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Volumn 19, Issue 42008, 1999, Pages 631-644

Discovery and Design of Novel Vasopresses Hypotensive Pepitide Agonists

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHYPERTENSIVE AGENT; ARGIPRESSIN DERIVATIVE; OXYTOCIN; VASOPRESSIN; VASOPRESSIN RECEPTOR ANTAGONIST; VASOPRESSIN V2 RECEPTOR;

EID: 0033062563     PISSN: 10799893     EISSN: None     Source Type: Journal    
DOI: 10.3109/10799899909036676     Document Type: Article
Times cited : (11)

References (23)
  • 3
    • 0020026845 scopus 로고
    • Design of more potent antagonists of the antidiuretic responses to arginine vasopressin
    • Manning M., Olma A., Klis W. A., Kolodziejczyk A. M., Seto J., Sawyer W. H. Design of more potent antagonists of the antidiuretic responses to arginine vasopressin. J. Med. Chem. 1982; 25: 45 – 50
    • (1982) J. Med. Chem. , vol.25 , pp. 45-50
    • Manning, M.1    Olma, A.2    Klis, W.A.3    Kolodziejczyk, A.M.4    Seto, J.5    Sawyer, W.H.6
  • 4
    • 0029171213 scopus 로고
    • An exploration of the effects of L- and D-Tetrahydroisoquinoline-3-carboxylic acid substitutions at positions 2, 3 and 7 in cyclic and linear antagonists of vasopressin and oxytocin and at position 3 in arginine vasopressin
    • Manning M., Cheng L. L., Stoev S., Bankowski K., Przybylski J., Klis W. A., Sawyer W. H., Wo N. C., Chan W. Y. An exploration of the effects of L- and D-Tetrahydroisoquinoline-3-carboxylic acid substitutions at positions 2, 3 and 7 in cyclic and linear antagonists of vasopressin and oxytocin and at position 3 in arginine vasopressin. J. Peptide Sci. 1995; 1: 66 – 79
    • (1995) J. Peptide Sci. , vol.1 , pp. 66-79
    • Manning, M.1    Cheng, L.L.2    Stoev, S.3    Bankowski, K.4    Przybylski, J.5    Klis, W.A.6    Sawyer, W.H.7    Wo, N.C.8    Chan, W.Y.9
  • 5
    • 0030625001 scopus 로고    scopus 로고
    • Position three in vasopressin antagonist tolerates conformationally restricted and aromatic amino acid substitutions: a striking contrast with vasopressin agonists
    • Manning M., Cheng L. L., Stoev S., Klis W. A., Nawrocka E., Olma A., Sawyer W. H., Wo N. C., Chan W. Y. Position three in vasopressin antagonist tolerates conformationally restricted and aromatic amino acid substitutions: a striking contrast with vasopressin agonists. J. Peptide Sci. 1997; 3: 31 – 46
    • (1997) J. Peptide Sci. , vol.3 , pp. 31-46
    • Manning, M.1    Cheng, L.L.2    Stoev, S.3    Klis, W.A.4    Nawrocka, E.5    Olma, A.6    Sawyer, W.H.7    Wo, N.C.8    Chan, W.Y.9
  • 8
    • 0023708559 scopus 로고
    • Role of vasopressin in cardiovascular regulation
    • Share L. Role of vasopressin in cardiovascular regulation. Physiological Reviews 1988; 68: 1248 – 1284
    • (1988) Physiological Reviews , vol.68 , pp. 1248-1284
    • Share, L.1
  • 10
    • 0025853070 scopus 로고
    • A radioiodinated linear vasopressin antagonist: A ligand with high affinity and specificity for V1a receptors
    • Schmidt A., Audiger S., Barberis C., Jard S., Manning M., Kolodziejczyk A. S., Sawyer W. H. A radioiodinated linear vasopressin antagonist: A ligand with high affinity and specificity for V1a receptors. FEBS Lett. 1991; 282: 77 – 81
    • (1991) FEBS Lett. , vol.282 , pp. 77-81
    • Schmidt, A.1    Audiger, S.2    Barberis, C.3    Jard, S.4    Manning, M.5    Kolodziejczyk, A.S.6    Sawyer, W.H.7
  • 15
    • 0018897308 scopus 로고
    • [1-(β-Mercapto-β,β-cyclopentamethylenepropionic acid), 2-(O-methyl) tyrosine] arginine-vasopressin and [1-(β-Mercapto-β,β-cyclopentamethylenepropionic acid)] arginine-vasopressin, two highly potent antagonists of the vasopressor response to arginine-vasopressin
    • Kruszynski M., Lammek B., Manning M., Seto J., Haldar J., Sawyer W. H. [1-(β-Mercapto-β,β-cyclopentamethylenepropionic acid), 2-(O-methyl) tyrosine] arginine-vasopressin and [1-(β-Mercapto-β,β-cyclopentamethylenepropionic acid)] arginine-vasopressin, two highly potent antagonists of the vasopressor response to arginine-vasopressin. J. Med. Chem. 1980; 23: 364 – 368
    • (1980) J. Med. Chem. , vol.23 , pp. 364-368
    • Kruszynski, M.1    Lammek, B.2    Manning, M.3    Seto, J.4    Haldar, J.5    Sawyer, W.H.6
  • 16
    • 84957417090 scopus 로고
    • A modification of the method of Dale and Laidlaw for standardization of posterior pituitary extract
    • Holton P. A modification of the method of Dale and Laidlaw for standardization of posterior pituitary extract. Br. J. Pharmacol. 1948; 23: 328 – 334
    • (1948) Br. J. Pharmacol. , vol.23 , pp. 328-334
    • Holton, P.1
  • 17
    • 84982328496 scopus 로고
    • PA, a new scale of the measurement of drug antagonism
    • Schild H. O. PA, a new scale of the measurement of drug antagonism. Br. J. Pharmacol. Chemother. 1947; 2: 189 – 206
    • (1947) Br. J. Pharmacol. Chemother. , vol.2 , pp. 189-206
    • Schild, H.O.1
  • 18
    • 0015991040 scopus 로고
    • [1-β-Mercapto-β,β-diethylpropionic acid]-8-lysine-vasopressin, a potent inhibitor of 8-lysine-vasopressin and oxytocin
    • Dykes D. F., Nestor J. J., Jr., Ferger M. F., du Vigneaud V. [1-β-Mercapto-β,β-diethylpropionic acid]-8-lysine-vasopressin, a potent inhibitor of 8-lysine-vasopressin and oxytocin. J. Med. Chem. 1974; 17: 250 – 252
    • (1974) J. Med. Chem. , vol.17 , pp. 250-252
    • Dykes, D.F.1    Nestor, J.J.2    Ferger, M.F.3    du Vigneaud, V.4
  • 19
    • 0000918627 scopus 로고
    • Biologic assays for oxytocin and vasopressin
    • Sawyer W. H. Biologic assays for oxytocin and vasopressin. Methods Med. Res. 1961; 9: 210 – 219
    • (1961) Methods Med. Res. , vol.9 , pp. 210-219
    • Sawyer, W.H.1
  • 20
    • 0001641316 scopus 로고
    • The quantitative assay of vasopressin
    • Dekanski J. The quantitative assay of vasopressin. Br. J. Pharmacol. 1952; 7: 567 – 572
    • (1952) Br. J. Pharmacol. , vol.7 , pp. 567-572
    • Dekanski, J.1
  • 21
    • 72849154573 scopus 로고
    • Effect of magnesium ion on the response of the rat uterus to neurohypophysial hormones and analogues
    • Munsick R. A. Effect of magnesium ion on the response of the rat uterus to neurohypophysial hormones and analogues. Endocrinology 1960; 66: 451 – 457
    • (1960) Endocrinology , vol.66 , pp. 451-457
    • Munsick, R.A.1
  • 22
    • 0001611730 scopus 로고
    • Solid-phase peptide synthesis. III. An improved synthesis of Bradykinin
    • Merrifield R. B. Solid-phase peptide synthesis. III. An improved synthesis of Bradykinin. Biochemistry 1964; 3: 1385 – 1390
    • (1964) Biochemistry , vol.3 , pp. 1385-1390
    • Merrifield, R.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.