesis, radiolabelling and biological characterization of d -7-iodo-N-(1-phosphonoethyl)-5-aminomethylquinoxaline-2,3-dione, a glycine-binding site antagonist of NMDA receptors Bioorg. Med. Chem. Lett. 10, 75-78 (Pubitemid 30014675)
-
(2000)
Bioorganic and Medicinal Chemistry Letters
, vol.10
, Issue.1
, pp. 75-78
-
-
Ametamey, S.M.1
Kokic, M.2
Carrey-Remy, N.3
Blauenstein, P.4
Willmann, M.5
Bischoff, S.6
Schmutz, M.7
Schubiger, P.A.8
Auberson, Y.P.9
-
13
-
-
0033579923
-
N-phosphonoalkyl-5-aminomethylquinoxaline-2,3-diones: In vivo active AMPA and NMDA(glycine) antagonists
-
DOI 10.1016/S0960-894X(98)00720-3, PII S0960894X98007203
-
Auberson, Y. P., Acklin, P., Bischoff, S., Moretti, R., Ofner, S., Schmutz, M., and Veenstra, S. J. (1999) N-Phosphonoalkyl-5- aminomethylquinoxaline-2,3-diones: In vivo active AMPA and NMDA(glycine) antagonists Bioorg. Med. Chem. Lett. 9, 249-254 (Pubitemid 29059539)
-
(1999)
Bioorganic and Medicinal Chemistry Letters
, vol.9
, Issue.2
, pp. 249-254
-
-
Auberson, Y.P.1
Acklin, P.2
Bischoff, S.3
Moretti, R.4
Ofner, S.5
Schmutz, M.6
Veenstra, S.J.7
-
14
-
-
0037041183
-
5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition
-
DOI 10.1016/S0960-894X(02)00074-4, PII S0960894X02000744
-
Auberson, Y. P., Allgeier, H., Bischoff, S., Lingenhoehl, K., Moretti, R., and Schmutz, M. (2002) 5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition Bioorg. Med. Chem. Lett. 12, 1099-1102 (Pubitemid 34242811)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.7
, pp. 1099-1102
-
-
Auberson, Y.P.1
Allgeier, H.2
Bischoff, S.3
Lingenhoehl, K.4
Moretti, R.5
Schmutz, M.6
-
15
-
-
9144236304
-
Conantokins: Peptide antagonists of NMDA receptors
-
Layer, R. T., Wagstaff, J. D., and White, H. S. (2004) Conantokins: Peptide antagonists of NMDA receptors Curr. Med. Chem. 11, 3073-3084 (Pubitemid 39545576)
-
(2004)
Current Medicinal Chemistry
, vol.11
, Issue.23
, pp. 3073-3084
-
-
Layer, R.T.1
Wagstaff, J.D.2
White, H.S.3
-
16
-
-
34249010244
-
The molecular basis of Conantokin antagonism of NMDA receptor function
-
DOI 10.2174/138945007780618481
-
Prorok, M. and Castellino, F. J. (2007) The molecular basis of conantokin antagonism of NMDA receptor function Curr. Drug Targets 8, 633-642 (Pubitemid 46785061)
-
(2007)
Current Drug Targets
, vol.8
, Issue.5
, pp. 633-642
-
-
Prorok, M.1
Castellino, F.J.2
-
17
-
-
0033851790
-
Conantokin G is an NR2B-selective competitive antagonist of N-methyl- d -aspartate receptors
-
Donevan, S. D. and McCabe, R. T. (2000) Conantokin G is an NR2B-selective competitive antagonist of N-methyl- d -aspartate receptors Mol. Pharmacol. 58, 614-623
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 614-623
-
-
Donevan, S.D.1
McCabe, R.T.2
-
18
-
-
34547211472
-
Subtype-selective antagonism of N-methyl-d-aspartate receptor ion channels by synthetic conantokin peptides
-
DOI 10.1016/j.neuropharm.2007.04.016, PII S0028390807001244
-
Sheng, Z., Dai, Q., Prorok, M., and Castellino, F. J. (2007) Subtype-selective antagonism of N-methyl- d -aspartate receptor ion channels by synthetic conantokin peptides Neuropharmacology 53, 145-156 (Pubitemid 47125955)
-
(2007)
Neuropharmacology
, vol.53
, Issue.1
, pp. 145-156
-
-
Sheng, Z.1
Dai, Q.2
Prorok, M.3
Castellino, F.J.4
-
19
-
-
67650125196
-
The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B
-
Sheng, Z., Liang, Z., Geiger, J. H., Prorok, M., and Castellino, F. J. (2009) The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B Neuropharmacology 57, 127-136
-
(2009)
Neuropharmacology
, vol.57
, pp. 127-136
-
-
Sheng, Z.1
Liang, Z.2
Geiger, J.H.3
Prorok, M.4
Castellino, F.J.5
-
20
-
-
79953236709
-
Specific determinants of conantokins that dictate their selectivity for the NR2B subunit of N-methyl- d -aspartate receptors
-
Sheng, Z., Prorok, M., and Castellino, F. J. (2010) Specific determinants of conantokins that dictate their selectivity for the NR2B subunit of N-methyl- d -aspartate receptors Neuroscience 170, 703-710
-
(2010)
Neuroscience
, vol.170
, pp. 703-710
-
-
Sheng, Z.1
Prorok, M.2
Castellino, F.J.3
-
21
-
-
62149122662
-
Neuroprotective and cardioprotective conopeptides: An emerging class of drug leads
-
Twede, V. D., Miljanich, G., Olivera, B. M., and Bulaj, G. (2009) Neuroprotective and cardioprotective conopeptides: An emerging class of drug leads Curr. Opin. Drug Discovery Dev. 12, 231-239
-
(2009)
Curr. Opin. Drug Discovery Dev.
, vol.12
, pp. 231-239
-
-
Twede, V.D.1
Miljanich, G.2
Olivera, B.M.3
Bulaj, G.4
-
22
-
-
66149126942
-
Conantokin-Br from Conus brettinghami and selectivity determinants for the NR2D subunit of the NMDA receptor
-
Twede, V. D., Teichert, R. W., Walker, C. S., Gruszczynski, P., Kazmierkiewicz, R., Bulaj, G., and Olivera, B. M. (2009) Conantokin-Br from Conus brettinghami and selectivity determinants for the NR2D subunit of the NMDA receptor Biochemistry 48, 4063-4073
-
(2009)
Biochemistry
, vol.48
, pp. 4063-4073
-
-
Twede, V.D.1
Teichert, R.W.2
Walker, C.S.3
Gruszczynski, P.4
Kazmierkiewicz, R.5
Bulaj, G.6
Olivera, B.M.7
-
23
-
-
56349135882
-
NR2B-selective conantokin peptide inhibitors of the NMDA receptor display enhanced antinociceptive properties compared to non-selective conantokins
-
Xiao, C., Huang, Y., Dong, M., Hu, J., Hou, S., Castellino, F. J., Prorok, M., and Dai, Q. (2008) NR2B-selective conantokin peptide inhibitors of the NMDA receptor display enhanced antinociceptive properties compared to non-selective conantokins Neuropeptides 42, 601-609
-
(2008)
Neuropeptides
, vol.42
, pp. 601-609
-
-
Xiao, C.1
Huang, Y.2
Dong, M.3
Hu, J.4
Hou, S.5
Castellino, F.J.6
Prorok, M.7
Dai, Q.8
-
24
-
-
0037219288
-
Powerful antinociceptive effects of the cone snail venom-derived subtype-selective NMDA receptor antagonists conantokins G and T
-
DOI 10.1016/S0304-3959(02)00303-2
-
Malmberg, A. B., Gilbert, H., McCabe, R. T., and Basbaum, A. I. (2003) Powerful antinociceptive effects of the cone snail venom-derived subtype-selective NMDA receptor antagonists conantokins G and T Pain 101, 109-116 (Pubitemid 36044658)
-
(2003)
Pain
, vol.101
, Issue.1-2
, pp. 109-116
-
-
Malmberg, A.B.1
Gilbert, H.2
McCabe, R.T.3
Basbaum, A.I.4
-
25
-
-
58549085757
-
Antinociceptive effects of the marine snail peptides conantokin-G and conotoxin MVIIA alone and in combination in rat models of pain
-
Hama, A. and Sagen, J. (2009) Antinociceptive effects of the marine snail peptides conantokin-G and conotoxin MVIIA alone and in combination in rat models of pain Neuropharmacology 56, 556-563
-
(2009)
Neuropharmacology
, vol.56
, pp. 556-563
-
-
Hama, A.1
Sagen, J.2
-
26
-
-
2342649960
-
The effect of CGX-1007 and CI-1041, novel NMDA receptor antagonists, on NMDA receptor-mediated EPSCs
-
DOI 10.1016/j.eplepsyres.2003.12.011, PII S0920121104000506
-
Barton, M. E., White, H. S., and Wilcox, K. S. (2004) The effect of CGX-1007 and CI-1041, novel NMDA receptor antagonists, on NMDA receptor-mediated EPSCs Epilepsy Res. 59, 13-24 (Pubitemid 38595417)
-
(2004)
Epilepsy Research
, vol.59
, Issue.1
, pp. 13-24
-
-
Barton, M.E.1
White, H.S.2
Wilcox, K.S.3
-
27
-
-
0036146487
-
New antiepileptic drugs currently in clinical trials: Is there a strategy in their development?
-
DOI 10.1097/00007691-200202000-00015
-
Bialer, M. (2002) New antiepileptic drugs currently in clinical trials: Is there a strategy in their development? Ther. Drug Monit. 24, 85-90 (Pubitemid 34106737)
-
(2002)
Therapeutic Drug Monitoring
, vol.24
, Issue.1
, pp. 85-90
-
-
Bialer, M.1
-
28
-
-
0036752811
-
Progress report on new antiepileptic drugs: A summary of the Sixth Eilat Conference (EILAT VI)
-
DOI 10.1016/S0920-1211(02)00106-7, PII S0920121102001067
-
Bialer, M., Johannessen, S. I., Kupferberg, H. J., Levy, R. H., Loiseau, P., and Perucca, E. (2002) Progress report on new antiepileptic drugs: A summary of the Sixth Eilat Conference (EILAT VI) Epilepsy Res. 51, 31-71 (Pubitemid 35283878)
-
(2002)
Epilepsy Research
, vol.51
, Issue.1-2
, pp. 31-71
-
-
Bialer, M.1
Johannessen, S.I.2
Kupferberg, H.J.3
Levy, R.H.4
Loiseau, P.5
Perucca, E.6
-
29
-
-
52949118506
-
Conus Venoms: A Rich Source of Peptide-Based Therapeutics
-
Han, T. S., Teichert, R. W., Olivera, B. M., and Bulaj, G. (2008) Conus Venoms: A Rich Source of Peptide-Based Therapeutics Curr. Pharm. Des. 14, 2462-2479
-
(2008)
Curr. Pharm. Des.
, vol.14
, pp. 2462-2479
-
-
Han, T.S.1
Teichert, R.W.2
Olivera, B.M.3
Bulaj, G.4
-
30
-
-
33845992556
-
Conus peptides: Biodiversity-based discovery and exogenomics
-
DOI 10.1074/jbc.R600020200
-
Olivera, B. M. (2006) Conus peptides: Biodiversity-based discovery and exogenomics J. Biol. Chem. 281, 31173-31177 (Pubitemid 46041381)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.42
, pp. 31173-31177
-
-
Olivera, B.M.1
-
31
-
-
77953391048
-
Natural products and ion channel pharmacology
-
Teichert, R. W. and Olivera, B. M. (2010) Natural products and ion channel pharmacology Future Med. Chem. 2, 731-744
-
(2010)
Future Med. Chem.
, vol.2
, pp. 731-744
-
-
Teichert, R.W.1
Olivera, B.M.2
-
32
-
-
2342444944
-
The A-superfamily of conotoxins: Structural and functional divergence
-
DOI 10.1074/jbc.M309654200
-
Santos, A. D., McIntosh, J. M., Hillyard, D. R., Cruz, L. J., and Olivera, B. M. (2004) The A-superfamily of conotoxins: Structural and functional divergence J. Biol. Chem. 279, 17596-17606 (Pubitemid 38560524)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.17
, pp. 17596-17606
-
-
Santos, A.D.1
McIntosh, J.M.2
Hillyard, D.R.3
Cruz, L.J.4
Olivera, B.M.5
-
33
-
-
50449088156
-
Integrating the discovery pipeline for novel compounds targeting ion channels
-
Bulaj, G. (2008) Integrating the discovery pipeline for novel compounds targeting ion channels Curr. Opin. Chem. Biol. 12, 441-447
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 441-447
-
-
Bulaj, G.1
-
34
-
-
37549069739
-
Novel Conantokins from Conus parius Venom Are Specific Antagonists of N-Methyl- d -aspartate Receptors
-
Teichert, R. W., Jimenez, E. C., Twede, V., Watkins, M., Hollmann, M., Bulaj, G., and Olivera, B. M. (2007) Novel Conantokins from Conus parius Venom Are Specific Antagonists of N-Methyl- d -aspartate Receptors J. Biol. Chem. 282, 36905-36913
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 36905-36913
-
-
Teichert, R.W.1
Jimenez, E.C.2
Twede, V.3
Watkins, M.4
Hollmann, M.5
Bulaj, G.6
Olivera, B.M.7
-
35
-
-
49449100631
-
Conantokin-P, an Unusual Conantokin with a Long Disulfide Loop
-
Gowd, K. H., Twede, V., Watkins, M., Krishnanb, K. S., Teichert, R. W., Bulaj, G., and Olivera, B. M. (2008) Conantokin-P, an Unusual Conantokin with a Long Disulfide Loop Toxicon 52, 203-213
-
(2008)
Toxicon
, vol.52
, pp. 203-213
-
-
Gowd, K.H.1
Twede, V.2
Watkins, M.3
Krishnanb, K.S.4
Teichert, R.W.5
Bulaj, G.6
Olivera, B.M.7
-
36
-
-
77957300637
-
Characterization of conantokin Rl-A: Molecular phylogeny as structure/function study
-
Gowd, K. H., Watkins, M., Twede, V. D., Bulaj, G. W., and Olivera, B. M. (2010) Characterization of conantokin Rl-A: Molecular phylogeny as structure/function study J. Pept. Sci. 16, 375-382
-
(2010)
J. Pept. Sci.
, vol.16
, pp. 375-382
-
-
Gowd, K.H.1
Watkins, M.2
Twede, V.D.3
Bulaj, G.W.4
Olivera, B.M.5
-
37
-
-
0028169661
-
Ligand affinities at recombinant N-methyl- d -aspartate receptors depend on subunit composition
-
Laurie, D. J. and Seeburg, P. H. (1994) Ligand affinities at recombinant N-methyl- d -aspartate receptors depend on subunit composition Eur. J. Pharmacol. 268, 335-345
-
(1994)
Eur. J. Pharmacol.
, vol.268
, pp. 335-345
-
-
Laurie, D.J.1
Seeburg, P.H.2
-
38
-
-
0028226884
-
Regional and developmental heterogeneity in splicing of the rat brain NMDAR1 mRNA
-
Laurie, D. J. and Seeburg, P. H. (1994) Regional and developmental heterogeneity in splicing of the rat brain NMDAR1 mRNA J. Neurosci. 14, 3180-3194 (Pubitemid 24139002)
-
(1994)
Journal of Neuroscience
, vol.14
, Issue.5
, pp. 3180-3194
-
-
Laurie, D.J.1
Seeburg, P.H.2
-
39
-
-
0035920125
-
The amino acid residue at sequence position 5 in the conantokin peptides partially governs subunit-selective antagonism of recombinant N-methyl- d -aspartate receptors
-
Klein, R. C., Prorok, M., Galdzicki, Z., and Castellino, F. J. (2001) The amino acid residue at sequence position 5 in the conantokin peptides partially governs subunit-selective antagonism of recombinant N-methyl- d -aspartate receptors J. Biol. Chem. 276, 26860-26867
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 26860-26867
-
-
Klein, R.C.1
Prorok, M.2
Galdzicki, Z.3
Castellino, F.J.4
-
40
-
-
0034783460
-
Kinetic and mechanistic characterization of NMDA receptor antagonism by replacement and truncation variants of the conantokin peptides
-
DOI 10.1016/S0028-3908(01)00119-8, PII S0028390801001198
-
Klein, R. C., Warder, S. E., Galdzicki, Z., Castellino, F. J., and Prorok, M. (2001) Kinetic and mechanistic characterization of NMDA receptor antagonism by replacement and truncation variants of the conantokin peptides Neuropharmacology 41, 801-810 (Pubitemid 33001414)
-
(2001)
Neuropharmacology
, vol.41
, Issue.7
, pp. 801-810
-
-
Klein, R.C.1
Warder, S.E.2
Galdzicki, Z.3
Castellino, F.J.4
Prorok, M.5
-
41
-
-
58149089158
-
Design, synthesis, and characterization of high-affinity, systemically-active galanin analogues with potent anticonvulsant activities
-
Bulaj, G., Green, B. R., Lee, H. K., Robertson, C. R., White, K., Zhang, L., Sochanska, M., Flynn, S. P., Scholl, E. A., Pruess, T. H., Smith, M. D., and White, H. S. (2008) Design, synthesis, and characterization of high-affinity, systemically-active galanin analogues with potent anticonvulsant activities J. Med. Chem. 51, 8038-8047
-
(2008)
J. Med. Chem.
, vol.51
, pp. 8038-8047
-
-
Bulaj, G.1
Green, B.R.2
Lee, H.K.3
Robertson, C.R.4
White, K.5
Zhang, L.6
Sochanska, M.7
Flynn, S.P.8
Scholl, E.A.9
Pruess, T.H.10
Smith, M.D.11
White, H.S.12
-
42
-
-
0037074985
-
Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits
-
Chatterton, J. E., Awobuluyi, M., Premkumar, L. S., Takahashi, H., Talantova, M., Shin, Y., Cui, J., Tu, S., Sevarino, K. A., Nakanishi, N., Tong, G., Lipton, S. A., and Zhang, D. (2002) Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits Nature 415, 793-798 (Pubitemid 34150501)
-
(2002)
Nature
, vol.415
, Issue.6873
, pp. 793-798
-
-
Chatterton, J.E.1
Awobuluyi, M.2
Premkumar, L.S.3
Takahashi, H.4
Talantova, M.5
Shin, Y.6
Cul, J.7
Tu, S.8
Sevarino, K.A.9
Nakanishi, N.10
Tong, G.11
Lipton, S.A.12
Zhang, D.13
-
43
-
-
0030449042
-
Calcium binding properties of synthetic γ-carboxyglutamic acid-containing marine cone snail "sleeper" peptides, conantokin-G and conantokin-T
-
Prorok, M., Warder, S. E., Blandl, T., and Castellino, F. J. (1996) Calcium binding properties of synthetic γ-carboxyglutamic acid-containing marine cone snail "sleeper" peptides, conantokin-G and conantokin-T Biochemistry 35, 16528-16534
-
(1996)
Biochemistry
, vol.35
, pp. 16528-16534
-
-
Prorok, M.1
Warder, S.E.2
Blandl, T.3
Castellino, F.J.4
-
44
-
-
0032797897
-
Calcium binding mode of gamma-carboxyglutamic acids in conantokins
-
Lin, C. H., Chan, F. C., Hwang, J. K., and Lyu, P. C. (1999) Calcium binding mode of γ-carboxyglutamic acids in conantokins Protein Eng. 12, 589-595 (Pubitemid 29368966)
-
(1999)
Protein Engineering
, vol.12
, Issue.7
, pp. 589-595
-
-
Lin, C.H.1
Chan, F.C.H.2
Hwang, J.K.3
Lyu, P.C.4
-
45
-
-
0031456675
-
Role of gamma-carboxyglutamic acid in the calcium-induced structural transition of conantokin G, a conotoxin from the marine snail Conus geographus
-
DOI 10.1021/bi9718550
-
Rigby, A. C., Baleja, J. D., Li, L., Pedersen, L. G., Furie, B. C., and Furie, B. (1997) Role of γ-carboxyglutamic acid in the calcium-induced structural transition of conantokin G, a conotoxin from the marine snail Conus geographus Biochemistry 36, 15677-15684 (Pubitemid 28027366)
-
(1997)
Biochemistry
, vol.36
, Issue.50
, pp. 15677-15684
-
-
Rigby, A.C.1
Baleja, J.D.2
Li, L.3
Pedersen, L.G.4
Furie, B.C.5
Furie, B.6
-
46
-
-
0032568831
-
Conformational changes in conantokin-G induced upon binding of calcium and magnesium as revealed by NMR structural analysis
-
DOI 10.1074/jbc.273.26.16248
-
Chen, Z., Blandl, T., Prorok, M., Warder, S. E., Li, L., Zhu, Y., Pedersen, L. G., Ni, F., and Castellino, F. J. (1998) Conformational changes in conantokin-G induced upon binding of calcium and magnesium as revealed by NMR structural analysis J. Biol. Chem. 273, 16248-16258 (Pubitemid 28311401)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.26
, pp. 16248-16258
-
-
Chen, Z.1
Blandl, T.2
Prorok, M.3
Warder, S.E.4
Li, L.5
Zhu, Y.6
Pedersen, L.G.7
Ni, F.8
Castellino, F.J.9
-
47
-
-
33846961465
-
The crystal structures of the calcium-bound con-G and con-T[K7γ] dimeric peptides demonstrate a metal-dependent helix-forming motif
-
Cnudde, S. E., Prorok, M., Dai, Q., Castellino, F. J., and Geiger, J. H. (2007) The crystal structures of the calcium-bound con-G and con-T[K7γ] dimeric peptides demonstrate a metal-dependent helix-forming motif J. Am. Chem. Soc. 129, 1586-1593
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1586-1593
-
-
Cnudde, S.E.1
Prorok, M.2
Dai, Q.3
Castellino, F.J.4
Geiger, J.H.5
-
48
-
-
0034798601
-
Point mutations identify the glutamate binding pocket of the N-methyl-D-aspartate receptor as major site of Conantokin-G inhibition
-
DOI 10.1016/S0028-3908(01)00112-5, PII S0028390801001125
-
Wittekindt, B., Malany, S., Schemm, R., Otvos, L., Maccecchini, M. L., Laube, B., and Betz, H. (2001) Point mutations identify the glutamate binding pocket of the N-methyl- d -aspartate receptor as major site of conantokin-G inhibition Neuropharmacology 41, 753-761 (Pubitemid 32972193)
-
(2001)
Neuropharmacology
, vol.41
, Issue.6
, pp. 753-761
-
-
Wittekindt, B.1
Malany, S.2
Schemm, R.3
Otvos, L.4
Maccecchini, M.-L.5
Laube, B.6
Betz, H.7
-
49
-
-
79955099725
-
CGX-1007 prevents excitotoxic cell death via actions at multiple types of NMDA receptors
-
Alex, A. B., Saunders, G. W., Dalpe-Charron, A., Reilly, C. A., and Wilcox, K. S. (2011) CGX-1007 prevents excitotoxic cell death via actions at multiple types of NMDA receptors Neurotoxicology 32, 392-399
-
(2011)
Neurotoxicology
, vol.32
, pp. 392-399
-
-
Alex, A.B.1
Saunders, G.W.2
Dalpe-Charron, A.3
Reilly, C.A.4
Wilcox, K.S.5
-
50
-
-
33644837888
-
NMDA receptor subunit-dependent modulation by conantokin-G and Ala7-conantokin-G
-
Ragnarsson, L., Yasuda, T., Lewis, R. J., Dodd, P. R., and Adams, D. J. (2006) NMDA receptor subunit-dependent modulation by conantokin-G and Ala7-conantokin-G J. Neurochem. 96, 283-291
-
(2006)
J. Neurochem.
, vol.96
, pp. 283-291
-
-
Ragnarsson, L.1
Yasuda, T.2
Lewis, R.J.3
Dodd, P.R.4
Adams, D.J.5
-
51
-
-
0021684624
-
γ-Carboxyglutamate in a neuroactive toxin
-
McIntosh, J. M., Olivera, B. M., Cruz, L. J., and Gray, W. R. (1984) γ-Carboxyglutamate in a neuroactive toxin J. Biol. Chem. 259, 14343-14346
-
(1984)
J. Biol. Chem.
, vol.259
, pp. 14343-14346
-
-
McIntosh, J.M.1
Olivera, B.M.2
Cruz, L.J.3
Gray, W.R.4
-
52
-
-
0025241893
-
γ-carboxyglutamate containing peptide with N-methyl- d -aspartate antagonist activity
-
Haack, J. A., Rivier, J., Parks, T. N., Mena, E. E., Cruz, L. J., and Olivera, B. M. (1990) Conantokin-T. A γ-carboxyglutamate containing peptide with N-methyl- d -aspartate antagonist activity J. Biol. Chem. 265, 6025-6029
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 6025-6029
-
-
Haack, J.A.1
Rivier, J.2
Parks, T.N.3
Mena, E.E.4
Cruz, L.J.5
Olivera, B.M.6
Conantokin, A.-T.7
-
53
-
-
0033976427
-
In vitro and in vivo characterization of conantokin-R, a selective NMDA receptor antagonist isolated from the venom of the fish-hunting snail Conus radiatus
-
White, H. S., McCabe, R. T., Armstrong, H., Donevan, S. D., Cruz, L. J., Abogadie, F. C., Torres, J., Rivier, J. E., Paarmann, I., Hollmann, M., and Olivera, B. M. (2000) In vitro and in vivo characterization of conantokin-R, a selective NMDA receptor antagonist isolated from the venom of the fish-hunting snail Conus radiatus J. Pharmacol. Exp. Ther. 292, 425-432 (Pubitemid 30026402)
-
(2000)
Journal of Pharmacology and Experimental Therapeutics
, vol.292
, Issue.1
, pp. 425-432
-
-
White, H.S.1
McCabe, R.T.2
Armstrong, H.3
Donevan, S.D.4
Cruz, L.J.5
Abogadie, F.C.6
Torres, J.7
Rivier, J.E.8
Paarmann, I.9
Hollmann, M.10
Olivera, B.M.11
-
54
-
-
0036753261
-
Conantokin-L, a new NMDA receptor antagonist: Determinants for anticonvulsant potency
-
DOI 10.1016/S0920-1211(02)00101-8, PII S0920121102001018
-
Jimenez, E. C., Donevan, S., Walker, C., Zhou, L. M., Nielsen, J., Cruz, L. J., Armstrong, H., White, H. S., and Olivera, B. M. (2002) Conantokin-L, a new NMDA receptor antagonist: Determinants for anticonvulsant potency Epilepsy Res. 51, 73-80 (Pubitemid 35283879)
-
(2002)
Epilepsy Research
, vol.51
, Issue.1-2
, pp. 73-80
-
-
Jimenez, E.C.1
Donevan, S.2
Walker, C.3
Zhou, L.-M.4
Nielsen, J.5
Cruz, L.J.6
Armstrong, H.7
White H.Steve8
Olivera, B.M.9
-
55
-
-
49449100631
-
Conantokin-P, an unusual conantokin with a long disulfide loop
-
Gowd, K. H., Twede, V., Watkins, M., Krishnan, K. S., Teichert, R. W., Bulaj, G., and Olivera, B. M. (2008) Conantokin-P, an unusual conantokin with a long disulfide loop Toxicon 52, 203-213
-
(2008)
Toxicon
, vol.52
, pp. 203-213
-
-
Gowd, K.H.1
Twede, V.2
Watkins, M.3
Krishnan, K.S.4
Teichert, R.W.5
Bulaj, G.6
Olivera, B.M.7
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