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Volumn 86, Issue 3, 2014, Pages 342-357

New positive Ca2+-activated K+ channel gating modulators with selectivity for KCa3.1

Author keywords

[No Author keywords available]

Indexed keywords

5 METHYLNAPHTHO[1,2 D]THIAZOL 2 AMINE; 5 METHYLNAPHTHO[2,1 D]OXAZOL 2 AMINE; BENZOTHIAZOLE; BENZOTHIAZOLE DERIVATIVE; INTERMEDIATE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL; POTASSIUM CHANNEL KV1.3; POTASSIUM CHANNEL KV11.1; POTASSIUM CHANNEL KV2.1; POTASSIUM CHANNEL KV3.1; SKA 111; SKA 121; SMALL CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL; SODIUM CHANNEL NAV1.2; SODIUM CHANNEL NAV1.4; SODIUM CHANNEL NAV1.5; SODIUM CHANNEL NAV1.7; UNCLASSIFIED DRUG; VOLTAGE GATED POTASSIUM CHANNEL; 5 METHYLNAPHTHO(2,1 D)OXAZOL 2 AMINE; 5-METHYLNAPHTHO(2,1-D)OXAZOL-2-AMINE; BRADYKININ; KCNN4 PROTEIN, HUMAN; NAPHTHO(1,2 D)THIAZOL 2 YLAMINE; NAPHTHO(1,2-D)THIAZOL-2-YLAMINE; OXAZOLE DERIVATIVE; VASODILATOR AGENT;

EID: 84906308946     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.114.093286     Document Type: Article
Times cited : (45)

References (51)
  • 2
    • 84866744757 scopus 로고    scopus 로고
    • +) channels: A novel target for medicinal chemistry efforts?
    • +) channels: a novel target for medicinal chemistry efforts? ChemMedChem 7:1741-1755.
    • (2012) ChemMedChem , vol.7 , pp. 1741-1755
    • Balut, C.M.1    Hamilton, K.L.2    Devor, D.C.3
  • 4
    • 66349089328 scopus 로고    scopus 로고
    • Genetic deficit of SK3 and IK1 channels disrupts the endothelium-derived hyperpolarizing factor vasodilator pathway and causes hypertension
    • Brähler S, Kaistha A, Schmidt VJ, Wölfle SE, Busch C, Kaistha BP, Kacik M, Hasenau AL, Grgic I, and Si H et al. (2009) Genetic deficit of SK3 and IK1 channels disrupts the endothelium-derived hyperpolarizing factor vasodilator pathway and causes hypertension. Circulation 119:2323-2332.
    • (2009) Circulation , vol.119 , pp. 2323-2332
    • Brähler, S.1    Kaistha, A.2    Schmidt, V.J.3    Wölfle, S.E.4    Busch, C.5    Kaistha, B.P.6    Kacik, M.7    Hasenau, A.L.8    Grgic, I.9    Si, H.10
  • 8
    • 77954812252 scopus 로고    scopus 로고
    • Calcium-activated potassium channels - A therapeutic target for modulating nitric oxide in cardiovascular disease?
    • Dalsgaard T, Kroigaard C, and Simonsen U (2010) Calcium-activated potassium channels - a therapeutic target for modulating nitric oxide in cardiovascular disease? Expert Opin Ther Targets 14:825-837.
    • (2010) Expert Opin Ther Targets , vol.14 , pp. 825-837
    • Dalsgaard, T.1    Kroigaard, C.2    Simonsen, U.3
  • 10
    • 0027213025 scopus 로고
    • Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenpus oocytes
    • Debono MW, Le Guern J, Canton T, Doble A, and Pradier L (1993) Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes. Eur J Pharmacol 235:283-289. (Pubitemid 23130445)
    • (1993) European Journal of Pharmacology , vol.235 , Issue.2-3 , pp. 283-289
    • Debono, M.-W.1    Le, G.J.2    Canton, T.3    Doble, A.4    Pradier, L.5
  • 13
    • 77955292086 scopus 로고    scopus 로고
    • Endothelium-derived hyperpolarising factors and associated pathways: A synopsis
    • Edwards G, Félétou M, and Weston AH (2010) Endothelium-derived hyperpolarising factors and associated pathways: a synopsis. Pflugers Arch 459:863 -879.
    • (2010) Pflugers Arch , vol.459 , pp. 863-879
    • Edwards, G.1    Félétou, M.2    Weston, A.H.3
  • 16
    • 84893123362 scopus 로고    scopus 로고
    • Aromatic-aromatic interactions between residues in KCa3.1 pore helix and S5 transmembrane segment control the channel gating process
    • Garneau L, Klein H, Lavoie MF, Brochiero E, Parent L, and Sauvé R (2014) Aromatic-aromatic interactions between residues in KCa3.1 pore helix and S5 transmembrane segment control the channel gating process. J Gen Physiol 143:289-307.
    • (2014) J Gen Physiol , vol.143 , pp. 289-307
    • Garneau, L.1    Klein, H.2    Lavoie, M.F.3    Brochiero, E.4    Parent, L.5    Sauvé, R.6
  • 18
    • 13844310156 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers
    • DOI 10.1016/j.bmc.2005.01.006
    • Göblyös A, Santiago SN, Pietra D, Mulder-Krieger T, von Frijtag Drabbe Künzel J, Brussee J, and Ijzerman AP (2005) Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers. Bioorg Med Chem 13:2079-2087. (Pubitemid 40261128)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.6 , pp. 2079-2087
    • Goblyos, A.1    Santiago, S.N.2    Pietra, D.3    Mulder-Krieger, T.4    Kunzel, J.V.F.D.5    Brussee, J.6    Ijzerman, A.P.7
  • 19
    • 70349895458 scopus 로고    scopus 로고
    • Endothelial Ca+-activated K+ channels in normal and impaired EDHF-dilator responses: Relevance to cardiovascular pathologies and drug discovery
    • Grgic I, Kaistha BP, Hoyer J, and Köhler R (2009) Endothelial Ca+-activated K+ channels in normal and impaired EDHF-dilator responses: relevance to cardiovascular pathologies and drug discovery. Br J Pharmacol 157:509-526.
    • (2009) Br J Pharmacol , vol.157 , pp. 509-526
    • Grgic, I.1    Kaistha, B.P.2    Hoyer, J.3    Köhler, R.4
  • 23
    • 84856068484 scopus 로고    scopus 로고
    • Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype
    • Hougaard C, Hammami S, Eriksen BL, Sørensen US, Jensen ML, Strøbæk D, and Christophersen P (2012) Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype. Mol Pharmacol 81:210-219.
    • (2012) Mol Pharmacol , vol.81 , pp. 210-219
    • Hougaard, C.1    Hammami, S.2    Eriksen, B.L.3    Sørensen, U.S.4    Jensen, M.L.5    Strøbæk, D.6    Christophersen, P.7
  • 25
    • 84890903984 scopus 로고    scopus 로고
    • Development of a QPatch automated electrophysiology assay for identifying KCa3.1 inhibitors and activators
    • Jenkins DP, Yu W, Brown BM, Løjkner LD, and Wulff H (2013) Development of a QPatch automated electrophysiology assay for identifying KCa3.1 inhibitors and activators. Assay Drug Dev Technol 11:551-560.
    • (2013) Assay Drug Dev Technol , vol.11 , pp. 551-560
    • Jenkins, D.P.1    Yu, W.2    Brown, B.M.3    Løjkner, L.D.4    Wulff, H.5
  • 28
    • 0142227938 scopus 로고    scopus 로고
    • Efficient Conversion of Substituted Aryl Thioureas to 2-Aminobenzothiazoles Using Benzyltrimethylammonium Tribromide
    • DOI 10.1021/jo0349431
    • Jordan AD, Luo C, and Reitz AB (2003) Efficient conversion of substituted aryl thioureas to 2-aminobenzothiazoles using benzyltrimethylammonium tribromide. J Org Chem 68:8693-8696. (Pubitemid 37329133)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.22 , pp. 8693-8696
    • Jordan, A.D.1    Luo, C.2    Reitz, A.B.3
  • 30
    • 33947714200 scopus 로고    scopus 로고
    • Structural determinants of the closed KCa3.1 channel pore in relation to channel gating: Results from a substituted cysteine accessibility analysis
    • DOI 10.1085/jgp.200609726
    • Klein H, Garneau L, Banderali U, Simoes M, Parent L, and Sauvé R (2007) Structural determinants of the closed KCa3.1 channel pore in relation to channel gating: results from a substituted cysteine accessibility analysis. J Gen Physiol 129:299-315. (Pubitemid 46506981)
    • (2007) Journal of General Physiology , vol.129 , Issue.4 , pp. 299-315
    • Klein, H.1    Garneau, L.2    Banderali, U.3    Simoes, M.4    Parent, L.5    Sauve, R.6
  • 32
    • 84906315551 scopus 로고    scopus 로고
    • Cardiovascular alterations in KCa3.1/KCa2.3-deficient mice and after acute treatment with KCa3.1/KCa2.3 activators
    • Feletou M, Vanhoutte PM (eds) Vaux-de-Cernay, France
    • Köhler R (2012) Cardiovascular alterations in KCa3.1/KCa2.3- deficient mice and after acute treatment with KCa3.1/KCa2.3 activators. EDHF 2012: 10th Anniversary Meeting June 27th-30th, 2012; Feletou M, Vanhoutte PM (eds) vol. 49, pp 1-54 Vaux-de-Cernay, France.
    • (2012) EDHF 2012: 10th Anniversary Meeting June 27th-30th, 2012 , vol.49 , pp. 1-54
    • Köhler, R.1
  • 33
    • 74949130493 scopus 로고    scopus 로고
    • Vascular KCa-channels as therapeutic targets in hypertension and restenosis disease
    • Köhler R, Kaistha BP, and Wulff H (2010) Vascular KCa-channels as therapeutic targets in hypertension and restenosis disease. Expert Opin Ther Targets 14:143-155.
    • (2010) Expert Opin Ther Targets , vol.14 , pp. 143-155
    • Köhler, R.1    Kaistha, B.P.2    Wulff, H.3
  • 34
    • 70349641039 scopus 로고    scopus 로고
    • EF hands at the N-lobe of calmodulin are required for both SK channel gating and stable SK-calmodulin interaction
    • Li W, Halling DB, Hall AW, and Aldrich RW (2009) EF hands at the N-lobe of calmodulin are required for both SK channel gating and stable SK-calmodulin interaction. J Gen Physiol 134:281-293.
    • (2009) J Gen Physiol , vol.134 , pp. 281-293
    • Li, W.1    Halling, D.B.2    Hall, A.W.3    Aldrich, R.W.4
  • 35
    • 64549097688 scopus 로고    scopus 로고
    • Endothelium-derived hyperpolarizing factor mediated relaxations in pig coronary arteries do not involve Gi/o proteins
    • Ng KF, Leung SW, Man RY, and Vanhoutte PM (2008) Endothelium-derived hyperpolarizing factor mediated relaxations in pig coronary arteries do not involve Gi/o proteins. Acta Pharmacol Sin 29:1419-1424.
    • (2008) Acta Pharmacol Sin , vol.29 , pp. 1419-1424
    • Ng, K.F.1    Leung, S.W.2    Man, R.Y.3    Vanhoutte, P.M.4
  • 37
    • 84883260008 scopus 로고    scopus 로고
    • Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient mice
    • Radtke J, Schmidt K, Wulff H, Köhler R, and de Wit C (2013) Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient mice. Br J Pharmacol 170:293-303.
    • (2013) Br J Pharmacol , vol.170 , pp. 293-303
    • Radtke, J.1    Schmidt, K.2    Wulff, H.3    Köhler, R.4    De Wit, C.5
  • 38
    • 0031603012 scopus 로고    scopus 로고
    • + channel
    • Rosa JC, Galanakis D, Ganellin CR, Dunn PM, and Jenkinson DH (1998) Bis-quinolinium cyclophanes: 6,10-diaza-3(1,3),8(1,4)-dibenzena-1,5(1,4)- diquinolinacyclodecaphane (UCL 1684), the first nanomolar, non-peptidic blocker of the apamin-sensitive Ca(2+)-activated K+ channel. J Med Chem 41:2-5. (Pubitemid 128719272)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.1 , pp. 2-5
    • Rosa, J.C.1    Galanakis, D.2    Ganellin, C.R.3    Dunn, P.M.4    Jenkinson, D.H.5
  • 39
    • 59449098672 scopus 로고    scopus 로고
    • Naphtho[1,2-d]thiazol-2-ylamine (SKA-31), a new activator of KCa2 and KCa3.1 potassium channels, potentiates the endothelium-derived hyperpolarizing factor response and lowers blood pressure
    • Sankaranarayanan A, Raman G, Busch C, Schultz T, Zimin PI, Hoyer J, Köhler R, and Wulff H (2009) Naphtho[1,2-d]thiazol-2-ylamine (SKA-31), a new activator of KCa2 and KCa3.1 potassium channels, potentiates the endothelium-derived hyperpolarizing factor response and lowers blood pressure. Mol Pharmacol 75:281-295.
    • (2009) Mol Pharmacol , vol.75 , pp. 281-295
    • Sankaranarayanan, A.1    Raman, G.2    Busch, C.3    Schultz, T.4    Zimin, P.I.5    Hoyer, J.6    Köhler, R.7    Wulff, H.8
  • 40
    • 27544454783 scopus 로고    scopus 로고
    • Design of PAP-1, a selective small molecule Kv1.3 blocker, for the suppression of effector memory t cells in autoimmune diseases
    • DOI 10.1124/mol.105.015669
    • Schmitz A, Sankaranarayanan A, Azam P, Schmidt-Lassen K, Homerick D, Hänsel W, and Wulff H (2005) Design of PAP-1, a selective small molecule Kv1.3 blocker, for the suppression of effector memory T cells in autoimmune diseases. Mol Pharmacol 68:1254-1270. (Pubitemid 41539982)
    • (2005) Molecular Pharmacology , vol.68 , Issue.5 , pp. 1254-1270
    • Schmitz, A.1    Sankaranarayanan, A.2    Azam, P.3    Schmidt-Lassen, K.4    Homerick, D.5    Hansel, W.6    Wulff, H.7
  • 41
    • 0015882117 scopus 로고
    • [2-Aminooxazoles and 2-iminooxazolines. 1: Reaction of racemic alpha-methylaminopropiophenone using cyanobromide]
    • Schuart J and Müller HK (1973) [2-Aminooxazoles and 2-iminooxazolines. 1: reaction of racemic alpha-methylaminopropiophenone using cyanobromide]. Pharmazie 28:438-439.
    • (1973) Pharmazie , vol.28 , pp. 438-439
    • Schuart, J.1    Müller, H.K.2
  • 42
    • 37549039510 scopus 로고    scopus 로고
    • A short history of SHELX
    • Sheldrick GM (2008) A short history of SHELX. Acta Crystallogr A 64:112-122.
    • (2008) Acta Crystallogr A , vol.64 , pp. 112-122
    • Sheldrick, G.M.1
  • 43
    • 0035146762 scopus 로고    scopus 로고
    • Benzimidazolone activators of chloride secretion: Potentialtherapeutics for cystic fibrosis and chronic obstructive pulmonarydisease
    • Singh S, Syme CA, Singh AK, Devor DC, and Bridges RJ (2001) Benzimidazolone activators of chloride secretion: potential therapeutics for cystic fibrosis and chronic obstructive pulmonary disease. J Pharmacol Exp Ther 296:600-611. (Pubitemid 32112491)
    • (2001) Journal of Pharmacology and Experimental Therapeutics , vol.296 , Issue.2 , pp. 600-611
    • Singh, S.1    Syme, C.A.2    Singh, A.K.3    Devor, D.C.4    Bridges, R.J.5
  • 45
    • 29844439979 scopus 로고    scopus 로고
    • International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels
    • DOI 10.1124/pr.57.4.9
    • Wei AD, Gutman GA, Aldrich R, Chandy KG, Grissmer S, and Wulff H (2005) International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels. Pharmacol Rev 57:463-472. (Pubitemid 43036436)
    • (2005) Pharmacological Reviews , vol.57 , Issue.4 , pp. 463-472
    • Wei, A.D.1    Gutman, G.A.2    Aldrich, R.3    Chandy, K.G.4    Grissmer, S.5    Wulff, H.6
  • 46
    • 84873414518 scopus 로고    scopus 로고
    • Endothelial small-conductance and intermediate-conductance KCa channels: An update on their pharmacology and usefulness as cardiovascular targets
    • Wulff H and Köhler R (2013) Endothelial small-conductance and intermediate-conductance KCa channels: an update on their pharmacology and usefulness as cardiovascular targets. J Cardiovasc Pharmacol 61:102-112.
    • (2013) J Cardiovasc Pharmacol , vol.61 , pp. 102-112
    • Wulff, H.1    Köhler, R.2
  • 48
    • 44849093511 scopus 로고    scopus 로고
    • + channel modulators for the treatment of neurological disorders and autoimmune diseases
    • + channel modulators for the treatment of neurological disorders and autoimmune diseases. Chem Rev 108:1744-1773.
    • (2008) Chem Rev , vol.108 , pp. 1744-1773
    • Wulff, H.1    Zhorov, B.S.2


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