메뉴 건너뛰기




Volumn 6, Issue 10, 2014, Pages 1179-1199

Selective sigma-1 receptor antagonists for the treatment of pain

Author keywords

[No Author keywords available]

Indexed keywords

OPIATE ANTAGONIST; SIGMA 1 OPIATE RECEPTOR; SIGMA 1 RECEPTOR ANTAGONIST; SIGMA OPIATE RECEPTOR; UNCLASSIFIED DRUG; ANALGESIC AGENT; SIGMA-1 RECEPTOR;

EID: 84905510106     PISSN: 17568919     EISSN: 17568927     Source Type: Journal    
DOI: 10.4155/fmc.14.54     Document Type: Review
Times cited : (47)

References (118)
  • 1
    • 79959761736 scopus 로고    scopus 로고
    • Treatment of chronic non-cancer pain
    • Turk DC, Wilson HD, Cahana A. Treatment of chronic non-cancer pain. Lancet 377, 2226-2235 (2011
    • (2011) Lancet , vol.377 , pp. 2226-2235
    • Turk, D.C.1    Wilson, H.D.2    Cahana, A.3
  • 2
    • 80053510653 scopus 로고    scopus 로고
    • Pain as a global public health priority
    • Goldberg DS, McGee SJ. Pain as a global public health priority. BMC Public Health 11, 770 (2011
    • (2011) BMC Public Health , vol.11 , Issue.770
    • Goldberg, D.S.1    McGee, S.J.2
  • 3
    • 79551601675 scopus 로고    scopus 로고
    • Combination drug therapy for chronic pain: A call for more clinical studies
    • Mao J, Gold MS, Backonja M. Combination drug therapy for chronic pain: A call for more clinical studies. J. Pain 12, 157-166 (2011
    • (2011) J. Pain , vol.12 , pp. 157-166
    • Mao, J.1    Gold, M.S.2    Backonja, M.3
  • 5
    • 0017064976 scopus 로고
    • The effects of morphine-And nalorphine-like drugs in the nondependent and morphine-dependent chronic spinal dog
    • Martin WR, Eades CG, Thompson JA et al. The effects of morphine-And nalorphine-like drugs in the nondependent and morphine-dependent chronic spinal dog. J. Pharmacol. Exp. Ther. 197, 517-532 (1976
    • (1976) J. Pharmacol. Exp. Ther , vol.197 , pp. 517-532
    • Martin, W.R.1    Eades, C.G.2    Thompson, J.A.3
  • 6
    • 78650664286 scopus 로고    scopus 로고
    • Early development of sigma-receptor ligands
    • Narayanan S, Bhat R, Mesangeau C et al. Early development of sigma-receptor ligands. Future Med. Chem. 3, 79-94 (2011
    • (2011) Future Med. Chem , vol.3 , pp. 79-94
    • Narayanan, S.1    Bhat, R.2    Mesangeau, C.3
  • 7
    • 0028180570 scopus 로고
    • Rat liver and kidney contain high densities of sigma 1 and sigma 2 receptors: Characterization by ligand binding and photoaffinity labeling
    • Hellewell SB, Bruce A, Feinstein G et al. Rat liver and kidney contain high densities of sigma 1 and sigma 2 receptors: Characterization by ligand binding and photoaffinity labeling. Eur. J. Pharmacol. 268, 9-18 (1994
    • (1994) Eur. J. Pharmacol , vol.268 , pp. 9-18
    • Hellewell, S.B.1    Bruce, A.2    Feinstein, G.3
  • 8
    • 84867375290 scopus 로고    scopus 로고
    • Sigma 1 receptor chaperone: Pharmacology and therapeutic perspective
    • Botana LM, Loza M (Eds John Wiley & Sons, NJ, USA
    • Zamanillo D, Portillo-Salido E, Vela JM, Romero L. Sigma 1 receptor chaperone: Pharmacology and therapeutic perspective. In: Therapeutic Targets. Botana LM, Loza M (Eds). John Wiley & Sons, NJ, USA, 225-278 (2012
    • (2012) Therapeutic Targets , pp. 225-278
    • Zamanillo, D.1    Portillo-Salido, E.2    Vela, J.M.3    Romero, L.4
  • 9
    • 13244284747 scopus 로고    scopus 로고
    • Phenytoin differentially modulates the affinity of agonist and antagonist ligands for sigma 1 receptors of guinea pig brain
    • Cobos EJ, Baeyens JM, Del Pozo E. Phenytoin differentially modulates the affinity of agonist and antagonist ligands for sigma 1 receptors of guinea pig brain. Synapse 55, 192-195 (2005
    • (2005) Synapse , vol.55 , pp. 192-195
    • Cobos, E.J.1    Baeyens, J.M.2    Del Pozo, E.3
  • 11
    • 84875214585 scopus 로고    scopus 로고
    • Investigation of s receptors agonist/antagonist activity through N-(6-methoxytetralin-1-yl)-And N-(6-methoxynaphthalen-1-yl) alkyl derivatives of polymethylpiperidines
    • Niso M, Abate C, Ferorelli S et al. Investigation of s receptors agonist/antagonist activity through N-(6-methoxytetralin-1-yl)-And N-(6-methoxynaphthalen-1-yl) alkyl derivatives of polymethylpiperidines. Bioorg. Med. Chem. 7, 1865-1869 (2013
    • (2013) Bioorg. Med. Chem , vol.7 , pp. 1865-1869
    • Niso, M.1    Abate, C.2    Ferorelli, S.3
  • 12
    • 84884480040 scopus 로고    scopus 로고
    • The s2 receptor: A novel protein for the imaging and treatment of cancer
    • Mach RH, Zeng C, Hawkins WG. The s2 receptor: A novel protein for the imaging and treatment of cancer. J. Med. Chem. 56, 7137-7160 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 7137-7160
    • MacH, R.H.1    Zeng, C.2    Hawkins, W.G.3
  • 13
    • 84857130955 scopus 로고    scopus 로고
    • The therapeutic potential of sigma (s) receptors for the treatment of central nervous system diseases: Evaluation of the evidence
    • Banister S, Kassiou M. The therapeutic potential of sigma (s) receptors for the treatment of central nervous system diseases: Evaluation of the evidence. Curr. Pharm. Design 18, 884-901 (2012
    • (2012) Curr. Pharm. Design , vol.18 , pp. 884-901
    • Banister, S.1    Kassiou, M.2
  • 14
    • 0029797712 scopus 로고    scopus 로고
    • Purification, molecular cloning, and expression of the mammalian sigma-1 binding site
    • Hanner M, Moebius FF, Flandorfer A et al. Purification, molecular cloning, and expression of the mammalian sigma-1 binding site. Proc. Natl Acad. Sci. USA 93, 8072-8077 (1996
    • (1996) Proc. Natl Acad. Sci. USA , vol.93 , pp. 8072-8077
    • Hanner, M.1    Moebius, F.F.2    Flandorfer, A.3
  • 15
    • 79960099287 scopus 로고    scopus 로고
    • Identification of the PGRMC1 protein complex as the putative sigma-2 receptor binding site
    • Xu J, Zeng C, Chu W et al. Identification of the PGRMC1 protein complex as the putative sigma-2 receptor binding site. Nat. Commun. 2, 380 (2011
    • (2011) Nat. Commun , vol.2 , Issue.380
    • Xu, J.1    Zeng, C.2    Chu, W.3
  • 16
    • 70349116879 scopus 로고    scopus 로고
    • The pharmacology of sigma-1 receptors
    • Maurice T, Su TP. The pharmacology of sigma-1 receptors. Pharmacol. Ther. 124, 195-206 (2009
    • (2009) Pharmacol. Ther , vol.124 , pp. 195-206
    • Maurice, T.1    Su, T.P.2
  • 17
    • 35549006797 scopus 로고    scopus 로고
    • Sigma-1 receptor chaperones at the ERmitochondrion interface regulate Ca(2+) signaling and cell survival
    • Hayashi T, Su TP. Sigma-1 receptor chaperones at the ERmitochondrion interface regulate Ca(2+) signaling and cell survival. Cell 131, 596-610 (2007
    • (2007) Cell , vol.131 , pp. 596-610
    • Hayashi, T.1    Su, T.P.2
  • 18
    • 78449290844 scopus 로고    scopus 로고
    • The sigma-1 receptor chaperone as an inter-organelle signaling modulator
    • Su TP, Hayashi T, Maurice T et al. The sigma-1 receptor chaperone as an inter-organelle signaling modulator. Trends Pharmacol. Sci. 31, 557-566 (2010
    • (2010) Trends Pharmacol. Sci , vol.31 , pp. 557-566
    • Su, T.P.1    Hayashi, T.2    Maurice, T.3
  • 19
    • 79954498271 scopus 로고    scopus 로고
    • Targeting ligandoperated chaperone sigma-1 receptors in the treatment of neuropsychiatric disorders
    • Hayashi T, Tsai SY, Mori T et al. Targeting ligandoperated chaperone sigma-1 receptors in the treatment of neuropsychiatric disorders. Expert Opin. Ther. Targets 15, 557-577 (2011
    • (2011) Expert Opin. Ther. Targets , vol.15 , pp. 557-577
    • Hayashi, T.1    Tsai, S.Y.2    Mori, T.3
  • 20
    • 84887364156 scopus 로고    scopus 로고
    • The s-1 receptor interacts directly with GluN1 but not GluN2A in the GluN1/GluN2A NMDA receptor
    • Balasuriya D, Stewart AP, Edwardson JM. The s-1 receptor interacts directly with GluN1 but not GluN2A in the GluN1/GluN2A NMDA receptor. J. Neurosci., 33, 18219-18224 (2013
    • (2013) J. Neurosci , vol.33 , pp. 18219-18224
    • Balasuriya, D.1    Stewart, A.P.2    Edwardson, J.M.3
  • 21
    • 77950648247 scopus 로고    scopus 로고
    • Demonstration of a direct interaction between sigma-1 receptors and acid-sensing ion channels
    • Carnally SM, Johannessen M, Henderson RM et al. Demonstration of a direct interaction between sigma-1 receptors and acid-sensing ion channels. Biophys. J. 98, 1182-1191 (2010
    • (2010) Biophys. J. , vol.98 , pp. 1182-1191
    • Carnally, S.M.1    Johannessen, M.2    Henderson, R.M.3
  • 22
    • 77950226055 scopus 로고    scopus 로고
    • Sigma 1 receptor modulation of G-protein-coupled receptor signaling: Potentiation of opioid transduction independent from receptor binding
    • Kim FJ, Kovalyshyn I, Burgman M et al. Sigma 1 receptor modulation of G-protein-coupled receptor signaling: Potentiation of opioid transduction independent from receptor binding. Mol. Pharmacol. 77, 695-703 (2010
    • (2010) Mol. Pharmacol , vol.77 , pp. 695-703
    • Kim, F.J.1    Kovalyshyn, I.2    Burgman, M.3
  • 23
    • 84872567654 scopus 로고    scopus 로고
    • Dynamic interaction between sigma-1 receptor and Kv1.2 shapes neuronal and behavioral responses to cocaine
    • Kourrich S, Hayashi T, Chuang JY et al. Dynamic interaction between sigma-1 receptor and Kv1.2 shapes neuronal and behavioral responses to cocaine. Cell 152, 236-247 (2013
    • (2013) Cell , vol.152 , pp. 236-247
    • Kourrich, S.1    Hayashi, T.2    Chuang, J.Y.3
  • 24
    • 78649863658 scopus 로고    scopus 로고
    • Direct involvement of sigma-1 receptors in the dopamine D1 receptor-mediated effects of cocaine
    • Navarro G, Moreno E, Aymerich M et al. Direct involvement of sigma-1 receptors in the dopamine D1 receptor-mediated effects of cocaine. Proc Natl Acad Sci USA 107, 18676-18681 (2010
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 18676-18681
    • Navarro, G.1    Moreno, E.2    Aymerich, M.3
  • 25
    • 84876334881 scopus 로고    scopus 로고
    • Cocaine inhibits dopamine D2 receptor signaling via sigma-1-D2 receptor heteromers
    • Navarro G, Moreno E, Bonaventura J et al. Cocaine inhibits dopamine D2 receptor signaling via sigma-1-D2 receptor heteromers. PLoS ONE 8, e61245 (2013
    • (2013) PLoS ONE , vol.8
    • Navarro, G.1    Moreno, E.2    Bonaventura, J.3
  • 26
    • 56149083457 scopus 로고    scopus 로고
    • Sigma-1 receptor regulation of voltage-gated calcium channels involves a direct interaction
    • Tchedre KT, Huang RQ, Dibas A et al. Sigma-1 receptor regulation of voltage-gated calcium channels involves a direct interaction. Invest. Ophthalmol. Vis. Sci. 49, 4993-5002 (2008
    • (2008) Invest. Ophthalmol. Vis. Sci , vol.49 , pp. 4993-5002
    • Tchedre, K.T.1    Huang, R.Q.2    Dibas, A.3
  • 27
    • 37049016678 scopus 로고    scopus 로고
    • Sigma-1 receptors bind cholesterol and remodel lipid rafts in breast cancer cell lines
    • Palmer CP, Mahen R, Schnell E et al. Sigma-1 receptors bind cholesterol and remodel lipid rafts in breast cancer cell lines. Cancer Res. 67, 11166-11175 (2007
    • (2007) Cancer Res , vol.67 , pp. 11166-11175
    • Palmer, C.P.1    Mahen, R.2    Schnell, E.3
  • 28
    • 84891284846 scopus 로고    scopus 로고
    • Structure of the s1 receptor and its ligand binding site
    • Brune S, Pricl S, Wünsch B. Structure of the s1 receptor and its ligand binding site. J. Med. Chem. 56, 9809-9819 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 9809-9819
    • Brune, S.1    Pricl, S.2    Wünsch, B.3
  • 29
    • 0037171847 scopus 로고    scopus 로고
    • The sigma receptor as a ligand-regulated auxiliary potassium channel subunit
    • Aydar E, Palmer CP, Klyachko VA, Jackson MB. The sigma receptor as a ligand-regulated auxiliary potassium channel subunit. Neuron 34, 399-410 (2002
    • (2002) Neuron , vol.34 , pp. 399-410
    • Aydar, E.1    Palmer, C.P.2    Klyachko, V.A.3    Jackson, M.B.4
  • 30
    • 57649133946 scopus 로고    scopus 로고
    • Role of sigma-1 receptor C-Terminal segment in inositol 1 4, 5-Trisphosphate receptor activation: Constitutive enhancement of calcium signaling in MCF-7 tumor cells
    • Wu, Z.; Bowen, W. D. Role of sigma-1 receptor C-Terminal segment in inositol 1, 4, 5-Trisphosphate receptor activation: Constitutive enhancement of calcium signaling in MCF-7 tumor cells. J. Biol. Chem. 283, 28198-28215 (2008
    • (2008) J. Biol. Chem , Issue.283 , pp. 28198-28215
    • Wu, Z.1    Bowen, W.D.2
  • 31
    • 33947416579 scopus 로고    scopus 로고
    • Characterization of the cocaine binding site on the sigma-1 receptor
    • Chen Y, Hajipour AR, Sievert K et al. Characterization of the cocaine binding site on the sigma-1 receptor. Biochemistry 46, 3532-3542 (2007
    • (2007) Biochemistry , vol.46 , pp. 3532-3542
    • Chen, Y.1    Hajipour, A.R.2    Sievert, K.3
  • 32
    • 50349088217 scopus 로고    scopus 로고
    • Juxtaposition of the steroid binding domain-like i and II regions constitutes a ligand binding site in the s-1 receptor
    • Pal A, Chu UB, Ramachandran S et al. Juxtaposition of the steroid binding domain-like I and II regions constitutes a ligand binding site in the s-1 receptor. J. Biol. Chem. 283, 19646-19656 (2008
    • (2008) J. Biol. Chem , vol.283 , pp. 19646-19656
    • Pal, A.1    Chu, U.B.2    Ramachandran, S.3
  • 33
    • 46849119587 scopus 로고    scopus 로고
    • Probing the steroid binding domain-like i (SBDLI) of the sigma-1 receptor binding site using N-substituted photoaffinity labels
    • Fontanilla D, Hajipour AR, Pal A et al. Probing the steroid binding domain-like I (SBDLI) of the sigma-1 receptor binding site using N-substituted photoaffinity labels. Biochemistry 47, 7205-7217 (2008
    • (2008) Biochemistry , vol.47 , pp. 7205-7217
    • Fontanilla, D.1    Hajipour, A.R.2    Pal, A.3
  • 34
    • 0033040295 scopus 로고    scopus 로고
    • Amino acid residues in the transmembrane domain of the type 1 sigma receptor critical for ligand binding
    • Yamamoto H, Miura R, Yamamoto T et al. Amino acid residues in the transmembrane domain of the type 1 sigma receptor critical for ligand binding. FEBS Lett. 445, 19-22 (1999
    • (1999) FEBS Lett , vol.445 , pp. 19-22
    • Yamamoto, H.1    Miura, R.2    Yamamoto, T.3
  • 35
    • 0035948580 scopus 로고    scopus 로고
    • Expression pattern of the type 1 sigma receptor in the brain and identity of critical anionic amino acid residues in the ligand binding domain of the receptor
    • Seth P, Ganapathy ME, Conway SJ et al. Expression pattern of the type 1 sigma receptor in the brain and identity of critical anionic amino acid residues in the ligand binding domain of the receptor. Biochim. Biophys. Acta 1540, 59-67 (2001
    • (2001) Biochim. Biophys. Acta , vol.1540 , pp. 59-67
    • Seth, P.1    Ganapathy, M.E.2    Conway, S.J.3
  • 36
    • 84880529804 scopus 로고    scopus 로고
    • Characterization of the human sigma-1 receptor chaperone domain structure and binding immunoglobulin protein (BIP) interactions
    • Ortega-Roldan JL, Ossa F, Schnell JR. Characterization of the human sigma-1 receptor chaperone domain structure and binding immunoglobulin protein (BIP) interactions. J. Biol. Chem. 29, 21448-21457 (2013
    • (2013) J. Biol. Chem , vol.29 , pp. 21448-21457
    • Ortega-Roldan, J.L.1    Ossa, F.2    Schnell, J.R.3
  • 37
    • 84873347175 scopus 로고    scopus 로고
    • Photoaffinity labelling of the sigma-1 receptor with N-[3-(4-nitrophenyl) propyl]-N-dodecylamine: Evidence of receptor dimers
    • Chu UB, Ramachandran S, Hajipur A, Ruoho AE. Photoaffinity labelling of the sigma-1 receptor with N-[3-(4-nitrophenyl)propyl]-N-dodecylamine: Evidence of receptor dimers. Biochemistry 52, 859-868 (2013
    • (2013) Biochemistry , vol.52 , pp. 859-868
    • Chu, U.B.1    Ramachandran, S.2    Hajipur, A.3    Ruoho, A.E.4
  • 38
    • 84857132074 scopus 로고    scopus 로고
    • The ligand binding region of the sigma-1 receptor: Studies utilizing photoaffinity probes, sphingosine and N-Alkylamines
    • Ruoho AE, Chu UB, Ramachandran S et al. The ligand binding region of the sigma-1 receptor: Studies utilizing photoaffinity probes, sphingosine and N-Alkylamines. Curr. Pharm. Des. 18, 920-929 (2012
    • (2012) Curr. Pharm. des , vol.18 , pp. 920-929
    • Ruoho, A.E.1    Chu, U.B.2    Ramachandran, S.3
  • 39
    • 0028268389 scopus 로고
    • Structural features important for s1 receptor binding
    • Glennon RA, Ablordeppey SA, Ismaiel AM et al. Structural features important for s1 receptor binding. J. Med. Chem. 37, 1214-1219 (1994
    • (1994) J. Med. Chem , vol.37 , pp. 1214-1219
    • Glennon, R.A.1    Ablordeppey, S.A.2    Ismaiel, A.M.3
  • 40
    • 23844457000 scopus 로고    scopus 로고
    • Discovery of high-Affinity ligands of s1 receptor ERG2, and emopamil binding protein by pharmacophore modeling and virtual screening
    • Laggner C, Schieferer C, Fiechtner B et al. Discovery of high-Affinity ligands of s1 receptor, ERG2, and emopamil binding protein by pharmacophore modeling and virtual screening. J. Med. Chem. 48, 4754-4764 (2005
    • (2005) J. Med. Chem , vol.48 , pp. 4754-4764
    • Laggner, C.1    Schieferer, C.2    Fiechtner, B.3
  • 41
    • 69949100924 scopus 로고    scopus 로고
    • Syn thesis, biological evaluation, and three-dimensional in silico pharmacophore model for sigma 1) receptor ligands based on a series of substituted benzo-[d]oxazol-2(3H)-one derivatives
    • Zampieri D, Mamolo MG, Laurini E et al. Synthesis, biological evaluation, and three-dimensional in silico pharmacophore model for sigma (1) receptor ligands based on a series of substituted benzo-[d]oxazol-2(3H)-one derivatives. J. Med. Chem. 52, 5380-5393 (2009
    • (2009) J. Med. Chem , vol.52 , pp. 5380-5393
    • Zampieri, D.1    Mamolo, M.G.2    Laurini, E.3
  • 42
    • 84866348503 scopus 로고    scopus 로고
    • A s1 receptor pharmacophore derived from a series of N-substituted 4-Azahexacyclo[5.4.1.02 6.03, 10.05, 9.08, 11] dodecan-3-ols (AHDs)
    • Banister SD, Manoli M, Doddareddy MR et al. A s1 receptor pharmacophore derived from a series of N-substituted 4-Azahexacyclo[5.4.1.02, 6.03, 10.05, 9.08, 11] dodecan-3-ols (AHDs). Bioorg. Med. Chem. Lett. 22, 6053-6058 (2012
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , pp. 6053-6058
    • Banister, S.D.1    Manoli, M.2    Doddareddy, M.R.3
  • 43
    • 84855946245 scopus 로고    scopus 로고
    • Models of the pharmacophoric pattern and affinity trend of methyl 2-(aminomethyl)-1-phenylcyclopropane-1-carboxylate derivatives as s1 ligands
    • Caballero J, Zilocchi S, Tiznado W et al. Models of the pharmacophoric pattern and affinity trend of methyl 2-(aminomethyl)-1-phenylcyclopropane-1- carboxylate derivatives as s1 ligands. Mol. Simul. 38, 227-235 (2012
    • (2012) Mol. Simul , vol.38 , pp. 227-235
    • Caballero, J.1    Zilocchi, S.2    Tiznado, W.3
  • 44
    • 80955128570 scopus 로고    scopus 로고
    • Homology model and docking based virtual screening for ligands of the s1 receptor
    • Laurini E Col VD Mamolo MG et al. Homology model and docking based virtual screening for ligands of the s1 receptor. ACS Med. Chem. Lett. 2, 834-839 (2011
    • (2011) ACS Med. Chem. Lett , vol.2 , pp. 834-839
    • Laurini, E.1    Col, V.D.2    Mamolo, M.G.3
  • 45
    • 84868585563 scopus 로고    scopus 로고
    • Another brick in the wall Validation of the s1 receptor 3D model by computerassisted design, syn thesis, and activity of new s1 ligands
    • Laurini E, Marson D, Dal Col V et al. Another brick in the wall. Validation of the s1 receptor 3D model by computerassisted design, synthesis, and activity of new s1 ligands. Mol. Pharm. 9, 3107-3126 (2012
    • (2012) Mol. Pharm , vol.9 , pp. 3107-3126
    • Laurini, E.1    Marson, D.2    Dal Col, V.3
  • 46
    • 84883051500 scopus 로고    scopus 로고
    • Chemical, pharmacological, and in vitro metabolic stability studies on enantiomerically pure RC-33 compounds: Promising neuroprotective agents acting as s1 receptor agonists
    • Rossi D, Pedrali A, Gaggeri R et al. Chemical, pharmacological, and in vitro metabolic stability studies on enantiomerically pure RC-33 compounds: Promising neuroprotective agents acting as s1 receptor agonists. Chem. Med. Chem. 8, 1514-1527 (2013
    • (2013) Chem. Med. Chem , vol.8 , pp. 1514-1527
    • Rossi, D.1    Pedrali, A.2    Gaggeri, R.3
  • 47
    • 84874663522 scopus 로고    scopus 로고
    • 3D-QSAR and docking studies of pentacycloundecylamines at the sigma-1 (s 1) receptor
    • Geldenhuys WJ, Novotny, N, Malan SF et al. 3D-QSAR and docking studies of pentacycloundecylamines at the sigma-1 (s1) receptor. Bioorg. Med. Chem. Lett. 223, 1707-1711 (2013
    • (2013) Bioorg. Med. Chem. Lett , vol.223 , pp. 1707-1711
    • Geldenhuys, W.J.1    Novotny, N.2    Malan, S.F.3
  • 48
    • 84874304655 scopus 로고    scopus 로고
    • SKF83959 is a potent allosteric modulator of sigma-1 receptor
    • Guo L, Zhao J, Jin G et al. SKF83959 is a potent allosteric modulator of sigma-1 receptor. Mol. Pharm. 83, 577-586 (2013
    • (2013) Mol. Pharm , vol.83 , pp. 577-586
    • Guo, L.1    Zhao, J.2    Jin, G.3
  • 49
    • 84876666233 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-(5-methyl-4-phenyl-2- oxopyrrolidin-1-yl)-Acetamide stereoisomers as novel positive allosteric modulators of sigma-1 receptor
    • Veinberg G, Vorona M, Zvejniece L et al. Synthesis and biological evaluation of 2-(5-methyl-4-phenyl-2-oxopyrrolidin-1-yl)-Acetamide stereoisomers as novel positive allosteric modulators of sigma-1 receptor. Bioorg. Med. Chem. 21, 2764-2771 (2013
    • (2013) Bioorg. Med. Chem , vol.21 , pp. 2764-2771
    • Veinberg, G.1    Vorona, M.2    Zvejniece, L.3
  • 50
    • 80055001170 scopus 로고    scopus 로고
    • The dipeptide Phe-Phe amide attenuates signs of hyperalgesia, allodynia and nociception in diabetic mice using a mechanism involving the sigma receptor system
    • Ohsawa M, Carlsson A, Asato M et al. The dipeptide Phe-Phe amide attenuates signs of hyperalgesia, allodynia and nociception in diabetic mice using a mechanism involving the sigma receptor system. Mol. Pain 7, 85 (2011
    • (2011) Mol. Pain , vol.7 , Issue.85
    • Ohsawa, M.1    Carlsson, A.2    Asato, M.3
  • 52
    • 84860889919 scopus 로고    scopus 로고
    • Sigma-1 receptor chaperones regulate the secretion of brain-derived neurotrophic factor
    • Fujimoto M, Hayashi T, Urfer R et al. Sigma-1 receptor chaperones regulate the secretion of brain-derived neurotrophic factor. Synapse 66, 630-639 (2012
    • (2012) Synapse , vol.66 , pp. 630-639
    • Fujimoto, M.1    Hayashi, T.2    Urfer, R.3
  • 54
    • 80051958777 scopus 로고    scopus 로고
    • Anti-Amnesic and neuroprotective potentials of the mixed muscarinic receptor/sigma1 (s 1) ligand ANAVEX2-73, a novel aminotetrahydrofuran derivative
    • Villard V, Espallergues J, Keller E et al. Anti-Amnesic and neuroprotective potentials of the mixed muscarinic receptor/sigma1 (s1) ligand ANAVEX2-73, a novel aminotetrahydrofuran derivative. J. Psychopharm. 25, 1101-1117 (2011
    • (2011) J. Psychopharm , vol.25 , pp. 1101-1117
    • Villard, V.1    Espallergues, J.2    Keller, E.3
  • 55
    • 84876131740 scopus 로고    scopus 로고
    • Identification of RC-33 as a potent and selective s1 receptor agonist potentiating NGF-induced neurite outgrowth in PC12 cells Part 2: GScale syn thesis, physicochemical characterization and in vitro metabolic stability
    • Rossi D, Marra A, Picconi P et al. Identification of RC-33 as a potent and selective s1 receptor agonist potentiating NGF-induced neurite outgrowth in PC12 cells. Part 2: GScale synthesis, physicochemical characterization and in vitro metabolic stability. Bioorg. Med. Chem. 21, 2577-2586 (2013
    • (2013) Bioorg. Med. Chem , vol.21 , pp. 2577-2586
    • Rossi, D.1    Marra, A.2    Picconi, P.3
  • 56
    • 84868021206 scopus 로고    scopus 로고
    • Sigma-1R agonist improves motor function and motoneuron survival in ALS mice
    • Mancuso R, Olivan S, Rando A et al. Sigma-1R agonist improves motor function and motoneuron survival in ALS mice. Neurotherapeutics 9, 814-826 (2012
    • (2012) Neurotherapeutics , vol.9 , pp. 814-826
    • Mancuso, R.1    Olivan, S.2    Rando, A.3
  • 57
    • 84877298835 scopus 로고    scopus 로고
    • Crucial interactions between selective serotonin uptake inhibitors and sigma-1 receptor in heart failure
    • Bhuiyan MS, Tagashira H, Fukunaga K. Crucial interactions between selective serotonin uptake inhibitors and sigma-1 receptor in heart failure. J. Pharmacol. Sci. 121, 177-184 (2013
    • (2013) J. Pharmacol. Sci , vol.121 , pp. 177-184
    • Bhuiyan, M.S.1    Tagashira, H.2    Fukunaga, K.3
  • 60
    • 78649964052 scopus 로고    scopus 로고
    • Sigma receptors in oncology: Therapeutic and diagnostic applications of sigma ligands
    • van Waarde A, Rybczynska AA, Ramakrishnan N et al. Sigma receptors in oncology: Therapeutic and diagnostic applications of sigma ligands. Curr. Pharm. Des. 16, 3519-3537 (2010
    • (2010) Curr. Pharm. des , vol.16 , pp. 3519-3537
    • Van Waarde, A.1    Rybczynska, A.A.2    Ramakrishnan, N.3
  • 61
    • 0028930208 scopus 로고
    • Sigma antagonists potentiate opioid analgesia in rats
    • Chien CC, Pasternak GW. Sigma antagonists potentiate opioid analgesia in rats. Neurosci. Lett. 190, 137-139 (1995
    • (1995) Neurosci. Lett , vol.190 , pp. 137-139
    • Chien, C.C.1    Pasternak, G.W.2
  • 62
    • 1642463533 scopus 로고    scopus 로고
    • Generation and phenotypic analysis of sigma receptor type i (sigma 1) knockout mice
    • Langa F, Codony X, Tovar V et al. Generation and phenotypic analysis of sigma receptor type I (sigma 1) knockout mice. Eur. J. Neurosci. 18, 2188-2196 (2003
    • (2003) Eur. J. Neurosci , vol.18 , pp. 2188-2196
    • Langa, F.1    Codony, X.2    Tovar, V.3
  • 63
    • 69249149994 scopus 로고    scopus 로고
    • Selective sigma-1 (sigma1) receptor antagonists: Emerging target for the treatment of neuropathic pain
    • Diaz JL, Zamanillo D, Corbera J et al. Selective sigma-1 (sigma1) receptor antagonists: Emerging target for the treatment of neuropathic pain. Cent. Nerv. Syst. Agents Med. Chem. 9, 172-183 (2009
    • (2009) Cent. Nerv. Syst. Agents Med. Chem , vol.9 , pp. 172-183
    • Diaz, J.L.1    Zamanillo, D.2    Corbera, J.3
  • 64
    • 69649104522 scopus 로고    scopus 로고
    • Sigma-1 receptors regulate activity-induced spinal sensitization and neuropathic pain after peripheral nerve injury
    • de la Puente B, Nadal X, Portillo-Salido E et al. Sigma-1 receptors regulate activity-induced spinal sensitization and neuropathic pain after peripheral nerve injury. Pain 145, 294-303 (2009
    • (2009) Pain , vol.145 , pp. 294-303
    • De La Puente, B.1    Nadal, X.2    Portillo-Salido, E.3
  • 65
    • 67349154763 scopus 로고    scopus 로고
    • Sigma-1 receptors are essential for capsaicin-induced mechanical hypersensitivity: Studies with selective sigma-1 ligands and sigma-1 knockout mice
    • Entrena JM, Cobos EJ, Nieto FR et al. Sigma-1 receptors are essential for capsaicin-induced mechanical hypersensitivity: Studies with selective sigma-1 ligands and sigma-1 knockout mice. Pain 143, 252-261 (2009
    • (2009) Pain , vol.143 , pp. 252-261
    • Entrena, J.M.1    Cobos, E.J.2    Nieto, F.R.3
  • 66
    • 15044338830 scopus 로고    scopus 로고
    • Formalininduced pain is reduced in sigma-1 receptor knockout mice
    • Cendan CM, Pujalte JM, Portillo-Salido E et al. Formalininduced pain is reduced in sigma-1 receptor knockout mice. Eur. J. Pharmacol. 511, 73-74, (2005
    • (2005) Eur. J. Pharmacol , vol.511 , pp. 73-74
    • Cendan, C.M.1    Pujalte, J.M.2    Portillo-Salido, E.3
  • 67
    • 84868203235 scopus 로고    scopus 로고
    • Role of sigma-1 receptors in paclitaxel-induced neuropathic pain in mice
    • Nieto FR, Cendan CM, Sánchez-Fernández C et al. Role of sigma-1 receptors in paclitaxel-induced neuropathic pain in mice. J. Pain 13, 1107-1121 (2012
    • (2012) J. Pain , vol.13 , pp. 1107-1121
    • Nieto, F.R.1    Cendan, C.M.2    Sánchez-Fernández, C.3
  • 68
    • 84874654899 scopus 로고    scopus 로고
    • S 1 receptors are involved in the visceral pain induced by intracolonic administration of capsaicin in mice
    • Gonzαlez-Cano R, Merlos M, Baeyens JM Cendαn CM. s1 receptors are involved in the visceral pain induced by intracolonic administration of capsaicin in mice. Anesthesiology 118, 691-700 (2013
    • (2013) Anesthesiology , vol.118 , pp. 691-700
    • González-Cano, R.1    Merlos, M.2    Baeyens, J.M.3    Cendán, C.M.4
  • 69
    • 33745101432 scopus 로고    scopus 로고
    • Intrathecal treatment with sigma-1 receptor antagonists reduces formalininduced phosphorylation of NMDA receptor subunit 1 and the second phase of formalin test in mice
    • Kim HW, Kwon YB, Roh DH et al. Intrathecal treatment with sigma-1 receptor antagonists reduces formalininduced phosphorylation of NMDA receptor subunit 1 and the second phase of formalin test in mice. Br. J. Pharmacol. 148, 490-498 (2006
    • (2006) Br. J. Pharmacol , vol.148 , pp. 490-498
    • Kim, H.W.1    Kwon, Y.B.2    Roh, D.H.3
  • 70
    • 56149124983 scopus 로고    scopus 로고
    • Intrathecal injection of the sigma(1) receptor antagonist BD1047 blocks both mechanical allodynia and increases in spinal NR1 expression during the induction phase of rodent neuropathic pain
    • Roh DH, Kim HW, Yoon SY et al. Intrathecal injection of the sigma(1) receptor antagonist BD1047 blocks both mechanical allodynia and increases in spinal NR1 expression during the induction phase of rodent neuropathic pain. Anesthesiology 109, 879-889 (2008
    • (2008) Anesthesiology , vol.109 , pp. 879-889
    • Roh, D.H.1    Kim, H.W.2    Yoon, S.Y.3
  • 71
    • 79251492697 scopus 로고    scopus 로고
    • Sigma-1 receptor antagonist BD1047 reduces allodynia and spinal ERK phosphorylation following chronic compression of dorsal root ganglion in rats
    • Son JS, Kwon YB. Sigma-1 receptor antagonist BD1047 reduces allodynia and spinal ERK phosphorylation following chronic compression of dorsal root ganglion in rats. Korean. J. Physiol. Pharmacol. 14, 359-364 (2010
    • (2010) Korean. J. Physiol. Pharmacol , vol.14 , pp. 359-364
    • Son, J.S.1    Kwon, Y.B.2
  • 72
    • 75749096775 scopus 로고    scopus 로고
    • The antinociceptive effect of sigma-1 receptor antagonist, BD1047, in a capsaicin induced headache model in rats
    • Kwon YB, Jeong YC, Kwon JK et al. The antinociceptive effect of sigma-1 receptor antagonist, BD1047, in a capsaicin induced headache model in rats. Korean. J. Physiol. Pharmacol. 13, 425-429 (2009
    • (2009) Korean. J. Physiol. Pharmacol , vol.13 , pp. 425-429
    • Kwon, Y.B.1    Jeong, Y.C.2    Kwon, J.K.3
  • 73
    • 84881372529 scopus 로고    scopus 로고
    • Sigma-1 receptormediated increase in spinal p38 MAPK phosphorylation leads to the induction of mechanical allodynia in mice and neuropathic rats
    • Moon JY, Roh DH, Yoon SY et al. Sigma-1 receptormediated increase in spinal p38 MAPK phosphorylation leads to the induction of mechanical allodynia in mice and neuropathic rats. Exp. Neurol. 247, 383-391 (2013
    • (2013) Exp. Neurol , vol.247 , pp. 383-391
    • Moon, J.Y.1    Roh, D.H.2    Yoon, S.Y.3
  • 74
    • 80052470110 scopus 로고    scopus 로고
    • Progesterone prevents development of neuropathic pain in a rat model: Timing and duration of treatment are critical
    • Dableh LJ, Henry JL. Progesterone prevents development of neuropathic pain in a rat model: Timing and duration of treatment are critical. J. Pain Res. 4, 91-101 (2011
    • (2011) J. Pain Res , vol.4 , pp. 91-101
    • Dableh, L.J.1    Henry, J.L.2
  • 75
    • 84885469060 scopus 로고    scopus 로고
    • Agmatine attenuates neuropathic pain in sciatic nerve ligated rats: Modulation by hippocampal sigma receptors
    • Kotagale NR, Shirbhate SH, Shukla P, Ugale RR. Agmatine attenuates neuropathic pain in sciatic nerve ligated rats: Modulation by hippocampal sigma receptors. Eur. J. Pharmacol. 714, 424-431 (2013
    • (2013) Eur. J. Pharmacol , vol.714 , pp. 424-431
    • Kotagale, N.R.1    Shirbhate, S.H.2    Shukla, P.3    Ugale, R.R.4
  • 76
    • 84867387612 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of the 1-Arylpyrazole class of s1 receptor antagonists: Identification of 4-{2-[5-methyl-1-(naphthalen-2-yl)-1H- pyrazol-3-yloxy]ethyl}morpholine (S1RA, E-52862
    • Dénaz JL, Cuberes R, Berrocal J et al. Synthesis and biological evaluation of the 1-Arylpyrazole class of s1 receptor antagonists: Identification of 4-{2-[5-methyl-1-(naphthalen-2-yl)-1H-pyrazol-3-yloxy]ethyl} morpholine (S1RA, E-52862). J. Med. Chem. 55, 8211-8224 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 8211-8224
    • Díaz, J.L.1    Cuberes, R.2    Berrocal, J.3
  • 77
    • 84864447546 scopus 로고    scopus 로고
    • Pharmacological properties of S1RA, a new sigma-1 receptor antagonist that inhibits neuropathic pain and activity-induced spinal sensitization
    • Romero L, Zamanillo D, Nadal X et al. Pharmacological properties of S1RA, a new sigma-1 receptor antagonist that inhibits neuropathic pain and activity-induced spinal sensitization. Br. J. Pharmacol. 166, 2289-2306 (2012
    • (2012) Br. J. Pharmacol , vol.166 , pp. 2289-2306
    • Romero, L.1    Zamanillo, D.2    Nadal, X.3
  • 78
    • 84879586305 scopus 로고    scopus 로고
    • Operant selfadministration of a sigma ligand improves nociceptive and emotional manifestations of neuropathic pain
    • Bura AS, Guegan T, Zamanillo D et al. Operant selfadministration of a sigma ligand improves nociceptive and emotional manifestations of neuropathic pain. Eur. J. Pain. 17, 832-843 (2013
    • (2013) Eur. J. Pain , vol.17 , pp. 832-843
    • Bura, A.S.1    Guegan, T.2    Zamanillo, D.3
  • 79
    • 84878163668 scopus 로고    scopus 로고
    • Sigma-1 receptor antagonism as opioid adjuvant strategy: Enhancement of opioid antinociception without increasing adverse effects
    • Vidal-Torres A, de la Puente B, Rocasalbas M et al. Sigma-1 receptor antagonism as opioid adjuvant strategy: Enhancement of opioid antinociception without increasing adverse effects. Eur. J. Pharmacol. 711, 63-72 (2013
    • (2013) Eur. J. Pharmacol , vol.711 , pp. 63-72
    • Vidal-Torres, A.1    De La Puente, B.2    Rocasalbas, M.3
  • 80
    • 84876998778 scopus 로고    scopus 로고
    • Potentiation of morphine-induced mechanical antinociception by s1 receptor inhibition: Role of peripheral s1 receptors
    • Sαnchez-Fernαndez C, Nieto FR, Gonzαlez-Cano R et al. Potentiation of morphine-induced mechanical antinociception by s1 receptor inhibition: Role of peripheral s1 receptors. Neuropharmacology 70, 348-358 (2013
    • (2013) Neuropharmacology , vol.70 , pp. 348-358
    • Sánchez-Fernández, C.1    Nieto, F.R.2    González-Cano, R.3
  • 81
    • 84867385161 scopus 로고    scopus 로고
    • Safety, tolerability and pharmacokinetics of single and multiple doses of a novel sigma-1 receptor antagonist in three randomized phase i studies
    • Abadias M, Escriche M, Vaqué A et al. Safety, tolerability and pharmacokinetics of single and multiple doses of a novel sigma-1 receptor antagonist in three randomized phase I studies. Br. J. Clin. Pharmacol. 75, 103-117 (2013
    • (2013) Br. J. Clin. Pharmacol , vol.75 , pp. 103-117
    • Abadias, M.1    Escriche, M.2    Vaqué, A.3
  • 82
    • 84905476422 scopus 로고    scopus 로고
    • Esteve. www.esteve.es
    • Esteve
  • 83
    • 84867340616 scopus 로고    scopus 로고
    • The s1 receptor antagonist S1RA is a promising candidate for the treatment of neurogenic pain
    • Wünsch B. The s1 receptor antagonist S1RA is a promising candidate for the treatment of neurogenic pain. J. Med. Chem. 55, 8209-8210 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 8209-8210
    • Wünsch, B.1
  • 84
    • 84879590779 scopus 로고    scopus 로고
    • Assessment of the sigma-1 receptor antagonist (S1RA): A model approach for preclinical analgesic drug discovery
    • Neubert J. Assessment of the sigma-1 receptor antagonist (S1RA): A model approach for preclinical analgesic drug discovery. Eur. J. Pain. 17, 789-790 (2013
    • (2013) Eur. J. Pain , vol.17 , pp. 789-790
    • Neubert, J.1
  • 85
    • 84861096654 scopus 로고    scopus 로고
    • Crystal structure of the opioid receptor bound to a morphinan antagonist
    • Manglik A, Kruse AC, Kobilka TS et al. Crystal structure of the opioid receptor bound to a morphinan antagonist. Nature 485, 321-326 (2012
    • (2012) Nature , vol.485 , pp. 321-326
    • Manglik, A.1    Kruse, A.C.2    Kobilka, T.S.3
  • 86
    • 33746280830 scopus 로고    scopus 로고
    • A medicinal chemistry guided approach to selective and drug-like sigma 1 ligands
    • Corbera J, Vaño D, Martínez D et al. A medicinal chemistry guided approach to selective and drug-like sigma 1 ligands. Chem. Med. Chem. 1, 140-154 (2006
    • (2006) Chem. Med. Chem , vol.1 , pp. 140-154
    • Corbera, J.1    Vaño, D.2    Martínez, D.3
  • 87
    • 77749315417 scopus 로고    scopus 로고
    • Lipophilicity in drug discovery
    • Waring MJ. Lipophilicity in drug discovery. Expert Opin. Drug Discov. 5, 235-248 (2010
    • (2010) Expert Opin. Drug Discov , vol.5 , pp. 235-248
    • Waring, M.J.1
  • 88
    • 82255175450 scopus 로고    scopus 로고
    • Synthesis and binding assays of novel 3, 3-dimethylpiperidine derivatives with various lipophilicities as s1 receptor ligands
    • Ferorelli S, Abate C, Pedone MP et al. Synthesis and binding assays of novel 3, 3-dimethylpiperidine derivatives with various lipophilicities as s1 receptor ligands. Bioorg. Med. Chem. 19, 7612-7623 (2011
    • (2011) Bioorg. Med. Chem , vol.19 , pp. 7612-7623
    • Ferorelli, S.1    Abate, C.2    Pedone, M.P.3
  • 89
    • 84876671257 scopus 로고    scopus 로고
    • Analysis of the molecular interactions of the potent analgesic s1ra with the s1 receptor
    • Laurini E, Dal Col V, Wünsch B, Pricl S. Analysis of the molecular interactions of the potent analgesic S1RA with the s1 receptor. Bioorg. Med. Chem. Lett. 23, 2868-2871 (2013
    • (2013) Bioorg. Med. Chem. Lett , vol.23 , pp. 2868-2871
    • Laurini, E.1    Dal Col, V.2    Wünsch, B.3    Pricl, S.4
  • 90
    • 33645958854 scopus 로고    scopus 로고
    • In vivo evaluation of (+)-MR200 as a new selective sigma ligand modulating MOP, DOP and KOP supraspinal analgesia
    • Marrazzo A, Parenti C, Scavo V et al. In vivo evaluation of (+)-MR200 as a new selective sigma ligand modulating MOP, DOP and KOP supraspinal analgesia. Life Sci. 78, 2449-2453 (2006
    • (2006) Life Sci , vol.78 , pp. 2449-2453
    • Marrazzo, A.1    Parenti, C.2    Scavo, V.3
  • 91
    • 79957715076 scopus 로고    scopus 로고
    • Novel potent and selective s ligands: Evaluation of their agonist and antagonist properties
    • Marrazzo A, Cobos EJ, Parenti C et al. Novel potent and selective s ligands: Evaluation of their agonist and antagonist properties. J. Med. Chem. 54, 3669-3673 (2011
    • (2011) J. Med. Chem , vol.54 , pp. 3669-3673
    • Marrazzo, A.1    Cobos, E.J.2    Parenti, C.3
  • 92
    • 84900360607 scopus 로고    scopus 로고
    • Effects of a selective sigma 1 antagonist compound on inflammatory pain
    • Parent C, Marrazzo A, Aricò G et al. Effects of a selective sigma 1 antagonist compound on inflammatory pain. Inflammation 37(1), 261-266 (2013
    • (2013) Inflammation , vol.37 , Issue.1 , pp. 261-266
    • Parent, C.1    Marrazzo, A.2    Aricò, G.3
  • 93
    • 84877686385 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a new series of hexahydro-2Hpyrano[3 2-c]quinolines as novel selective s1 receptor ligands
    • Díaz JL, Christmann U, Fernández A et al. Synthesis and biological evaluation of a new series of hexahydro-2Hpyrano 3, 2-c]quinolines as novel selective s1 receptor ligands. J. Med. Chem. 56, 3656-3665 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 3656-3665
    • Díaz, J.L.1    Christmann, U.2    Fernández, A.3
  • 94
    • 79960159022 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of a potent and selective s1 receptor antagonist with high antiallodynic activity
    • Utech T, Kfhler J, Buschmann H et al. Synthesis and pharmacological evaluation of a potent and selective s1 receptor antagonist with high antiallodynic activity. Arch. Pharm. Chem. Life Sci. 344, 415-421 (2011
    • (2011) Arch. Pharm. Chem. Life Sci , vol.344 , pp. 415-421
    • Utech, T.1    Köhler, J.2    Buschmann, H.3
  • 95
    • 79955580441 scopus 로고    scopus 로고
    • Synthesis of 4-(aminoalkyl) substituted 1, 3-dioxanes as potent NMDA and s receptor antagonists
    • Utech T, Kfhler J, Wünsch B. Synthesis of 4-(aminoalkyl) substituted 1, 3-dioxanes as potent NMDA and s receptor antagonists. Eur. J. Med. Chem. 46, 2157-2169 (2011
    • (2011) Eur. J. Med. Chem , vol.46 , pp. 2157-2169
    • Utech, T.1    Köhler, J.2    Wünsch, B.3
  • 96
    • 65349124943 scopus 로고    scopus 로고
    • Pharmacological and metabolic characterisation of the potent s1 receptor ligand 10-benzyl-3-methoxy-3H-spiro[[2]benzofuran-1, 4-piperidine
    • Wiese C, Maestrup EG, Schepmann D et al. Pharmacological and metabolic characterisation of the potent s1 receptor ligand 10-benzyl-3-methoxy-3H- spiro[[2]benzofuran-1, 4-piperidine]. J. Pharm. Pharmacology 61, 631-640 (2009
    • (2009) J Pharm. Pharmacology , vol.61 , pp. 631-640
    • Wiese, C.1    Maestrup, E.G.2    Schepmann, D.3
  • 97
    • 80053900174 scopus 로고    scopus 로고
    • Combination of two pharmacophoric systems: Synthesis and pharmacological evaluation of spirocyclic pyranopyrazoles with high s1 receptor affinity
    • Schldger T, Schepmann D, Lehmkuhl K et al. Combination of two pharmacophoric systems: Synthesis and pharmacological evaluation of spirocyclic pyranopyrazoles with high s1 receptor affinity. J. Med. Chem. 54, 6704-6713 (2011
    • (2011) J. Med. Chem , vol.54 , pp. 6704-6713
    • Schlöger, T.1    Schepmann, D.2    Lehmkuhl, K.3
  • 98
    • 54549085666 scopus 로고    scopus 로고
    • Thiophene bioisosteres of spirocyclic s receptor ligands 1 N-Substituted spiro[piperidine-4, 4'-Thieno[3, 2-c]pyrans]
    • Oberdorf C, Schepmann D, Vela JM et al. Thiophene bioisosteres of spirocyclic s receptor ligands. 1. N-Substituted spiro[piperidine-4, 4'-Thieno[3, 2-c]pyrans]. J. Med. Chem. 51, 6531-6537 (2008
    • (2008) J. Med. Chem , Issue.51 , pp. 6531-6537
    • Oberdorf, C.1    Schepmann, D.2    Vela, J.M.3
  • 99
    • 84862285956 scopus 로고    scopus 로고
    • Thiophene bioisosteres of spirocyclic s receptor ligands: Relationships between substitution pattern and s receptor affinity
    • Oberdorf C, Schepmann D, Vela JM et al. Thiophene bioisosteres of spirocyclic s receptor ligands: Relationships between substitution pattern and s receptor affinity. J. Med. Chem. 55, 5350-5360 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 5350-5360
    • Oberdorf, C.1    Schepmann, D.2    Vela, J.M.3
  • 100
    • 84866856929 scopus 로고    scopus 로고
    • Pd-Catalyzed direct C-H bond functionalization of spirocyclic s1 ligands: Generation of a pharmacophore model and analysis of the reverse binding mode by docking into a 3D homology model of the s1 receptor
    • Meyer C, Schepmann D, Yanagisawa S et al. Pd-Catalyzed direct C-H bond functionalization of spirocyclic s1 ligands: Generation of a pharmacophore model and analysis of the reverse binding mode by docking into a 3D homology model of the s1 receptor. J. Med. Chem. 55, 8047-8065 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 8047-8065
    • Meyer, C.1    Schepmann, D.2    Yanagisawa, S.3
  • 101
    • 84875212566 scopus 로고    scopus 로고
    • Improvement of s1 receptor affinity by late-stage C-H-bond arylation of spirocyclic lactones Bioorg
    • Meyer C, Neue B, Schepmann D et al. Improvement of s1 receptor affinity by late-stage C-H-bond arylation of spirocyclic lactones Bioorg. Med. Chem. 21, 1844-1856 (2013
    • (2013) Med. Chem , vol.21 , pp. 1844-1856
    • Meyer, C.1    Neue, B.2    Schepmann, D.3
  • 102
    • 84857126465 scopus 로고    scopus 로고
    • Pharmacophore models and development of spirocyclic ligands for s1 receptors
    • Wünsch B. Pharmacophore models and development of spirocyclic ligands for s1 receptors. Curr. Pharm. Des. 18, 930-937 (2012
    • (2012) Curr. Pharm. des , vol.18 , pp. 930-937
    • Wünsch, B.1
  • 103
    • 84863734437 scopus 로고    scopus 로고
    • New adamantane derivatives with sigma affinity and antiproliferative activity
    • Riganas S, Papanastasiou J, Foscolos GB et al. New adamantane derivatives with sigma affinity and antiproliferative activity. Med. Chem. 8, 569-586 (2012
    • (2012) Med. Chem , vol.8 , pp. 569-586
    • Riganas, S.1    Papanastasiou, J.2    Foscolos, G.B.3
  • 104
    • 84860466359 scopus 로고    scopus 로고
    • Syn thesis, s 1, s2-receptors binding affinity and antiproliferative action of new C1-substituted adamantanes
    • Riganas S, Papanastasiou J, Foscolos GB et al. Synthesis, s1, s2-receptors binding affinity and antiproliferative action of new C1-substituted adamantanes. Bioorg. Med. Chem. 20, 3323-3331 (2012
    • (2012) Bioorg. Med. Chem , vol.20 , pp. 3323-3331
    • Riganas, S.1    Papanastasiou, J.2    Foscolos, G.B.3
  • 105
    • 84870021399 scopus 로고    scopus 로고
    • New adamantane phenylalkylamines with s-receptor binding affinity and anticancer activity, associated with putative antagonism of neuropathic pain
    • Riganas S, Papanastasiou J, Foscolos GB et al. New adamantane phenylalkylamines with s-receptor binding affinity and anticancer activity, associated with putative antagonism of neuropathic pain. J. Med. Chem. 55, 10241-10261 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 10241-10261
    • Riganas, S.1    Papanastasiou, J.2    Foscolos, G.B.3
  • 106
    • 84905476410 scopus 로고    scopus 로고
    • Mochida Pharmaceutical Co. Ltd WO2006118307
    • Mochida Pharmaceutical Co. Ltd: Therapeutic agent for pain. WO2006118307 (2006
    • (2006) Therapeutic Agent for Pain
  • 107
    • 84905476411 scopus 로고    scopus 로고
    • 8 th AFMC International Medicinal Chemistry Symposium". 29 November-2 December, Tokyo, Japan, Abstract 2P-132
    • 8th AFMC International Medicinal Chemistry Symposium" Frontier of Medicinal Science". 29 November-2 December, Tokyo, Japan, Abstract 2P-132 (2011
    • (2011) Frontier of Medicinal Science
  • 109
    • 84877979541 scopus 로고    scopus 로고
    • The evaluation of AZ66, an optimized sigma receptor antagonist, against methamphetamine-induced dopaminergic neurotoxicity and memory impairment in mice
    • Seminerio MJ, Hansen R, Kaushal N et al. The evaluation of AZ66, an optimized sigma receptor antagonist, against methamphetamine-induced dopaminergic neurotoxicity and memory impairment in mice. Int. J. Neuropsychopharm. 16, 1033-1044 (2013
    • (2013) Int. J. Neuropsychopharm , vol.16 , pp. 1033-1044
    • Seminerio, M.J.1    Hansen, R.2    Kaushal, N.3
  • 110
    • 84881371612 scopus 로고    scopus 로고
    • Effect of ringconstrained phenylpropyloxyethylamines on sigma receptors
    • Stavitskaya L, Seminerio MJ, Healy JR et al. Effect of ringconstrained phenylpropyloxyethylamines on sigma receptors. Bioorg. Med. Chem. 21, 4923-4927 (2013
    • (2013) Bioorg. Med. Chem , vol.21 , pp. 4923-4927
    • Stavitskaya, L.1    Seminerio, M.J.2    Healy, J.R.3
  • 111
    • 84877647740 scopus 로고    scopus 로고
    • Synthesis and receptor binding studies of novel 4, 4-disubstituted arylalkyl/arylalkylsulfonyl piperazine and piperidine-based derivatives as a new class of s1 ligands
    • Sadeghzadeh M, Sheibani S, Ghandi M et al. Synthesis and receptor binding studies of novel 4, 4-disubstituted arylalkyl/arylalkylsulfonyl piperazine and piperidine-based derivatives as a new class of s1 ligands. Eur. J. Med. Chem. 64, 488-497 (2013
    • (2013) Eur. J. Med. Chem , vol.64 , pp. 488-497
    • Sadeghzadeh, M.1    Sheibani, S.2    Ghandi, M.3
  • 112
    • 84871228559 scopus 로고    scopus 로고
    • From α4β2 nicotinic ligands to the discovery of s1 receptor ligands: Pharmacophore analysis and rational design
    • Yu LF, Zhang HK, Gunosewoyo H, Kozikowski AP. From α4β2 nicotinic ligands to the discovery of s1 receptor ligands: Pharmacophore analysis and rational design. ACS. Med. Chem. Lett. 3, 1054-1058 (2012
    • (2012) ACS. Med. Chem. Lett , vol.3 , pp. 1054-1058
    • Yu, L.F.1    Zhang, H.K.2    Gunosewoyo, H.3    Kozikowski, A.P.4
  • 113
    • 84881377350 scopus 로고    scopus 로고
    • Structure activity relationship study of benzo[d]thiazol-2(3H)one based s receptor ligands
    • Bhat R, Fishback JA, Matsumoto RR et al. Structure activity relationship study of benzo[d]thiazol-2(3H)one based s receptor ligands. Bioorg. Med. Chem. Lett. 23, 5011-5013 (2013
    • (2013) Bioorg. Med. Chem. Lett , vol.23 , pp. 5011-5013
    • Bhat, R.1    Fishback, J.A.2    Matsumoto, R.R.3
  • 114
    • 84867338447 scopus 로고    scopus 로고
    • New positron emission tomography (PET) radioligand for imaging s1 receptors in living subjects
    • James ML, Shen B, Zavaleta CL et al. New positron emission tomography (PET) radioligand for imaging s1 receptors in living subjects. J. Med. Chem. 55, 8272-8282 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 8272-8282
    • James, M.L.1    Shen, B.2    Zavaleta, C.L.3
  • 115
    • 84883454022 scopus 로고    scopus 로고
    • N-substituted 8-Aminopentacyclo[5.4.0.02 6.03, 10.05, 9]undecanes as s receptor ligands with potential neuroprotective effects
    • Banister SD, Manoli M, Barron ML et al. N-substituted 8-Aminopentacyclo[5.4.0.02, 6.03, 10.05, 9]undecanes as s receptor ligands with potential neuroprotective effects. Bioorg. Med. Chem. 21, 6038-6052 (2013
    • (2013) Bioorg. Med. Chem , vol.21 , pp. 6038-6052
    • Banister, S.D.1    Manoli, M.2    Barron, M.L.3
  • 116
    • 84861576092 scopus 로고    scopus 로고
    • 7-Azabicyclo[2.2.1] heptane as a scaffold for the of selective sigma-2 (s 2) receptor ligands. Bioorg
    • Banister SD, Rendina LM, Kassiou M. 7-Azabicyclo[2.2.1]heptane as a scaffold for the development of selective sigma-2 (s2) receptor ligands. Bioorg. Med. Chem. Lett. 22, 4059-4063 (2012
    • (2012) Med. Chem. Lett , vol.22 , pp. 4059-4063
    • Banister, S.D.1    Rendina, L.M.2    Kassiou, M.3
  • 117
    • 84865132513 scopus 로고    scopus 로고
    • Exploration of ring size in a series of cyclic vicinal diamines with s1 receptor affinity
    • Moussa IA, Banister SD, Manoli M et al. Exploration of ring size in a series of cyclic vicinal diamines with s1 receptor affinity. Bioorg. Med. Chem. Lett. 22, 5493-5497 (2012
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , pp. 5493-5497
    • Moussa, I.A.1    Banister, S.D.2    Manoli, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.