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Volumn 3, Issue 2, 2011, Pages 223-241

Conformationally restricted GABA analogs: From rigid carbocycles to cage hydrocarbons

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOMETHYLCYCLOPROPANE 1 CARBOXYLIC ACID; 3 AMINOCYCLOBUTANE CARBOXYLIC ACID; 3 AMINOCYCLOPENTANECARBOXYLIC ACID; 4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID DERIVATIVE; ADAMANTANE; BICYLCO[3.3.1]NONANE; CYCLOBUTANE; CYCLOHEXANE; CYCLOPROPANE; GABAPENTIN; HYDROCARBON; NORBORNANE; UNCLASSIFIED DRUG;

EID: 79951588185     PISSN: 17568919     EISSN: None     Source Type: Journal    
DOI: 10.4155/fmc.10.287     Document Type: Review
Times cited : (20)

References (74)
  • 1
    • 0002587841 scopus 로고
    • γ-aminobutyric acid in brain: Its formation from glutamic acid
    • Roberts E, Frankel S. γ-aminobutyric acid in brain: its formation from glutamic acid. J. Biol. Chem. 187, 55-63 (1950).
    • (1950) J. Biol. Chem. , vol.187 , pp. 55-63
    • Roberts, E.1    Frankel, S.2
  • 2
    • 70449251556 scopus 로고
    • Membrane permeability change during inhibitory transmitter action in crustacean muscle
    • Boistel J, Fatt P. Membrane permeability change during inhibitory transmitter action in crustacean muscle. J. Physiol. (Lond.) 144, 176-191 (1958).
    • (1958) J. Physiol. (Lond.) , vol.144 , pp. 176-191
    • Boistel, J.1    Fatt, P.2
  • 3
    • 77049235740 scopus 로고
    • The specific ionic conductances and the ionic movements across the motoneuronal membrane that produce the inhibitory postsynaptic potential
    • Coombs JS, Eccles JC, Fatt P. The specific ionic conductances and the ionic movements across the motoneuronal membrane that produce the inhibitory postsynaptic potential. J. Physiol. (Lond.) 130, 326-373 (1955).
    • (1955) J. Physiol. (Lond.) , vol.130 , pp. 326-373
    • Coombs, J.S.1    Eccles, J.C.2    Fatt, P.3
  • 4
    • 0014040410 scopus 로고
    • The action of γ-aminobutyric acid on cortical neurones
    • Krnjevic K, Schwartz S. The action of γ-aminobutyric acid on cortical neurones. Exp. Brain Res. 3, 320-336 (1967).
    • (1967) Exp. Brain Res. , vol.3 , pp. 320-336
    • Krnjevic, K.1    Schwartz, S.2
  • 5
    • 0018349345 scopus 로고
    • 3H]GABA binding to postsynaptic receptors in human cerebellum
    • Nicholson SH, Suckling CJ, Iversen LL. GABA analogues: conformational analysis of effects on [3H]GABA binding to postsynaptic receptors in human cerebellum. J. Neurochem. 32, 249-252 (1979). (Pubitemid 9108959)
    • (1979) Journal of Neurochemistry , vol.32 , Issue.1 , pp. 249-252
    • Nicholson, S.H.1    Suckling, C.J.2    Iversen, L.L.3
  • 7
    • 0016770442 scopus 로고
    • Characterisation of an inhibitory receptor in rat hippocampus: A microiontophoretic study using conformationally restricted amino acid analogues
    • Segal M, Sims K, Andsmissman E. Characterisation of an inhibitory receptor in rat hippocampus: a microiontophoretic study using conformationally restricted amino acid analogues. Br. J. Pharmacol. 54, 181-188 (1975).
    • (1975) Br. J. Pharmacol. , vol.54 , pp. 181-188
    • Segal, M.1    Sims, K.2    Andsmissman, E.3
  • 8
    • 0000976591 scopus 로고
    • A systematic study of GABA analogues of restricted conformation
    • Kofod H, Krogsgaard-Larsen P, Scheel-Kruger J (Eds). Munksgaard, Copenhagen, Denmark
    • Johnston GAR, Allan RD, Kennedy SME, Twitchin B. A systematic study of GABA analogues of restricted conformation. In:GABA-Neurotransmitters . Kofod H, Krogsgaard-Larsen P, Scheel-Kruger J (Eds). Munksgaard, Copenhagen, Denmark 149-164 (1978).
    • (1978) GABA-Neurotransmitters , pp. 149-164
    • Johnston, G.A.R.1    Allan, R.D.2    Sme, K.3    Twitchin, B.4
  • 10
    • 0016828208 scopus 로고
    • Structure and biological activity of a series of conformationalty restricted analogues of GABA
    • Krogsgaard-Larsen P, Johnston GAR, Curtis DR, Game CJA, Mcculloch RM. Structure and biological activity of a series of conformationalty restricted analogues of GABA. J. Neurochem. 25, 803-809 (1975).
    • (1975) J. Neurochem. , vol.25 , pp. 803-809
    • Krogsgaard-Larsen, P.1    Johnston, G.A.R.2    Curtis, D.R.3    Cja, G.4    McCulloch, R.M.5
  • 11
    • 0018840893 scopus 로고
    • The synthesis and activity of cis- and trans-2-(aminomethyl) cyclopropanecarboxylic acid as conformationally restricted analogues of GABA
    • DOI 10.1111/j.1471-4159.1980.tb11193.x
    • Allan RD, Curtis DR, Headley P, Johnson DR, Lodge D, Twitchin B. The synthesis and activity of cis-and trans-2- (aminomethyl) cyclopropanecarboxylic acid as conformationally restricted analogues of GABA. J. Neurochem. 34(3), 652-654 (1980). (Pubitemid 10165083)
    • (1980) Journal of Neurochemistry , vol.34 , Issue.3 , pp. 652-654
    • Allan, R.D.1    Curtis, D.R.2    Headley, P.M.3
  • 12
    • 84986706383 scopus 로고
    • Ein effektiver Weg zu GABA-analogen Aminosauren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen
    • Paulini K, Reissig H-U. Ein effektiver Weg zu GABA-analogen Aminosauren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen. Liebigs Ann. Chem. 455-461 (1991).
    • (1991) Liebigs Ann. Chem. , pp. 455-461
    • Paulini, K.1    Reissig, H.-U.2
  • 13
    • 0031023870 scopus 로고    scopus 로고
    • From 3-aza-2-oxobicyclo[3.1.0]hexane to enantiopure disubstituted cyclopropane: A convenient approach to cis-2,3-methano-GABA
    • DOI 10.1016/S0957-4166(96)00477-6, PII S0957416696004776
    • Galeazzi R, Mobbili G, Orena M. From 3-aza-2-oxobicyclo[3.1.0]hexane to enantiopure disubstituted cyclopropane: a convenient approach to cis-2,3-methano- GABA. Tetrahedron. Asymm. 8(1), 133-137 (1997). (Pubitemid 27039333)
    • (1997) Tetrahedron Asymmetry , vol.8 , Issue.1 , pp. 133-137
    • Galeazzi, R.1    Mobbili, G.2    Orena, M.3
  • 14
    • 0030059325 scopus 로고    scopus 로고
    • A convenient approach to diastereomerically pure 1,3,4-trisubstituted pyrrolidin-2-ones by intramolecular cyclisation of N-(2-alken-1-yl) amides mediated by Mn(III). An entry to both (R)- and (S)-3-pyrrolidineacetic acid
    • Galeazzi R, Mobbili G, Orena M. A convenient approach to diastereomerically pure 1,3,4-trisubstituted pyrrolidin-2-ones by intramolecular cyclisation of N-(2-alken-1-yl) amides mediated by Mn(III). An entry to both (R)- and (S)-3-pyrrolidineacetic acid. Tetrahedron 52, 1069-1084 (1996).
    • (1996) Tetrahedron , vol.52 , pp. 1069-1084
    • Galeazzi, R.1    Mobbili, G.2    Orena, M.3
  • 15
    • 39149129355 scopus 로고    scopus 로고
    • A novel stereoselective tin-free radical protocol for the enantioselective synthesis of pyrrolidinones and its application to the synthesis of biologically active GABA-derivatives
    • Rodríguez-Soria V, Quintero L, Sartillo-Piscil F. A novel stereoselective tin-free radical protocol for the enantioselective synthesis of pyrrolidinones and its application to the synthesis of biologically active GABA-derivatives. Tetrahedron 64, 2750-2754 (2008).
    • (2008) Tetrahedron , vol.64 , pp. 2750-2754
    • Rodríguez-Soria, V.1    Quintero, L.2    Sartillo-Piscil, F.3
  • 16
    • 0032540969 scopus 로고    scopus 로고
    • Resolution and conformational analysis of diastereoisomeric esters of cis- and trans-2-(aminomethyl)-1-carboxycyclopropanes
    • DOI 10.1016/S0957-4166(98)00250-X, PII S095741669800250X
    • Duke RK, Allan RD, Chebib M, Greenwood JR, Johnson DR. Resolution and conformational analysis of diastereoisomeric esters of cis- and trans-2-(aminomethyl)-1- carboxycyclopropanes. Tetrahedron Assym. 9, 2533-2548 (1998). (Pubitemid 28374948)
    • (1998) Tetrahedron Asymmetry , vol.9 , Issue.14 , pp. 2533-2548
    • Duke, R.K.1    Allan, R.D.2    Chebib, M.3    Greenwood, J.R.4    Johnston, G.A.R.5
  • 17
    • 0033769321 scopus 로고    scopus 로고
    • (+)- and (-)-cis-2-aminomethylcyclopropanecarboxylic acids show opposite pharmacology at recombinant r1 and r2 GABAC receptors
    • Duke RK, Chebib M, Balcar VJ, Allan RD, Mewett KN, Johnson GAR. (+)- and (-)-cis-2-aminomethylcyclopropanecarboxylic acids show opposite pharmacology at recombinant r1 and r2 GABAC receptors. J. Neurochem. 75(6), 2602-2610 (2000).
    • (2000) J. Neurochem. , vol.75 , Issue.6 , pp. 2602-2610
    • Duke, R.K.1    Chebib, M.2    Balcar, V.J.3    Allan, R.D.4    Mewett, K.N.5    Johnson, G.A.R.6
  • 19
    • 0036400032 scopus 로고    scopus 로고
    • Application of polymer-supported enzymes and reagents in the synthesis of γ-aminobutyric acid (GABA) analogues
    • Baxendale IR, Ernst M, Krahnert W-R, Ley SV. Application of polymer-supported enzymes and reagents in the synthesis of γ-aminobutyric acid (GABA) analogues. Synlett 10, 1641-1644 (2002). (Pubitemid 35190739)
    • (2002) Synlett , Issue.10 , pp. 1641-1644
    • Baxendale, I.R.1    Ernst, M.2    Krahnert, W.-R.3    Ley, S.V.4
  • 20
    • 0026542486 scopus 로고
    • Enantioselective synthesis of (+) and (-)-cis-3-aminocyclo- pentanecarboxylic acids by enzymatic asymmetrization
    • Chenevert R, Martin R. Enantioselective synthesis of (+) and (-)-cis-3-aminocyclo-pentanecarboxylic acids by enzymatic asymmetrization. Tetrahedron Asymm. 3, 199-200 (1992).
    • (1992) Tetrahedron Asymm. , vol.3 , pp. 199-200
    • Chenevert, R.1    Martin, R.2
  • 21
    • 0018618772 scopus 로고
    • Synthesis of analogues of GABA. II. All four stereoisomers of 3-aminocyclopentanecarboxylic acid and a stereochemical correlation with amidinomycin
    • Allan RD, Johnson DR, Twitchin B. Synthesis of analogues of GABA. III. All four stereo-isomers of 3-aminocyclo-pentanecarboxylicacid and a stereochemical correlation with amidinomycin. Aust. J. Chem. 32, 2517-2521 (1979). (Pubitemid 10077753)
    • (1979) Australian Journal of Chemistry , vol.32 , Issue.11 , pp. 2517-2521
    • Allan, R.D.1    Johnston, G.A.R.2    Twitchin, B.3
  • 23
    • 2942748279 scopus 로고    scopus 로고
    • Anticonvulsants and the relief of chronic pain: Pregabalin and gabapentin as a2d ligands at voltage-gated calcium channels
    • Stahl S. Anticonvulsants and the relief of chronic pain: pregabalin and gabapentin as a2d ligands at voltage-gated calcium channels. J. Clin. Psychiatry 65, 596-597 (2004).
    • (2004) J. Clin. Psychiatry , vol.65 , pp. 596-597
    • Stahl, S.1
  • 25
    • 0032819783 scopus 로고    scopus 로고
    • Gabapentin in the management of convulsive disorders
    • DOI 10.1111/j.1528-1157.1999.tb00932.x
    • McLean M. Gabapentin in the management of convulsive disorders. Epilepsia 40 (Suppl. 6), S39-S50 (1999). (Pubitemid 29481921)
    • (1999) Epilepsia , vol.40 , Issue.SUPPL. 6
    • McLean, M.J.1
  • 27
    • 0034750718 scopus 로고    scopus 로고
    • Gabapentin in postherpetic neuralgia: A randomised, double blind, placebo controlled study
    • DOI 10.1016/S0304-3959(01)00407-9, PII S0304395901004079
    • Rice A, Maton S. Gabapentin in postherpetic neuralgia: a randomised, double blind, placebo controlled study. Pain 94, 215-224 (2001). (Pubitemid 33016615)
    • (2001) Pain , vol.94 , Issue.2 , pp. 215-224
    • Rice, A.S.C.1    Maton, S.2
  • 28
    • 0037180403 scopus 로고    scopus 로고
    • Treatment of restless legs syndrome with gabapentin: A double-blind, cross-over study
    • Garcia-Borreguero D, Larrosa O, de la Llave Y, Verger K, Masramon X, Hernandez G. Treatment of restless legs syndrome with gabapentin: a double-blind, cross-over study. Neurology 59, 1573-1579 (2002). (Pubitemid 35387065)
    • (2002) Neurology , vol.59 , Issue.10 , pp. 1573-1579
    • Garcia-Borreguero, D.1    Larrosa, O.2    De La Llave, Y.3    Verger, K.4    Masramon, X.5    Hernandez, G.6
  • 29
    • 0031802463 scopus 로고    scopus 로고
    • Gabapentin as a potential treatment for anxiety disorders [1]
    • Pollack M, Matthews J, Scott E. Gabapentin as a potential treatment for anxiety disorders. Am. J. Psychiatry 155, 992-993 (1998). (Pubitemid 28307619)
    • (1998) American Journal of Psychiatry , vol.155 , Issue.7 , pp. 992-993
    • Pollack, M.H.1    Matthews, J.2    Scott, E.L.3
  • 31
    • 0029057902 scopus 로고
    • Gabapentin
    • McLean M. Gabapentin. Epilepsia 36 (Suppl. 2), S73-S86 (1995).
    • (1995) Epilepsia , vol.36 , Issue.SUPPL. 2
    • McLean, M.1
  • 32
    • 0034129145 scopus 로고    scopus 로고
    • Inter- and intra-subject variability in gabapentin absorption and absolute bioavailability
    • DOI 10.1016/S0920-1211(00)00117-0, PII S0920121100001170
    • Gidal B, Radulovic L, Kruger S, Rutecki P, Pitterle M, Bockbrader H. Inter- and intra-subject variability in gabapentin absorption and absolute bioavailability. Epilepsy Res. 40, 123-127 (2000). (Pubitemid 30339403)
    • (2000) Epilepsy Research , vol.40 , Issue.2-3 , pp. 123-127
    • Gidal, B.E.1    Radulovic, L.L.2    Kruger, S.3    Rutecki, P.4    Pitterle, M.5    Bockbrader, H.N.6
  • 33
    • 0032958091 scopus 로고    scopus 로고
    • Effects of age and gender on single-dose pharmacokinetics of gabapentin
    • Boyd R, Turck D, Abel R, Sedman A, Bockbrader H. Effects of age and gender on single-dose pharmacokinetics of gabapentin. Epilepsia 40, 474-479 (1999). (Pubitemid 29164860)
    • (1999) Epilepsia , vol.40 , Issue.4 , pp. 474-479
    • Boyd, R.A.1    Trck, D.2    Abel, R.B.3    Sedman, A.J.4    Bockbrader, H.N.5
  • 35
    • 0033018825 scopus 로고    scopus 로고
    • 3-substituted GABA analogs with central nervous system activity: A review
    • DOI 10.1002/(SICI)1098-1128(199903)19:2<149::AID-MED3>3.0.CO;2-B
    • Bryans JS, Wustrow DJ. 3-substituted GABA analogs with central nervous system activity: a review. Med. Res. Rev. 19(2), 149-177 (1999). (Pubitemid 29124983)
    • (1999) Medicinal Research Reviews , vol.19 , Issue.2 , pp. 149-177
    • Bryans, J.S.1    Wustrow, D.J.2
  • 36
    • 0026033643 scopus 로고
    • Novel syntheses of gabapentin via addition of hydrocyanic acid to cyclohexylidenemalonate or cyano(cyclohexylidene)acetate
    • Griffiths G, Mettler H, Mills L, Previdoli F. Novel syntheses of gabapentin via addition of hydrocyanic acid to cyclohexylidenemalonate or cyano(cyclohexylidene)acetate. Helv. Chim. Acta 74, 309-314 (1991).
    • (1991) Helv. Chim. Acta , vol.74 , pp. 309-314
    • Griffiths, G.1    Mettler, H.2    Mills, L.3    Previdoli, F.4
  • 39
    • 0141954291 scopus 로고    scopus 로고
    • The neuropharmacological basis for the use of memantine in the treatment of Alzheimer's disease
    • Rogawski MA, Wenk GL. The neuropharmacological basis for the use of memantine in the treatment of Alzheimer's disease. CNS Drug Rev. 9(3), 275-308 (2003). (Pubitemid 37254706)
    • (2003) CNS Drug Reviews , vol.9 , Issue.3 , pp. 275-308
    • Rogawski, M.A.1    Wenk, G.L.2
  • 40
    • 34250275190 scopus 로고
    • Action of midantane, remantadine, and its alkyl analogs on the central nervous system
    • Germane SK, Polis YY, Karinya LY. Action of midantane, remantadine, and its alkyl analogs on the central nervous system. Pharmaceut. Chem. J. 11(6), 798-802 (1977).
    • (1977) Pharmaceut. Chem. J. , vol.11 , Issue.6 , pp. 798-802
    • Germane, S.K.1    Polis, Y.Y.2    Karinya, L.Y.3
  • 41
    • 79951597353 scopus 로고
    • Influence of adapromin on the content of catecholamines in the body of white rats
    • Berzinya DA, Kimenis AA. Influence of adapromin on the content of catecholamines in the body of white rats. Exp. Clin. Farmacoterapia 15, 50-53 (1986).
    • (1986) Exp. Clin. Farmacoterapia , vol.15 , pp. 50-53
    • Berzinya, D.A.1    Kimenis, A.A.2
  • 42
    • 27144512985 scopus 로고    scopus 로고
    • Comparative analysis of the effects of adapromine, midantane, and bromantane on bioelectrical activity of rat brain
    • Krapivin SV, Sergeeva SA. Comparative analysis of the effects of adapromine, midantane, and bromantane on bioelectrical activity of rat brain. Bull. Exp. Biol. Med. 125(2), 151-155 (1998). (Pubitemid 128695359)
    • (1998) Bulletin of Experimental Biology and Medicine , vol.125 , Issue.2 , pp. 151-155
    • Krapivin, S.V.1    Sergeeva, S.A.2    Morozov, I.S.3
  • 44
    • 0019042753 scopus 로고
    • Pharmacokinetic study of 2-(N-benzylamino) adamatane (bemantan) by a gas-liquid chromatographic method
    • Liubimov BI, Skoldinov AP, Boiko SS. Pharmacokinetic study of 2-(N-benzylamino) adamatane (bemantan) by a gas-liquid chromatographic method. Farmakol. Toksikol. 43(4), 408-411 (1980).
    • (1980) Farmakol. Toksikol. , vol.43 , Issue.4 , pp. 408-411
    • Liubimov, B.I.1    Skoldinov, A.P.2    Boiko, S.S.3
  • 45
    • 79951640729 scopus 로고
    • Interspecific differences in kemantan pharmacokinetics
    • Boiko SS, Zherdev VP, Kisliak NA. Interspecific differences in kemantan pharmacokinetics. Farmakol. Toksikol. 1991(54), 1 (1991).
    • (1991) Farmakol. Toksikol. , vol.1991 , Issue.54 , pp. 1
    • Boiko, S.S.1    Zherdev, V.P.2    Kisliak, N.A.3
  • 48
    • 79951609682 scopus 로고    scopus 로고
    • Unusual solid state properties of cubane discovered
    • Taylor BN. Unusual solid state properties of cubane discovered. J. Res. NIST 102(5), 600 (1997).
    • (1997) J. Res. NIST , vol.102 , Issue.5 , pp. 600
    • Taylor, B.N.1
  • 50
    • 0040648436 scopus 로고
    • Chemistry and structure of phenylcubanes
    • Bashir-Hashemi A. Chemistry and structure of phenylcubanes. J. Org. Chem. 55(2), 416-420 (1990).
    • (1990) J. Org. Chem. , vol.55 , Issue.2 , pp. 416-420
    • Bashir-Hashemi, A.1
  • 52
    • 10344221023 scopus 로고    scopus 로고
    • Pharmacology and structure-activity relationships of bioactive polycyclic cage compounds: A focus on pentacycloundecane derivatives
    • DOI 10.1002/med.20013
    • Geldenhuys WJ, Malan SF, Marchand AP. Pharmacology and structure-activity relationships of bioactive polycyclic cage compounds: a focus on pentacycloundecane derivatives. Med. Res. Rev. 25(1), 21-48 (2005). (Pubitemid 39628525)
    • (2005) Medicinal Research Reviews , vol.25 , Issue.1 , pp. 21-48
    • Geldenhuys, W.J.1    Malan, S.F.2    Bloomquist, J.R.3    Marchand, A.P.4    Van Der Schyf, C.J.5
  • 54
    • 4744346398 scopus 로고
    • Preparation of 4-substituted-bicyclo[2.2.1]heptane-1- carboxylic acids
    • Wilcox C Jr, Leung C. Preparation of 4-substituted-bicyclo[2.2.1]heptane- 1- carboxylic acids. J. Org. Chem. 33(2), 877-880 (1968).
    • (1968) J. Org. Chem. , vol.33 , Issue.2 , pp. 877-880
    • Wilcox Jr., C.1    Leung, C.2
  • 55
    • 0001055177 scopus 로고
    • Antiviral activity of 1-adamantanamine (amantadine)
    • Davies WL, Grunert RR, Haff RF et al. Antiviral activity of 1-adamantanamine (amantadine). Science 144, 862-863 (1964).
    • (1964) Science , vol.144 , pp. 862-863
    • Davies, W.L.1    Grunert, R.R.2    Haff, R.F.3
  • 56
    • 0035562296 scopus 로고    scopus 로고
    • Amantadine: Anantiviral and antiparkinsonian agent
    • Stanicova J, Miskovsky P, Sutiak V. Amantadine: anantiviral and antiparkinsonian agent. Vet. Med. Czech 46, 224-256 (2001).
    • (2001) Vet. Med. Czech , vol.46 , pp. 224-256
    • Stanicova, J.1    Miskovsky, P.2    Sutiak, V.3
  • 57
    • 0032898676 scopus 로고    scopus 로고
    • The roles of amantadine, rimantadine, ursodeoxycholic acid, and NSAIDs, alone or in combination with alpha interferons, in the treatment of chronic hepatitis C
    • Younossi ZM, Perrillo RP. The roles of amantadine, rimantadine, ursodeoxycholic acid, and NSAIDs, alone or in combination with alpha interferons, in the treatment of chronic hepatitis C. Semin. Liver Dis. 19(Suppl. 1), 662-668 (1999).
    • (1999) Semin. Liver Dis. , vol.19 , Issue.SUPPL. 1 , pp. 662-668
    • Younossi, Z.M.1    Perrillo, R.P.2
  • 59
    • 0020637423 scopus 로고
    • Prevention of post-herpetic neuralgia by amantadine hydrochloride (Symmetrel)
    • Galbraith AW. Prevention of post-herpetic neuralgia by amantadine hydrochloride (Symmetrel). Br. J. Clin. Pract. 37, 304-306 (1983). (Pubitemid 13050288)
    • (1983) British Journal of Clinical Practice , vol.37 , Issue.9 , pp. 304-306
    • Galbraith, A.W.1
  • 60
    • 0021928605 scopus 로고
    • Nontraditional analgesics for the management of postherpetic neuralgia
    • Thompson M, Bones M. Nontraditional analgesics for the management of postherpetic neuralgia. Clin. Pharm. 4, 170-176 (1985). (Pubitemid 15143687)
    • (1985) Clinical Pharmacy , vol.4 , Issue.2 , pp. 170-176
    • Thompson, M.1    Bones, M.2
  • 61
    • 57749105458 scopus 로고    scopus 로고
    • Polycyclic compounds: Ideal drug scaffolds for the design of multiple mechanism drugs?
    • Van der Schyf CJ, Geldenhuys WJ. Polycyclic compounds: ideal drug scaffolds for the design of multiple mechanism drugs? Neurotherapeutics 6(1), 175 (2009).
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 175
    • Van Der Schyf, C.J.1    Geldenhuys, W.J.2
  • 62
    • 37049100600 scopus 로고
    • Synthesis of the four stereoisomers of 4-aminoadamantane-2-carboxylic acid, rigid analogues of γ-aminobutyric acid
    • Black RM. Synthesis of the four stereoisomers of 4-aminoadamantane-2- carboxylic acid, rigid analogues of γ-aminobutyric acid. J. Chem. Soc. Perkin Trans. 1, 73-77 (1982).
    • (1982) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 73-77
    • Black, R.M.1
  • 64
    • 34250652923 scopus 로고    scopus 로고
    • Schreiner PR. g-aminoadamantanecarboxylic acids through direct C-H bond amidations
    • Wanka L, Cabrele C, Vanejews M, Schreiner PR. g-aminoadamantanecarboxylic acids through direct C-H bond amidations. Eur. J. Org. Chem. 2007(9), 1474-1490 (2007).
    • (2007) Eur. J. Org. Chem. , vol.2007 , Issue.9 , pp. 1474-1490
    • Wanka, L.1    Cabrele, C.2    Vanejews, M.3
  • 65
    • 84989490599 scopus 로고
    • Synthetic methods and reactions; 661. nitrosonium ion induced preparation of amides from alkyl (arylalkyl) halides with nitriles, a mild and selective ritter-type reaction
    • Olah GA, Gupta GB, Narang SC. Synthetic methods and reactions; 661. nitrosonium ion induced preparation of amides from alkyl (arylalkyl) halides with nitriles, a mild and selective ritter-type reaction. Synthesis 274-276 (1979).
    • (1979) Synthesis , pp. 274-276
    • Olah, G.A.1    Gupta, G.B.2    Narang, S.C.3
  • 72
    • 79951661513 scopus 로고    scopus 로고
    • Jennings R, Johnson D, Seamans R, Zeller J. US5319135 (1994)
    • Jennings R, Johnson D, Seamans R, Zeller J. US5319135 (1994).
  • 73
    • 79951590661 scopus 로고    scopus 로고
    • Ferrari M, Ghezzi M, Belotti P. US6846950 (2005)
    • Ferrari M, Ghezzi M, Belotti P. US6846950 (2005).
  • 74
    • 79951607363 scopus 로고    scopus 로고
    • Geigy JR. NL6600715 (1966)
    • Geigy JR. NL6600715 (1966).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.