메뉴 건너뛰기




Volumn 314, Issue 2, 2005, Pages 891-905

Phenoxybenzamine and benextramine, but not 4-diphenylacetoxy-N-[2- chloroethyl]piperidine hydrochloride, display irreversible noncompetitive antagonism at G protein-coupled receptors

Author keywords

[No Author keywords available]

Indexed keywords

1 (2 CHLOROETHYL) 4 DIPHENYLACETOXYPIPERIDINE; ALPHA 2A ADRENERGIC RECEPTOR; BENEXTRAMINE; G PROTEIN COUPLED RECEPTOR; GUANOSINE 5' O (3 THIOTRIPHOSPHATE); MUSCARINIC RECEPTOR; PHENOXYBENZAMINE; SEROTONIN 2A RECEPTOR; SULFUR 35;

EID: 22944471442     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: 10.1124/jpet.105.083568     Document Type: Article
Times cited : (8)

References (69)
  • 1
    • 0027456415 scopus 로고
    • Receptor reserve masks partial agonist activity of drugs in a cloned rat 5-hydroxytryptamine1B receptor expression system
    • Adham N, Ellerbrock B, Hartig P, Weinshank RL, and Branchek T (1993) Receptor reserve masks partial agonist activity of drugs in a cloned rat 5-hydroxytryptamine1B receptor expression system. Mol Pharmacol 43:427-433.
    • (1993) Mol Pharmacol , vol.43 , pp. 427-433
    • Adham, N.1    Ellerbrock, B.2    Hartig, P.3    Weinshank, R.L.4    Branchek, T.5
  • 2
    • 0027530780 scopus 로고
    • 2-autoreceptors: Agonist dissociation constants and recovery after irreversible activation
    • 2- autoreceptors: agonist dissociation constants and recovery after irreversible activation. Br J Pharmacol 108:370-375.
    • (1993) Br J Pharmacol , vol.108 , pp. 370-375
    • Agneter, E.1    Drobny, H.2    Singer, E.A.3
  • 3
    • 0029060175 scopus 로고
    • Differential inhibition in the human vas deferens by phenoxybenzamine: A possible mechanism for its contraceptive action
    • Amobi NI and Smith IC (1995) Differential inhibition in the human vas deferens by phenoxybenzamine: a possible mechanism for its contraceptive action. J Reprod Fertil 103:215-221.
    • (1995) J Reprod Fertil , vol.103 , pp. 215-221
    • Amobi, N.I.1    Smith, I.C.2
  • 4
    • 0032586855 scopus 로고    scopus 로고
    • 1A receptor agonists of restraint stress- and yohimbine-induced release of cholecystokinin in the frontal cortex of the freely moving rat
    • 1A receptor agonists of restraint stress- and yohimbine-induced release of cholecystokinin in the frontal cortex of the freely moving rat. Neuropharmacology 38:525-532.
    • (1999) Neuropharmacology , vol.38 , pp. 525-532
    • Becker, C.1    Hamon, M.2    Benoliel, J.-J.3
  • 6
    • 0020075511 scopus 로고
    • Inhibition of adrenaline-induced platelet aggregation by the -adrenoceptor blocking drug benextramine
    • Belleau B, Benfey BG, Melchiorre C, and Montambault M (1982b) Inhibition of adrenaline-induced platelet aggregation by the -adrenoceptor blocking drug benextramine. Br J Pharmacol 76:253-257.
    • (1982) Br J Pharmacol , vol.76 , pp. 253-257
    • Belleau, B.1    Benfey, B.G.2    Melchiorre, C.3    Montambault, M.4
  • 7
    • 0019274478 scopus 로고
    • Irreversible alpha adrenoceptor blocking effects and reversible muscarinic blocking and nicotinic blocking effects of tetramine disulfides on the heart
    • Benfey BG, Belleau B, Brasili L, Giannella M, and Melchiorre C (1980) Irreversible alpha adrenoceptor blocking effects and reversible muscarinic blocking and nicotinic blocking effects of tetramine disulfides on the heart. Can J Physiol Pharmacol 58:1477-1483.
    • (1980) Can J Physiol Pharmacol , vol.58 , pp. 1477-1483
    • Benfey, B.G.1    Belleau, B.2    Brasili, L.3    Giannella, M.4    Melchiorre, C.5
  • 8
    • 0027397544 scopus 로고
    • Inositol trisphosphate and calcium signalling
    • Berridge MJ (1993) Inositol trisphosphate and calcium signalling. Nature (Lond) 361:315-325.
    • (1993) Nature (Lond) , vol.361 , pp. 315-325
    • Berridge, M.J.1
  • 9
    • 0001531574 scopus 로고
    • Use of U-73122 as an inhibitor of phospholipase C-dependent processes
    • Bleasdale JE and Fisher SK (1993) Use of U-73122 as an inhibitor of phospholipase C-dependent processes. Neuroprotocols 3:125-133.
    • (1993) Neuroprotocols , vol.3 , pp. 125-133
    • Bleasdale, J.E.1    Fisher, S.K.2
  • 10
    • 0028245619 scopus 로고
    • Molecular biology of 5-HT receptors
    • Boess FG and Martin IL (1994) Molecular biology of 5-HT receptors. Neuropharmacology 33:275-317.
    • (1994) Neuropharmacology , vol.33 , pp. 275-317
    • Boess, F.G.1    Martin, I.L.2
  • 12
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254.
    • (1976) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 14
    • 0019296727 scopus 로고
    • Reactivation by cysteamine of vascular alpha adrenoceptors blocked by the tetramine disulfide benextramine and interaction of benextramine with phenoxybenzamine
    • Brasili L, Melchiorre C, Belleau B, and Benfey BG (1980) Reactivation by cysteamine of vascular alpha adrenoceptors blocked by the tetramine disulfide benextramine and interaction of benextramine with phenoxybenzamine. Can J Physiol Pharmacol 58:1490-1493.
    • (1980) Can J Physiol Pharmacol , vol.58 , pp. 1490-1493
    • Brasili, L.1    Melchiorre, C.2    Belleau, B.3    Benfey, B.G.4
  • 17
    • 0028168350 scopus 로고
    • 2A-adrenergic receptor to multiple G-proteins. A simple approach for estimating receptor-G-protein coupling efficiency in a transient expression system
    • 2A-adrenergic receptor to multiple G-proteins. A simple approach for estimating receptor-G-protein coupling efficiency in a transient expression system. J Biol Chem 269:5730-5734.
    • (1994) J Biol Chem , vol.269 , pp. 5730-5734
    • Chabre, O.1    Conklin, B.R.2    Brandon, S.3    Bourne, H.R.4    Limbird, L.E.5
  • 18
    • 0014218903 scopus 로고
    • Pheochromocytoma. Treatment with alpha- and beta-adrenergic blocking drugs
    • Crago RM, Eckholdt JW, and Wismell JG (1967) Pheochromocytoma. Treatment with alpha- and beta-adrenergic blocking drugs. J Am Med Assoc 202:870-874.
    • (1967) J Am Med Assoc , vol.202 , pp. 870-874
    • Crago, R.M.1    Eckholdt, J.W.2    Wismell, J.G.3
  • 19
    • 0026741825 scopus 로고
    • Simultaneous coupling of alpha 2-adrenergic receptors to two G-proteins with opposing effects. Subtype-selective coupling of alpha 2C10, alpha 2C4 and alpha 2C2 adrenergic receptors to Gi and Gs
    • Eason MG, Kurose H, Holt BD, Raymond JR, and Liggett SB (1992) Simultaneous coupling of alpha 2-adrenergic receptors to two G-proteins with opposing effects. Subtype-selective coupling of alpha 2C10, alpha 2C4 and alpha 2C2 adrenergic receptors to Gi and Gs. J Biol Chem 267:15795-15801.
    • (1992) J Biol Chem , vol.267 , pp. 15795-15801
    • Eason, M.G.1    Kurose, H.2    Holt, B.D.3    Raymond, J.R.4    Liggett, S.B.5
  • 20
    • 0028670460 scopus 로고
    • Selective inactivation of muscarinic receptor subtypes
    • Eglen RM, Reddy H, and Watson N (1994) Selective inactivation of muscarinic receptor subtypes. Int J Biochem 26:1357-1368.
    • (1994) Int J Biochem , vol.26 , pp. 1357-1368
    • Eglen, R.M.1    Reddy, H.2    Watson, N.3
  • 21
    • 0032571228 scopus 로고    scopus 로고
    • The use of irreversible ligands to inactivate receptor subtypes: 4-DAMP mustard and muscarinic receptors in smooth muscle
    • Ehlert FJ and Griffin MT (1998) The use of irreversible ligands to inactivate receptor subtypes: 4-DAMP mustard and muscarinic receptors in smooth muscle. Life Sci 62:1659-1664.
    • (1998) Life Sci , vol.62 , pp. 1659-1664
    • Ehlert, F.J.1    Griffin, M.T.2
  • 22
    • 0035903167 scopus 로고    scopus 로고
    • Phenoxybenzamine binding reveals the helical orientation of the third transmembrane domain of adrenergic receptors
    • Frang H, Cockroft V, Karskela T, Scheinin M, and Marjamäki A (2001) Phenoxybenzamine binding reveals the helical orientation of the third transmembrane domain of adrenergic receptors. J Biol Chem 276:31279-31284.
    • (2001) J Biol Chem , vol.276 , pp. 31279-31284
    • Frang, H.1    Cockroft, V.2    Karskela, T.3    Scheinin, M.4    Marjamäki, A.5
  • 23
    • 0002355204 scopus 로고
    • The use of β-haloalkylamines in the differentiation of receptors and in the determination of dissociation constants of receptor-agonist complexes
    • (Harper NJ and Simmonds AB eds), Academic Press, New York
    • Furchgott RF (1966) The use of β-haloalkylamines in the differentiation of receptors and in the determination of dissociation constants of receptor-agonist complexes, in Advances in Drug Research (Harper NJ and Simmonds AB eds), vol 3, pp 21-55, Academic Press, New York.
    • (1966) Advances in Drug Research , vol.3 , pp. 21-55
    • Furchgott, R.F.1
  • 26
    • 0028956203 scopus 로고
    • Synthesis and α-adrenoceptor blocking properties of phenoxybenzamine-related (2-chloroethyl)-(2,3-dihidrobenzo[1,4]dioxin-2- ylmethyl)-(2-phenoxyethyl) amines
    • Giardinà D, Crucianelli M, Marucci G, Paparelli F, and Melchiorre C (1995) Synthesis and α-adrenoceptor blocking properties of phenoxybenzamine-related (2-chloroethyl)-(2,3-dihidrobenzo[1,4]dioxin-2- ylmethyl)-(2-phenoxyethyl) amines. Bioorg Med Chem 3:85-94.
    • (1995) Bioorg Med Chem , vol.3 , pp. 85-94
    • Giardinà, D.1    Crucianelli, M.2    Marucci, G.3    Paparelli, F.4    Melchiorre, C.5
  • 28
    • 0026542256 scopus 로고
    • Expression and purification of functional G protein α subunits using a baculovirus expression system
    • Graber SG, Figler RA, and Garrison JC (1992) Expression and purification of functional G protein α subunits using a baculovirus expression system. J Biol Chem 267:1271-1278.
    • (1992) J Biol Chem , vol.267 , pp. 1271-1278
    • Graber, S.G.1    Figler, R.A.2    Garrison, J.C.3
  • 29
    • 0025298667 scopus 로고
    • Affinities of full agonists for cardiac β-adrenoceptors calculated by use of in vitro desensitisation
    • Herepath ML and Broadley KJ (1990) Affinities of full agonists for cardiac β-adrenoceptors calculated by use of in vitro desensitisation. Naunyn-Schmiedeberg's Arch Pharmacol 341:525-533.
    • (1990) Naunyn-Schmiedeberg's Arch Pharmacol , vol.341 , pp. 525-533
    • Herepath, M.L.1    Broadley, K.J.2
  • 30
    • 0021956263 scopus 로고
    • In vitro characterization of the α-adrenoceptors in human prostate
    • Hieble JP, Caine M, and Zalaznik E (1985) In vitro characterization of the α-adrenoceptors in human prostate. Eur J Pharmacol 107:111-117.
    • (1985) Eur J Pharmacol , vol.107 , pp. 111-117
    • Hieble, J.P.1    Caine, M.2    Zalaznik, E.3
  • 31
    • 0035032869 scopus 로고    scopus 로고
    • Pharmacological properties of (2R)-N-[1-(6-aminopyridin-2-ylmethyl) piperidin-4-yl]-2-[(1R)-3,3-difluorocyclopentyl]-2-hydroxy-2-phenylacetamide: A novel muscarinic antagonist with M2-sparing antagonistic activity
    • Hirose H, Aoki I, Kimura T, Fujikawa T, Numazawa T, Sasaki K, Sato A, Hasegawa T, Nishikibe M, Mitsuya M, et al. (2001) Pharmacological properties of (2R)-N-[1-(6-aminopyridin-2-ylmethyl)piperidin-4-yl]-2-[(1R)-3, 3-difluorocyclopentyl]-2-hydroxy-2-phenylacetamide: a novel muscarinic antagonist with M2-sparing antagonistic activity. J Pharmacol Exp Ther 297:790-797.
    • (2001) J Pharmacol Exp Ther , vol.297 , pp. 790-797
    • Hirose, H.1    Aoki, I.2    Kimura, T.3    Fujikawa, T.4    Numazawa, T.5    Sasaki, K.6    Sato, A.7    Hasegawa, T.8    Nishikibe, M.9    Mitsuya, M.10
  • 32
    • 0002014752 scopus 로고    scopus 로고
    • Classical approaches to the study of drug-receptor interactions
    • (Foreman JC and Johansen T eds) CRC Press, Boca Raton
    • Jenkinson DH (2003) Classical approaches to the study of drug-receptor interactions, in Textbook of Receptor Pharmacology (Foreman JC and Johansen T eds) pp 3-78, CRC Press, Boca Raton.
    • (2003) Textbook of Receptor Pharmacology , pp. 3-78
    • Jenkinson, D.H.1
  • 34
    • 0034079628 scopus 로고    scopus 로고
    • 1A receptors: Effects of EEDQ on the ability of agonists to produce lower-lip retraction in rats
    • 1A receptors: effects of EEDQ on the ability of agonists to produce lower-lip retraction in rats. Psychopharmacology (Berl) 149:377-387.
    • (2000) Psychopharmacology (Berl) , vol.149 , pp. 377-387
    • Koek, W.1    Assie, M.B.2    Zernig, G.3    France, C.P.4
  • 35
    • 0026970161 scopus 로고
    • Muscarinic receptor subtypes in human neuroblastoma cell lines SH-SY5Y and IMR-32 as determined by receptor binding, Ca++ mobilization and northern blotting
    • Kukkonen J, Ojala P, Näsman J, Hämäläinen H, Heikkilä J, and Åkerman KE (1992) Muscarinic receptor subtypes in human neuroblastoma cell lines SH-SY5Y and IMR-32 as determined by receptor binding, Ca++ mobilization and northern blotting. J Pharmacol Exp Ther 263:1487-1493.
    • (1992) J Pharmacol Exp Ther , vol.263 , pp. 1487-1493
    • Kukkonen, J.1    Ojala, P.2    Näsman, J.3    Hämäläinen, H.4    Heikkilä, J.5    Åkerman, K.E.6
  • 36
    • 0024391759 scopus 로고
    • Muscarinic receptor binding characteristics of a human neuroblastoma SK-N-SH and its clones SH-SY5Y and SH-EP1
    • Lambert DG, Ghataorre AS, and Nahorski SR (1989) Muscarinic receptor binding characteristics of a human neuroblastoma SK-N-SH and its clones SH-SY5Y and SH-EP1. Eur J Pharmacol 165:71-77.
    • (1989) Eur J Pharmacol , vol.165 , pp. 71-77
    • Lambert, D.G.1    Ghataorre, A.S.2    Nahorski, S.R.3
  • 37
    • 0021359216 scopus 로고
    • Reversible inhibition of neuronal uptake by benextramine, an irreversible presynaptic α-adrenoceptor antagonist
    • Lew MJ and Angus JA (1984) Reversible inhibition of neuronal uptake by benextramine, an irreversible presynaptic α-adrenoceptor antagonist. Eur J Pharmacol 98:27-34.
    • (1984) Eur J Pharmacol , vol.98 , pp. 27-34
    • Lew, M.J.1    Angus, J.A.2
  • 38
    • 0023830043 scopus 로고
    • 2- adrenergic receptors in human erythroleukemia (HEL) cells. Studies with the irreversible antagonist benextramine
    • 2-adrenergic receptors in human erythroleukemia (HEL) cells. Studies with the irreversible antagonist benextramine. Mol Pharmacol 33:51-57.
    • (1988) Mol Pharmacol , vol.33 , pp. 51-57
    • McKernan, R.M.1    Strickland, W.R.2    Insel, P.A.3
  • 39
    • 0001460864 scopus 로고
    • Tetramine disulfides: A new tool in α-adrenergic pharmacology
    • Melchiorre C (1981) Tetramine disulfides: a new tool in α-adrenergic pharmacology. Trends Pharmacol Sci 2:209-211.
    • (1981) Trends Pharmacol Sci , vol.2 , pp. 209-211
    • Melchiorre, C.1
  • 41
    • 0021074131 scopus 로고
    • The irreversible α-blocker benextramine interacts with two different thiol groups
    • Melchiorre C and Gallucci P (1983) The irreversible α-blocker benextramine interacts with two different thiol groups. Farm Ed Sci 38:950-956.
    • (1983) Farm Ed Sci , vol.38 , pp. 950-956
    • Melchiorre, C.1    Gallucci, P.2
  • 42
    • 0028029617 scopus 로고
    • Binding profile of benextramine at neuropeptide Y receptor subtypes in rat brain areas
    • Melchiorre C, Romualdi P, Bolognesi ML, Donatini A, and Ferri S (1994) Binding profile of benextramine at neuropeptide Y receptor subtypes in rat brain areas. Eur J Pharmacol 265:93-98.
    • (1994) Eur J Pharmacol , vol.265 , pp. 93-98
    • Melchiorre, C.1    Romualdi, P.2    Bolognesi, M.L.3    Donatini, A.4    Ferri, S.5
  • 44
    • 0345490945 scopus 로고    scopus 로고
    • International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology
    • Neubig RR, Spedding M, Kenakin T, and Christopoulos A (2003) International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology. Pharmacol Rev 55:597-606.
    • (2003) Pharmacol Rev , vol.55 , pp. 597-606
    • Neubig, R.R.1    Spedding, M.2    Kenakin, T.3    Christopoulos, A.4
  • 45
    • 0026331434 scopus 로고
    • Muscarinic stimulation of adenylate cyclase activity of rat olfactory bulb. I. Analysis of agonist sensitivity
    • Olianas MC and Onali P (1991) Muscarinic stimulation of adenylate cyclase activity of rat olfactory bulb. I. Analysis of agonist sensitivity. J Pharmacol Exp Ther 259:673-679.
    • (1991) J Pharmacol Exp Ther , vol.259 , pp. 673-679
    • Olianas, M.C.1    Onali, P.2
  • 46
    • 0023697090 scopus 로고
    • Alkylation of alpha-1 receptors with a chemically reactive analog of prazosin reveals low affinity sites for norepinephrine in rabbit aorta
    • Piascik MT, Kusiak JW, Pitha J, Butler BT, Le HT, and Babich M (1988) Alkylation of alpha-1 receptors with a chemically reactive analog of prazosin reveals low affinity sites for norepinephrine in rabbit aorta. J Pharmacol Exp Ther 246:1001-1011.
    • (1988) J Pharmacol Exp Ther , vol.246 , pp. 1001-1011
    • Piascik, M.T.1    Kusiak, J.W.2    Pitha, J.3    Butler, B.T.4    Le, H.T.5    Babich, M.6
  • 47
    • 0035016227 scopus 로고    scopus 로고
    • Pharmacological and functional characterization of muscarinic receptor subtypes in developing oligodendrocytes
    • Ragheb F, Molina-Holgado E, Cui Q-L, Khorchid A, Liu H-N, Larocca JN, and Almazan G (2001) Pharmacological and functional characterization of muscarinic receptor subtypes in developing oligodendrocytes. J Neurochem 77:1396-1406.
    • (2001) J Neurochem , vol.77 , pp. 1396-1406
    • Ragheb, F.1    Molina-Holgado, E.2    Cui, Q.-L.3    Khorchid, A.4    Liu, H.-N.5    Larocca, J.N.6    Almazan, G.7
  • 49
    • 0032999135 scopus 로고    scopus 로고
    • Adrenoceptor pharmacology: Urogenital applications
    • Ruffolo RR and Hieble JP (1999) Adrenoceptor pharmacology: urogenital applications. Eur Urol 36 (Suppl 1):17-22.
    • (1999) Eur Urol , vol.36 , Issue.1 SUPPL. , pp. 17-22
    • Ruffolo, R.R.1    Hieble, J.P.2
  • 50
    • 0016374975 scopus 로고
    • A highly sensitive adenylate cyclase assay
    • Salomon Y, Londos C, and Rodbell M (1974) A highly sensitive adenylate cyclase assay. Anal Biochem 58:541-548.
    • (1974) Anal Biochem , vol.58 , pp. 541-548
    • Salomon, Y.1    Londos, C.2    Rodbell, M.3
  • 52
    • 0030061672 scopus 로고    scopus 로고
    • Muscarinic receptor sequestration in SH-SY5Y neuroblastoma cells is inhibited when clathrin distribution is perturbed
    • Slowiejko DM, McEwen EL, Ernst SA, and Fisher SK (1996) Muscarinic receptor sequestration in SH-SY5Y neuroblastoma cells is inhibited when clathrin distribution is perturbed. J Neurochem 66:186-196.
    • (1996) J Neurochem , vol.66 , pp. 186-196
    • Slowiejko, D.M.1    McEwen, E.L.2    Ernst, S.A.3    Fisher, S.K.4
  • 55
    • 0021748090 scopus 로고
    • Isolation of two proteins with high affinity for guanine nucleotides from membranes of bovine brain
    • Sternweis PC and Robishaw JD (1984) Isolation of two proteins with high affinity for guanine nucleotides from membranes of bovine brain. J Biol Chem 259:13806-13813.
    • (1984) J Biol Chem , vol.259 , pp. 13806-13813
    • Sternweis, P.C.1    Robishaw, J.D.2
  • 57
    • 0027090012 scopus 로고
    • Conversion of N-(2-chloroethyl)-4-piperidinyl diphenylacetate (4-DAMP mustard) to an aziridinium ion and its interaction with muscarinic receptors in various tissues
    • Thomas EA, Hsu HH, Griffin MT, Hunter AL, Luong T, and Ehlert FJ (1992) Conversion of N-(2-chloroethyl)-4-piperidinyl diphenylacetate (4-DAMP mustard) to an aziridinium ion and its interaction with muscarinic receptors in various tissues. Mol Pharmacol 41:718-726.
    • (1992) Mol Pharmacol , vol.41 , pp. 718-726
    • Thomas, E.A.1    Hsu, H.H.2    Griffin, M.T.3    Hunter, A.L.4    Luong, T.5    Ehlert, F.J.6
  • 58
    • 0029995339 scopus 로고    scopus 로고
    • 2D-adrenergic receptor regulated G protein activation in PC12 cell membranes
    • 2D-adrenergic receptor regulated G protein activation in PC12 cell membranes. Pharmacology 52:252-262.
    • (1996) Pharmacology , vol.52 , pp. 252-262
    • Tian, W.C.1    Duzic, E.2    Deth, R.C.3
  • 61
    • 0030706126 scopus 로고    scopus 로고
    • On the reliability of affinity and efficacy estimates obtained by direct operational model fitting of agonist concentrationeffect curves following irreversible receptor inactivation
    • Van der Graaf PH and Danhof M (1997) On the reliability of affinity and efficacy estimates obtained by direct operational model fitting of agonist concentrationeffect curves following irreversible receptor inactivation. J Pharmacol Toxicol Methods 38:81-85.
    • (1997) J Pharmacol Toxicol Methods , vol.38 , pp. 81-85
    • Van Der Graaf, P.H.1    Danhof, M.2
  • 62
    • 0032737404 scopus 로고    scopus 로고
    • Analysis of receptor inactivation experiments with the operational model of agonism yields correlated estimates of agonist affinity and efficacy
    • Van der Graaf PH and Stam WB (1999) Analysis of receptor inactivation experiments with the operational model of agonism yields correlated estimates of agonist affinity and efficacy. J Pharmacol Toxicol Methods 41:117-125.
    • (1999) J Pharmacol Toxicol Methods , vol.41 , pp. 117-125
    • Van Der Graaf, P.H.1    Stam, W.B.2
  • 63
    • 0029935258 scopus 로고    scopus 로고
    • Benextramine acts as an irreversible noncompetitive antagonist of U46619-mediated contraction of the rat small mesenteric artery
    • Van der Graaf PH, Stam WB, and Saxena PR (1996) Benextramine acts as an irreversible noncompetitive antagonist of U46619-mediated contraction of the rat small mesenteric artery. Eur J Pharmacol 300:211-214.
    • (1996) Eur J Pharmacol , vol.300 , pp. 211-214
    • Van Der Graaf, P.H.1    Stam, W.B.2    Saxena, P.R.3
  • 64
    • 0343077527 scopus 로고
    • Kinetics of drug-receptor interaction
    • (Van Rossum JM ed) Springer-Verlag, Berlin
    • Van Ginneken CAM (1977) Kinetics of drug-receptor interaction, in Kinetics of Drug Action (Van Rossum JM ed) pp 357-411, Springer-Verlag, Berlin.
    • (1977) Kinetics of Drug Action , pp. 357-411
    • Van Ginneken, C.A.M.1
  • 66
    • 0028671807 scopus 로고
    • i assays in transfected cells
    • i assays in transfected cells. Methods Enzymol 238:81-94.
    • (1994) Methods Enzymol , vol.238 , pp. 81-94
    • Wong, Y.H.1
  • 67
    • 0032819108 scopus 로고    scopus 로고
    • Influence of G protein type on agonist efficacy
    • Yang Q and Lanier SM (1999) Influence of G protein type on agonist efficacy. Mol Pharmacol 56:651-656.
    • (1999) Mol Pharmacol , vol.56 , pp. 651-656
    • Yang, Q.1    Lanier, S.M.2
  • 68
    • 0027300816 scopus 로고
    • The competitive and noncompetitive antagonism of receptor-mediated drug actions in the presence of spare receptors
    • Zhu BT (1993) The competitive and noncompetitive antagonism of receptor-mediated drug actions in the presence of spare receptors. J Pharmacol Toxicol Methods 29:85-91.
    • (1993) J Pharmacol Toxicol Methods , vol.29 , pp. 85-91
    • Zhu, B.T.1
  • 69
    • 0030842275 scopus 로고    scopus 로고
    • Potentiation and inhibition of neuronal nicotinic receptors by atropine: Competitive and noncompetitive effects
    • Zwart R and Vijverberg HP (1997) Potentiation and inhibition of neuronal nicotinic receptors by atropine: competitive and noncompetitive effects. Mol Pharmacol 52:886-895.
    • (1997) Mol Pharmacol , vol.52 , pp. 886-895
    • Zwart, R.1    Vijverberg, H.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.