-
1
-
-
37849001772
-
Electrostatic contributions of aromatic residues in the local anesthetic receptor of voltage-gated sodium channels
-
Ahern, C. A., Eastwood, A. L., Dougherty, D. A., and Horn, R. (2008). Electrostatic contributions of aromatic residues in the local anesthetic receptor of voltage-gated sodium channels. Circ. Res. 102, 86-94.
-
(2008)
Circ. Res
, vol.102
, pp. 86-94
-
-
Ahern, C.A.1
Eastwood, A.L.2
Dougherty, D.A.3
Horn, R.4
-
2
-
-
52949104364
-
Access and binding of local anesthetics in the closed sodium channel
-
Bruhova, I., Tikhonov, D. B., and Zhorov, B. S. (2008). Access and binding of local anesthetics in the closed sodium channel. Mol. Pharmacol. 74, 1033-1045.
-
(2008)
Mol. Pharmacol
, vol.74
, pp. 1033-1045
-
-
Bruhova, I.1
Tikhonov, D.B.2
Zhorov, B.S.3
-
3
-
-
77953504194
-
Hydroxylated analogs of mexiletine as tools for structural-requirements investigation of the sodium channel blocking activity
-
Catalano, A., Carocci, A., Cavalluzzi, M. M., Di Mola, A., Lentini, G., Lovece, A., Dipalma, A., Costanza, T., Desaphy, J.-F., Conte Camerino, D., and Franchini, C. (2010). Hydroxylated analogs of mexiletine as tools for structural-requirements investigation of the sodium channel blocking activity. Arch. Pharm. (Weinheim) 343, 325-332.
-
(2010)
Arch. Pharm. (Weinheim)
, vol.343
, pp. 325-332
-
-
Catalano, A.1
Carocci, A.2
Cavalluzzi, M.M.3
Di Mola, A.4
Lentini, G.5
Lovece, A.6
Dipalma, A.7
Costanza, T.8
Desaphy, J.-F.9
Conte Camerino, D.10
Franchini, C.11
-
4
-
-
1642498266
-
Stereospecific synthesis of "para-hydroxymexiletine" and sodium channel blocking activity evaluation
-
Catalano, A., Carocci, A., Fracchiolla, G., Franchini, C., Lentini, G., Tortorella, V., De Luca, A., De Bellis, M., Desaphy, J.-F., and Conte Camerino, D. (2004). Stereospecific synthesis of "para-hydroxymexiletine" and sodium channel blocking activity evaluation. Chirality 16, 72-78.
-
(2004)
Chirality
, vol.16
, pp. 72-78
-
-
Catalano, A.1
Carocci, A.2
Fracchiolla, G.3
Franchini, C.4
Lentini, G.5
Tortorella, V.6
De Luca, A.7
De Bellis, M.8
Desaphy, J.-F.9
Conte Camerino, D.10
-
5
-
-
35549010964
-
Synthesis of (R)-, (S)-, and (RS)hydroxymethylmexiletine, one of the major metabolites of mexiletine
-
Cavalluzzi, M. M., Catalano, A., Bruno, C., Lovece, A., Carocci, A., Corbo, F., Franchini, C., Lentini, G., and Tortorella, V. (2007). Synthesis of (R)-, (S)-, and (RS)hydroxymethylmexiletine, one of the major metabolites of mexiletine. Tetrahedron Asymmetry 18, 2409-2417.
-
(2007)
Tetrahedron Asymmetry
, vol.18
, pp. 2409-2417
-
-
Cavalluzzi, M.M.1
Catalano, A.2
Bruno, C.3
Lovece, A.4
Carocci, A.5
Corbo, F.6
Franchini, C.7
Lentini, G.8
Tortorella, V.9
-
6
-
-
33644877882
-
Systemic administration of local anesthetic agents to relieve neuropathic pain
-
Challapalli, V., Tremont-Lukats, I. W., McNicol, E. D., Lau, J., and Carr, D. B. (2005). Systemic administration of local anesthetic agents to relieve neuropathic pain. Cochrane Database Syst. Rev. 4, CD003345.
-
(2005)
Cochrane Database Syst. Rev
, vol.4
-
-
Challapalli, V.1
Tremont-Lukats, I.W.2
McNicol, E.D.3
Lau, J.4
Carr, D.B.5
-
7
-
-
33947512419
-
Ion channel pharmacology
-
Conte Camerino, D., Tricarico, D., and Desaphy, J.-F. (2007). Ion channel pharmacology. Neurotherapeutics 4, 184-198.
-
(2007)
Neurotherapeutics
, vol.4
, pp. 184-198
-
-
Conte Camerino, D.1
Tricarico, D.2
Desaphy, J.-F.3
-
8
-
-
33749018236
-
Evaluation of the pharmacological activity of the major mexiletine metabolites on skeletal muscle sodium currents
-
De Bellis, M., De Luca, A., Rana, F., Cavalluzzi, M. M., Catalano, A., Lentini, G., Franchini, C., Tortorella, V., and Conte Camerino, D. (2006). Evaluation of the pharmacological activity of the major mexiletine metabolites on skeletal muscle sodium currents. Br. J. Pharmacol. 149, 300-310.
-
(2006)
Br. J. Pharmacol
, vol.149
, pp. 300-310
-
-
De Bellis, M.1
De Luca, A.2
Rana, F.3
Cavalluzzi, M.M.4
Catalano, A.5
Lentini, G.6
Franchini, C.7
Tortorella, V.8
Conte Camerino, D.9
-
9
-
-
0033964620
-
Molecular determinants of mexiletine structure for potent and use-dependent block of skeletal muscle sodium channels
-
De Luca, A., Natuzzi, F., Desaphy, J.-F., Loni, G., Lentini, G., Franchini, C., Tortorella, V., and Conte Camerino, D. (2000). Molecular determinants of mexiletine structure for potent and use-dependent block of skeletal muscle sodium channels. Mol. Pharmacol. 57, 268-277.
-
(2000)
Mol. Pharmacol
, vol.57
, pp. 268-277
-
-
De Luca, A.1
Natuzzi, F.2
Desaphy, J.-F.3
Loni, G.4
Lentini, G.5
Franchini, C.6
Tortorella, V.7
Conte Camerino, D.8
-
10
-
-
2942701895
-
New potent mexiletine and tocainide analogues evaluated in vivo and in vitro as antimyotonic agents on myotonic ADR mouse
-
De Luca, A., Pierno, S., Liantonio, A., Desaphy, J.-F., Natuzzi, F., Didonna, M. P., Ferrannini, E., Jockusch, H., Franchini, C., Lentini, G., Corbo, F., Tortorella, V., and Conte Camerino, D. (2004). New potent mexiletine and tocainide analogues evaluated in vivo and in vitro as antimyotonic agents on myotonic ADR mouse. Neuromuscul. Disord. 14, 405-416.
-
(2004)
Neuromuscul. Disord
, vol.14
, pp. 405-416
-
-
De Luca, A.1
Pierno, S.2
Liantonio, A.3
Desaphy, J.-F.4
Natuzzi, F.5
Didonna, M.P.6
Ferrannini, E.7
Jockusch, H.8
Franchini, C.9
Lentini, G.10
Corbo, F.11
Tortorella, V.12
Conte Camerino, D.13
-
11
-
-
12444292787
-
Inhibition of skeletal muscle sodium currents by mexiletine analogues: specific hydrophobic interactions rather than lipophilia per se account for drug therapeutic profile
-
De Luca, A., Talon, S., De Bellis, M., Desaphy, J.-F., Franchini, C., Lentini, G., Catalano, A., Corbo, F., Tortorella, V., and Conte Camerino, D. (2003). Inhibition of skeletal muscle sodium currents by mexiletine analogues: specific hydrophobic interactions rather than lipophilia per se account for drug therapeutic profile. Naunyn Schmiedebergs Arch. Pharmacol. 367, 318-327.
-
(2003)
Naunyn Schmiedebergs Arch. Pharmacol
, vol.367
, pp. 318-327
-
-
De Luca, A.1
Talon, S.2
De Bellis, M.3
Desaphy, J.-F.4
Franchini, C.5
Lentini, G.6
Catalano, A.7
Corbo, F.8
Tortorella, V.9
Conte Camerino, D.10
-
12
-
-
0032737562
-
Increased hindrance on the chiral carbon atom of mexiletine enhances the block of rat skeletal muscle Na+ channels in a model of myotonia induced by ATX
-
Desaphy, J.-F., Conte Camerino, D., Franchini, C., Lentini, G., Tortorella, V., and De Luca, A. (1999). Increased hindrance on the chiral carbon atom of mexiletine enhances the block of rat skeletal muscle Na+ channels in a model of myotonia induced by ATX. Br. J. Pharmacol. 128, 1165-1174.
-
(1999)
Br. J. Pharmacol
, vol.128
, pp. 1165-1174
-
-
Desaphy, J.-F.1
Conte Camerino, D.2
Franchini, C.3
Lentini, G.4
Tortorella, V.5
De Luca, A.6
-
13
-
-
0842344628
-
Different flecainide sensitivity of hNav1.4 channels and myotonic mutants explained by state-dependent block
-
Desaphy, J.-F., De Luca, A., Didonna, M. P., George, A. L. Jr., and Conte Camerino, D. (2004). Different flecainide sensitivity of hNav1.4 channels and myotonic mutants explained by state-dependent block. J. Physiol. 554, 321-334.
-
(2004)
J. Physiol
, vol.554
, pp. 321-334
-
-
Desaphy, J.-F.1
De Luca, A.2
Didonna, M.P.3
George Jr., A.L.4
Conte Camerino, D.5
-
14
-
-
0035960574
-
Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative
-
Desaphy, J.-F., De Luca, A., Tortorella, P., De Vito, D., George, A. L. Jr., and Conte Camerino, D. (2001). Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative. Neurology 57, 1849-1857.
-
(2001)
Neurology
, vol.57
, pp. 1849-1857
-
-
Desaphy, J.-F.1
De Luca, A.2
Tortorella, P.3
De Vito, D.4
George Jr., A.L.5
Conte Camerino, D.6
-
15
-
-
77954042073
-
Molecular determinants of state-dependent block of voltage-gated sodium channels by pilsicainide
-
Desaphy, J.-F., Dipalma, A., Costanza, T., Bruno, C., Lentini, G., Franchini, C., George, A. L. Jr., and Conte Camerino, D. (2010). Molecular determinants of state-dependent block of voltage-gated sodium channels by pilsicainide. Br. J. Pharmacol. 160, 1521-1533.
-
(2010)
Br. J. Pharmacol
, vol.160
, pp. 1521-1533
-
-
Desaphy, J.-F.1
Dipalma, A.2
Costanza, T.3
Bruno, C.4
Lentini, G.5
Franchini, C.6
George Jr., A.L.7
Conte Camerino, D.8
-
16
-
-
61849100988
-
Involvement of voltage-gated sodium channels blockade in the analgesic effects of orphenadrine
-
Desaphy, J.-F., Dipalma, A., De Bellis, M., Costanza, T., Gaudioso, C., Delmas, P., George, A. L. Jr., and Conte Camerino, D. (2009). Involvement of voltage-gated sodium channels blockade in the analgesic effects of orphenadrine. Pain 142, 225-235.
-
(2009)
Pain
, vol.142
, pp. 225-235
-
-
Desaphy, J.-F.1
Dipalma, A.2
De Bellis, M.3
Costanza, T.4
Gaudioso, C.5
Delmas, P.6
George Jr., A.L.7
Conte Camerino, D.8
-
17
-
-
0037334542
-
Different ability of clenbuterol and salbutamol to block sodium channels predicts their therapeutic use in muscle excitability disorders
-
Desaphy, J.-F., Pierno, S., De Luca, A., Didonna, P., and Conte Camerino, D. (2003). Different ability of clenbuterol and salbutamol to block sodium channels predicts their therapeutic use in muscle excitability disorders. Mol. Pharmacol. 63, 659-670.
-
(2003)
Mol. Pharmacol
, vol.63
, pp. 659-670
-
-
Desaphy, J.-F.1
Pierno, S.2
De Luca, A.3
Didonna, P.4
Conte Camerino, D.5
-
18
-
-
84862555263
-
The sodium channel as a target of local anesthetic drugs
-
doi:10.3389/fphar.2011.00068
-
Fozzard, H. A., Sheets, M. F., and Hanck, D. A. (2011). The sodium channel as a target of local anesthetic drugs. Front. Pharmacol. 2:68. doi:10.3389/fphar.2011.00068
-
(2011)
Front. Pharmacol
, vol.2
, pp. 68
-
-
Fozzard, H.A.1
Sheets, M.F.2
Hanck, D.A.3
-
19
-
-
0242439310
-
Optically active mexiletine analogues as stereoselective blockers of voltage-gated Na+ channels
-
Franchini, C., Carocci, A., Catalano, A., Cavalluzzi, M. M., Corbo, F., Lentini, G., Scilimati, A., Tortorella, P., Conte Camerino, D., and De Luca, A. (2003). Optically active mexiletine analogues as stereoselective blockers of voltage-gated Na+ channels. J. Med. Chem. 46, 5238-5248.
-
(2003)
J. Med. Chem
, vol.46
, pp. 5238-5248
-
-
Franchini, C.1
Carocci, A.2
Catalano, A.3
Cavalluzzi, M.M.4
Corbo, F.5
Lentini, G.6
Scilimati, A.7
Tortorella, P.8
Conte Camerino, D.9
De Luca, A.10
-
20
-
-
70149112082
-
Using lidocaine and benzocaine to link sodium channel molecular conformations to state-dependent antiarrhythmic drug affinity
-
Hanck, D. A., Nikitina, E., McNulty, M. M., Fozzard, H. A., Lipkind, G. M., and Sheets, M. F. (2009). Using lidocaine and benzocaine to link sodium channel molecular conformations to state-dependent antiarrhythmic drug affinity. Circ. Res. 105, 492-499.
-
(2009)
Circ. Res
, vol.105
, pp. 492-499
-
-
Hanck, D.A.1
Nikitina, E.2
McNulty, M.M.3
Fozzard, H.A.4
Lipkind, G.M.5
Sheets, M.F.6
-
21
-
-
0028987938
-
Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor
-
Hidalgo, P., and MacKinnon, R. (1995). Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor. Science 268, 307-310.
-
(1995)
Science
, vol.268
, pp. 307-310
-
-
Hidalgo, P.1
MacKinnon, R.2
-
22
-
-
0017332486
-
Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction
-
Hille, B. (1977). Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction. J. Gen. Physiol. 69, 497-515.
-
(1977)
J. Gen. Physiol
, vol.69
, pp. 497-515
-
-
Hille, B.1
-
23
-
-
0032919699
-
A molecular basis for the different local anesthetic affinities of resting versus open and inactivated states of the sodium channel
-
Li, H. L., Galue, A., Meadows, L., and Ragsdale, D. S. (1999). A molecular basis for the different local anesthetic affinities of resting versus open and inactivated states of the sodium channel. Mol. Pharmacol. 55, 134-141.
-
(1999)
Mol. Pharmacol
, vol.55
, pp. 134-141
-
-
Li, H.L.1
Galue, A.2
Meadows, L.3
Ragsdale, D.S.4
-
24
-
-
27844589940
-
Molecular modelling of local anesthetic drug binding by voltagegated sodium channels
-
Lipkind, G. M., and Fozzard, H. A. (2005). Molecular modelling of local anesthetic drug binding by voltagegated sodium channels. Mol. Pharmacol. 68, 1611-1622.
-
(2005)
Mol. Pharmacol
, vol.68
, pp. 1611-1622
-
-
Lipkind, G.M.1
Fozzard, H.A.2
-
25
-
-
34249674070
-
Charge at the lidocaine binding site residues Phe-1759 affects permeation in human cardiac voltagegated sodium channels
-
McNulty, M. M., Edgerton, G. B., Shah, R. D., Hanck, D. A., Fozzard, H. A., and Lipkind, G. M. (2007). Charge at the lidocaine binding site residues Phe-1759 affects permeation in human cardiac voltagegated sodium channels. J. Physiol. 581, 741-755.
-
(2007)
J. Physiol
, vol.581
, pp. 741-755
-
-
McNulty, M.M.1
Edgerton, G.B.2
Shah, R.D.3
Hanck, D.A.4
Fozzard, H.A.5
Lipkind, G.M.6
-
26
-
-
0032794137
-
Point mutations at N434 in D1-S6 of m1 Na+ channels modulate binding affinity and stereoselectivity of local anesthetic enantiomers
-
Nau, C., Wang, S.-H., Strichartz, G. R., and Wang, G. K. (1999). Point mutations at N434 in D1-S6 of m1 Na+ channels modulate binding affinity and stereoselectivity of local anesthetic enantiomers. Mol. Pharmacol. 56, 404-413.
-
(1999)
Mol. Pharmacol
, vol.56
, pp. 404-413
-
-
Nau, C.1
Wang, S.-H.2
Strichartz, G.R.3
Wang, G.K.4
-
27
-
-
0037098723
-
Cocaine binds to a common site on open and inactivated human heart (Nav1.5) sodium channels
-
O'Leary, M. E., and Chahine, M. (2002). Cocaine binds to a common site on open and inactivated human heart (Nav1.5) sodium channels. J. Physiol. 541, 701-716.
-
(2002)
J. Physiol
, vol.541
, pp. 701-7163
-
-
O'Leary, M.E.1
Chahine, M.2
-
28
-
-
0347627648
-
Closing and inactivation potentiate the cocaethylene inhibition of cardiac sodium channels by distinct mechanisms
-
O'Leary, M. E., Digregorio, M., and Chahine, M. (2003). Closing and inactivation potentiate the cocaethylene inhibition of cardiac sodium channels by distinct mechanisms. Mol. Pharmacol. 64, 1575-1585.
-
(2003)
Mol. Pharmacol
, vol.64
, pp. 1575-1585
-
-
O'Leary, M.E.1
Digregorio, M.2
Chahine, M.3
-
29
-
-
0034128858
-
A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state
-
O'Reilly, J. P., Wang, S.-Y., and Wang, G. K. (2000). A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state. Biophys. J. 78, 773-784.
-
(2000)
Biophys. J
, vol.78
, pp. 773-784
-
-
O'Reilly, J.P.1
Wang, S.-Y.2
Wang, G.K.3
-
30
-
-
79959255073
-
Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels
-
Pless, S. A., Galpin, J. D., Frankel, A., and Ahern, C. A. (2011). Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels. Nat. Commun. 2, 351.
-
(2011)
Nat. Commun
, vol.2
, pp. 351
-
-
Pless, S.A.1
Galpin, J.D.2
Frankel, A.3
Ahern, C.A.4
-
31
-
-
0027944683
-
Molecular determinants of statedependent block of Na+ channels by local anesthetics
-
Ragsdale, D. S., McPhee, J. C., Scheuer, T., and Catterall, W. A. (1994). Molecular determinants of statedependent block of Na+ channels by local anesthetics. Science 265, 1724-1728.
-
(1994)
Science
, vol.265
, pp. 1724-1728
-
-
Ragsdale, D.S.1
McPhee, J.C.2
Scheuer, T.3
Catterall, W.A.4
-
32
-
-
0029787945
-
Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltagegated sodium channels
-
Ragsdale, D. S., McPhee, J. C., Scheuer, T., and Catterall, W. A. (1996). Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltagegated sodium channels. Proc. Natl. Acad. Sci. U.S.A. 93, 9270-9275.
-
(1996)
Proc. Natl. Acad. Sci. U.S.A
, vol.93
, pp. 9270-9275
-
-
Ragsdale, D.S.1
McPhee, J.C.2
Scheuer, T.3
Catterall, W.A.4
-
33
-
-
78549281090
-
Sodium channel molecular conformations and antiarrhythmic drug affinity
-
Sheets, M. F., Fozzard, H. A., Lipkind, G. M., and Hanck, D. A. (2010). Sodium channel molecular conformations and antiarrhythmic drug affinity. Trends Cardiovasc. Med. 20, 16-21.
-
(2010)
Trends Cardiovasc. Med
, vol.20
, pp. 16-21
-
-
Sheets, M.F.1
Fozzard, H.A.2
Lipkind, G.M.3
Hanck, D.A.4
-
34
-
-
0035056966
-
Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics
-
Sunami, A., Glaase, J. W., and Fozzard, H. A. (2001). Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics. Mol. Pharmacol. 59, 684-691.
-
(2001)
Mol. Pharmacol
, vol.59
, pp. 684-691
-
-
Sunami, A.1
Glaase, J.W.2
Fozzard, H.A.3
-
35
-
-
0033849987
-
Residues in Na+ channel D3-S6 segment modulate both batrachotoxin and local anesthetic affinities
-
Wang, S. Y., Nau, C., and Wang, G. K. (2000). Residues in Na+ channel D3-S6 segment modulate both batrachotoxin and local anesthetic affinities. Biophys. J. 79, 1379-1387.
-
(2000)
Biophys. J
, vol.79
, pp. 1379-1387
-
-
Wang, S.Y.1
Nau, C.2
Wang, G.K.3
-
36
-
-
0031725974
-
Lysine point mutations in Na+ channel D4-S6 reduce inactivated channel block by local anesthetics
-
Wright, S. N., Wang, S. Y., and Wang, G. K. (1998). Lysine point mutations in Na+ channel D4-S6 reduce inactivated channel block by local anesthetics. Mol. Pharmacol. 54, 733-739.
-
(1998)
Mol. Pharmacol
, vol.54
, pp. 733-739
-
-
Wright, S.N.1
Wang, S.Y.2
Wang, G.K.3
-
37
-
-
0034813630
-
Point mutations in α-subunit of human cardiac Na+ channels alter Na+ current kinetics
-
Xiao, Y.-F., Ke, Q., Wang, S.-Y., Yang, Y., Wang, G. K., Morgan, J. P., and Leaf, A. (2001). Point mutations in α-subunit of human cardiac Na+ channels alter Na+ current kinetics. Biochem. Biophys. Res. Commun. 281, 45-52.
-
(2001)
Biochem. Biophys. Res. Commun
, vol.281
, pp. 45-52
-
-
Xiao, Y.-F.1
Ke, Q.2
Wang, S.-Y.3
Yang, Y.4
Wang, G.K.5
Morgan, J.P.6
Leaf, A.7
-
38
-
-
0035808309
-
Molecular determinants of voltagedependent gating and binding of pore-blocking drugs in transmembrane segment IIIS6 of the Na+ channelasubunit
-
Yarov-Yarovoy, V., Brown, J., Sharp, E. M., Clare, J. J., Scheuer, T., and Catterall, W. A. (2001). Molecular determinants of voltagedependent gating and binding of pore-blocking drugs in transmembrane segment IIIS6 of the Na+ channelasubunit.J.Biol.Chem.276, 20-27.
-
(2001)
J. Biol.hem.
, vol.276
, pp. 20-27
-
-
Yarov-Yarovoy, V.1
Brown, J.2
Sharp, E.M.3
Clare, J.J.4
Scheuer, T.5
Catterall, W.A.6
-
39
-
-
0037144493
-
Role of amino acid residues in transmembrane segments IS6 and IIS6 of the Na+ channel a subunit in voltage-dependent gating and drug block
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Yarov-Yarovoy, V., McPhee, J. C., Idsvoog, D., Pate, C., Scheuer, T., and Catterall, W. A. (2002). Role of amino acid residues in transmembrane segments IS6 and IIS6 of the Na+ channel a subunit in voltage-dependent gating and drug block. J. Biol. Chem. 277, 35393-35401.
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(2002)
J. Biol. Chem
, vol.277
, pp. 35393-35401
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Yarov-Yarovoy, V.1
McPhee, J.C.2
Idsvoog, D.3
Pate, C.4
Scheuer, T.5
Catterall, W.A.6
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