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Volumn 59, Issue 8, 2000, Pages 927-935

Reversible and syntopic interaction between angiotensin receptor antagonists on Chinese hamster ovary cells expressing human angiotensin II type 1 receptors

Author keywords

AT1 antagonists; Candesartan; CHO cells; EXP3174; Inositol phosphate; Insurmountable; Irbesartan; Losartan; Surmountable

Indexed keywords

2 BUTYL 4 CHLORO 1 [[2' (1H TETRAZOL 5 YL) 4 BIPHENYLYL]METHYL] 5 IMIDAZOLECARBOXYLIC ACID; ANGIOTENSIN 1 RECEPTOR; ANGIOTENSIN RECEPTOR ANTAGONIST; CANDESARTAN; IRBESARTAN; LOSARTAN;

EID: 0033969912     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-2952(99)00403-7     Document Type: Article
Times cited : (46)

References (33)
  • 1
    • 0000922757 scopus 로고
    • The renin-angiotensin system
    • Vallotton M.B. The renin-angiotensin system. Trends Pharmacol Sci. 8:1987;69-74.
    • (1987) Trends Pharmacol Sci , vol.8 , pp. 69-74
    • Vallotton, M.B.1
  • 2
    • 0000691888 scopus 로고    scopus 로고
    • Angiotensin antagonists
    • P. Leff. New York: Marcel Dekker
    • Robertson M.J. Angiotensin antagonists. Leff P. Receptor-Based Drug Design. 1998;207-229 Marcel Dekker, New York.
    • (1998) Receptor-Based Drug Design , pp. 207-229
    • Robertson, M.J.1
  • 9
    • 0026510753 scopus 로고
    • Evidence that the apparent complexity of receptor antagonism by angiotensin II analogues is due to a reversible and synoptic action
    • Liu Y.J., Shankley N.P., Welsh N.J., Black J.W. Evidence that the apparent complexity of receptor antagonism by angiotensin II analogues is due to a reversible and synoptic action. Br J Pharmacol. 106:1992;233-241.
    • (1992) Br J Pharmacol , vol.106 , pp. 233-241
    • Liu, Y.J.1    Shankley, N.P.2    Welsh, N.J.3    Black, J.W.4
  • 14
    • 0024603659 scopus 로고
    • Studies on inhibition of angiotensin II receptors in rabbit adrenal and aorta
    • Pendleton R.G., Gessner G., Horner E. Studies on inhibition of angiotensin II receptors in rabbit adrenal and aorta. J Pharmacol Exp Ther. 248:1989;637-643.
    • (1989) J Pharmacol Exp Ther , vol.248 , pp. 637-643
    • Pendleton, R.G.1    Gessner, G.2    Horner, E.3
  • 17
    • 0027218706 scopus 로고
    • Pharmacological characterization of the novel nonpeptide angiotensin II receptor antagonist, BIBR 277
    • Wienen W., Hauel N., Van Meel J.C., Narr B., Ries U., Entzeroth M. Pharmacological characterization of the novel nonpeptide angiotensin II receptor antagonist, BIBR 277. Br J Pharmacol. 110:1993;245-252.
    • (1993) Br J Pharmacol , vol.110 , pp. 245-252
    • Wienen, W.1    Hauel, N.2    Van Meel, J.C.3    Narr, B.4    Ries, U.5    Entzeroth, M.6
  • 18
    • 0028800752 scopus 로고
    • Elucidation of the insurmountable nature of an angiotensin receptor antagonist, SC-54629
    • Olins G.M., Chen S.T., McMahon E.G., Palomo M.A., Reitz D.B. Elucidation of the insurmountable nature of an angiotensin receptor antagonist, SC-54629. Mol Pharmacol. 47:1994;115-120.
    • (1994) Mol Pharmacol , vol.47 , pp. 115-120
    • Olins, G.M.1    Chen, S.T.2    McMahon, E.G.3    Palomo, M.A.4    Reitz, D.B.5
  • 22
    • 0027431141 scopus 로고
    • Pharmacological profile of a highly potent and long-acting angiotensin II receptor antagonist, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole- 7-carboxylic acid (CV-11974), and its prodrug, (±)-1-(cyclohexyloxycarbonyloxy)-ethyl-2-ethoxy-1-[ [ 2′-(1H-tetrazol-5-yl)biphenyl-4-yl ] methyl ]-1H-benzimidazole-7-carboxylate (TCV-116)
    • Shibouta Y., Inada Y., Ojima M., Wada T., Noda M., Sanada T., Kubo K., Kohara Y., Naka T., Nishikawa K. Pharmacological profile of a highly potent and long-acting angiotensin II receptor antagonist, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole- 7-carboxylic acid (CV-11974), and its prodrug, (±)-1-(cyclohexyloxycarbonyloxy)-ethyl-2-ethoxy-1-[ [ 2′-(1H-tetrazol-5-yl)biphenyl-4-yl ] methyl ]-1H-benzimidazole-7-carboxylate (TCV-116). J Pharmacol Exp Ther. 266:1993;114-120.
    • (1993) J Pharmacol Exp Ther , vol.266 , pp. 114-120
    • Shibouta, Y.1    Inada, Y.2    Ojima, M.3    Wada, T.4    Noda, M.5    Sanada, T.6    Kubo, K.7    Kohara, Y.8    Naka, T.9    Nishikawa, K.10
  • 23
    • 0025086862 scopus 로고
    • Nonpeptide angiotensin receptor antagonists. XI. Pharmacology of EXP3174: An active metabolite of DuP 753, an orally active antihypertensive agent
    • Wong P.C., Price A.W., Chiu A.T., Duncia J.V., Carini D.J., Wexler R., Johnson A., Timmermans P.B. Nonpeptide angiotensin receptor antagonists. XI. Pharmacology of EXP3174 An active metabolite of DuP 753, an orally active antihypertensive agent . J Pharmacol Exp Ther. 255:1990;211-217.
    • (1990) J Pharmacol Exp Ther , vol.255 , pp. 211-217
    • Wong, P.C.1    Price, A.W.2    Chiu, A.T.3    Duncia, J.V.4    Carini, D.J.5    Wexler, R.6    Johnson, A.7    Timmermans, P.B.8
  • 24
    • 0009644628 scopus 로고
    • Some quantitative uses of drugs antagonists
    • Arunlakshana O., Schild H.O. Some quantitative uses of drugs antagonists. Br J Pharmacol. 14:1959;48-52.
    • (1959) Br J Pharmacol , vol.14 , pp. 48-52
    • Arunlakshana, O.1    Schild, H.O.2
  • 25
    • 0027070825 scopus 로고
    • Different type of receptor interaction of peptide and nonpeptide angiotensin II antagonists revealed by receptor binding and functional studies
    • Wienen W., Mauz A.B., Van Meel J.C., Entzeroth M. Different type of receptor interaction of peptide and nonpeptide angiotensin II antagonists revealed by receptor binding and functional studies. Mol Pharmacol. 41:1992;1081-1088.
    • (1992) Mol Pharmacol , vol.41 , pp. 1081-1088
    • Wienen, W.1    Mauz, A.B.2    Van Meel, J.C.3    Entzeroth, M.4
  • 26
    • 0031010320 scopus 로고    scopus 로고
    • A review of mutagenesis studies of angiotensin II type 1 receptor, the three-dimensional receptor model in search of the agonist and antagonist binding site and the hypothesis of a receptor activation mechanism
    • Inoue Y., Nakamura N., Inagami T. A review of mutagenesis studies of angiotensin II type 1 receptor, the three-dimensional receptor model in search of the agonist and antagonist binding site and the hypothesis of a receptor activation mechanism. J Hyperten. 15:1997;703-714.
    • (1997) J Hyperten , vol.15 , pp. 703-714
    • Inoue, Y.1    Nakamura, N.2    Inagami, T.3
  • 28
    • 0028235782 scopus 로고
    • Differentiation between binding sites for angiotensin II and non-peptide antagonists on the angiotensin II type 1 receptors
    • Schambye H.T., Hjorth S.A., Bergsma D.J., Sathe G., Schwartz T.W. Differentiation between binding sites for angiotensin II and non-peptide antagonists on the angiotensin II type 1 receptors. Proc Natl Acad Sci U S A. 91:1994;7046-7050.
    • (1994) Proc Natl Acad Sci U S a , vol.91 , pp. 7046-7050
    • Schambye, H.T.1    Hjorth, S.A.2    Bergsma, D.J.3    Sathe, G.4    Schwartz, T.W.5
  • 29
    • 0030218059 scopus 로고    scopus 로고
    • Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation
    • Kostenis E., Mohr K. Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation. Trends Pharmacol Sci. 17:1996;280-283.
    • (1996) Trends Pharmacol Sci , vol.17 , pp. 280-283
    • Kostenis, E.1    Mohr, K.2
  • 30
    • 0025862043 scopus 로고
    • Nonpeptide angiotensin II receptor antagonists: Insurmountable angiotensin II antagonism of EXP3892 is reversed by the surmountable antagonist DuP 753
    • Wong P.C., Timmermans P.B. Nonpeptide angiotensin II receptor antagonists Insurmountable angiotensin II antagonism of EXP3892 is reversed by the surmountable antagonist DuP 753 . J Pharmacol Exp Ther. 258:1991;49-57.
    • (1991) J Pharmacol Exp Ther , vol.258 , pp. 49-57
    • Wong, P.C.1    Timmermans, P.B.2
  • 33
    • 0003777368 scopus 로고    scopus 로고
    • A short course on theory and methods
    • L.E. Limbird. Boston: Kluwer Academic Publishing
    • Limbird L.E. A short course on theory and methods. Limbird L.E. Cell Surface Receptors. 1996;61-122 Kluwer Academic Publishing, Boston.
    • (1996) Cell Surface Receptors , pp. 61-122
    • Limbird, L.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.