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Volumn 5, Issue 3, 1999, Pages 141-153

An investigation of position 3 in arginine vasopressin with aliphatic, aromatic, conformationally-restricted, polar and charged amino acids

Author keywords

Agonist; Aliphatic; Aromatic; Charged amino acids; Conformationally restricted; Polar

Indexed keywords

2 AMINOBUTYRIC ACID; ALANINE; ARGIPRESSIN DERIVATIVE; AROMATIC AMINO ACID; ASPARTIC ACID; GLYCINE; LEUCINE; NORLEUCINE; NORVALINE; OXYTOCIC AGENT; PHENYLALANINE; PROLINE; SERINE; THREONINE; TRYPTOPHAN; TYROSINE; VALINE; VASOPRESSIN V1 RECEPTOR; VASOPRESSIN V2 RECEPTOR;

EID: 0032956960     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1387(199903)5:3<141::AID-PSC180>3.0.CO;2-6     Document Type: Article
Times cited : (16)

References (63)
  • 1
    • 0000219437 scopus 로고
    • A synthetic preparation possessing biological properties associated with arginine-vasopressin
    • V. du Vigneaud, D.T. Gish and P.G. Katsoyannis (1954). A synthetic preparation possessing biological properties associated with arginine-vasopressin. J. Am. Chem. Soc. 76, 4751-5752.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 4751-5752
    • Du Vigneaud, V.1    Gish, D.T.2    Katsoyannis, P.G.3
  • 3
    • 0004725589 scopus 로고
    • Basic pharmacological properties of synthetic analogues and homologues of the neurohypophysial hormones
    • B. Berde, Ed., Springer Verlag, Berlin
    • B. Berde and R.A. Boissonnas. Basic pharmacological properties of synthetic analogues and homologues of the neurohypophysial hormones, in: Neurohypophysial Hormones and Similar Polypeptides. Handbook of Experimental Pharmacology, Vol. 23, B. Berde, Ed., p. 802-870, Springer Verlag, Berlin, 1968.
    • (1968) Neurohypophysial Hormones and Similar Polypeptides. Handbook of Experimental Pharmacology , vol.23 , pp. 802-870
    • Berde, B.1    Boissonnas, R.A.2
  • 4
    • 0000545447 scopus 로고
    • Tables of analogs
    • K. Jost, M. Lebl and F. Brtnik, Eds. CRC Press, Boca Raton, FL
    • M. Lebl, K. Jost and F. Brtnik. Tables of analogs, in: Handbook of Neurohypophysial Hormone Analogs, Vol. 2, Part 2, K. Jost, M. Lebl and F. Brtnik, Eds, p. 127-267. CRC Press, Boca Raton, FL, 1987.
    • (1987) Handbook of Neurohypophysial Hormone Analogs , vol.2 , Issue.2 PART , pp. 127-267
    • Lebl, M.1    Jost, K.2    Brtnik, F.3
  • 5
    • 0003372827 scopus 로고
    • Structure-activity relationships of neurohypophysial peptides
    • S. Udenfriend and J. Meienhofer, Eds. Academic Press, Orlando, FL
    • V. Hruby and C.W. Smith. Structure-activity relationships of neurohypophysial peptides, in: The Peptides, Vol. 8, S. Udenfriend and J. Meienhofer, Eds, p. 77-207. Academic Press, Orlando, FL, 1987.
    • (1987) The Peptides , vol.8 , pp. 77-207
    • Hruby, V.1    Smith, C.W.2
  • 9
    • 0018666457 scopus 로고
    • Hormonal stimulation of phosphatidylinositol breakdown, with particular reference to the hepatic effects of vasopressin
    • R.H. Michell, C.J. Kirk and M.M. Billah (1979). Hormonal stimulation of phosphatidylinositol breakdown, with particular reference to the hepatic effects of vasopressin. Biochem. Soc. Trans. 7, 861-865.
    • (1979) Biochem. Soc. Trans. , vol.7 , pp. 861-865
    • Michell, R.H.1    Kirk, C.J.2    Billah, M.M.3
  • 10
    • 0023476138 scopus 로고
    • Neurohypophysial hormone receptor systems in brain and periphery
    • S. Jard, C. Barberis, S. Audigier and E. Tribollet (1987). Neurohypophysial hormone receptor systems in brain and periphery. Prog. Brain Res. 72, 173-187.
    • (1987) Prog. Brain Res. , vol.72 , pp. 173-187
    • Jard, S.1    Barberis, C.2    Audigier, S.3    Tribollet, E.4
  • 11
    • 0029837656 scopus 로고    scopus 로고
    • Vasopressin and oxytocin receptors in the central nervous system
    • C. Barberis and E. Tribollet (1996). Vasopressin and oxytocin receptors in the central nervous system. Crit. Rev. Neurobiol. 10, 119-154.
    • (1996) Crit. Rev. Neurobiol. , vol.10 , pp. 119-154
    • Barberis, C.1    Tribollet, E.2
  • 19
    • 0010551486 scopus 로고
    • Arginine-vasotocin, a synthetic analogue of the posterior pituitary hormones containing the ring of oxytocin and the side chain of vasopressin
    • P.G. Katsoyannis and V. du Vigneaud (1958). Arginine-vasotocin, a synthetic analogue of the posterior pituitary hormones containing the ring of oxytocin and the side chain of vasopressin. J. Biol. Chem. 233, 1352-1354.
    • (1958) J. Biol. Chem. , vol.233 , pp. 1352-1354
    • Katsoyannis, P.G.1    Du Vigneaud, V.2
  • 20
    • 0015622907 scopus 로고
    • Solid-phase synthesis and some pharmacological properties of 4-threonine analogs of vasopressins and vasotocin and of arginine-vasopressin and arginine-vasotocin
    • M. Manning, E.J. Coy, W. H. Sawyer and M. Acosta (1973). Solid-phase synthesis and some pharmacological properties of 4-threonine analogs of vasopressins and vasotocin and of arginine-vasopressin and arginine-vasotocin. J. Med. Chem. 16, 463-466.
    • (1973) J. Med. Chem. , vol.16 , pp. 463-466
    • Manning, M.1    Coy, E.J.2    Sawyer, W.H.3    Acosta, M.4
  • 21
    • 84981838296 scopus 로고
    • 8-oxytocine (lysine-vasotocine) et nouvelle synthèse de la lysine-vasopressine
    • 8-oxytocine (lysine-vasotocine) et nouvelle synthèse de la lysine-vasopressine. Helv. Chim. Acta 43, 182-190.
    • (1960) Helv. Chim. Acta , vol.43 , pp. 182-190
    • Boissonnas, R.A.1    Huguenin, R.L.2
  • 22
    • 2442735643 scopus 로고
    • Lysine-vasotocin, a synthetic analog of the posterior pituitary hormones containing the ring of oxytocin and the side chain of lysine-vasopressin
    • R.D. Kimbrough, Jr. and V. du Vigneaud (1961). Lysine-vasotocin, a synthetic analog of the posterior pituitary hormones containing the ring of oxytocin and the side chain of lysine-vasopressin. J. Biol. Chem. 236, 778-780.
    • (1961) J. Biol. Chem. , vol.236 , pp. 778-780
    • Kimbrough Jr., R.D.1    Du Vigneaud, V.2
  • 23
    • 84981841770 scopus 로고
    • Synthèse d'analogues de l'oxytocine et de la lysine-vasopressine contenant de la phénylalanine ou de la tyrosine en position 2 et 3
    • R.A. Boissonnas and S. Guttmann (1960). Synthèse d'analogues de l'oxytocine et de la lysine-vasopressine contenant de la phénylalanine ou de la tyrosine en position 2 et 3. Helv. Chim. Acta 43, 190-200.
    • (1960) Helv. Chim. Acta , vol.43 , pp. 190-200
    • Boissonnas, R.A.1    Guttmann, S.2
  • 24
    • 84981836044 scopus 로고
    • Synthèse de dix analogues de l'oxytocine et de la lysine-vasopressine, contenant de la serine, de l'histidine ou du tryptophane en position 2 ou 3
    • S. Guttmann and R.A. Boissonnas (1960). Synthèse de dix analogues de l'oxytocine et de la lysine-vasopressine, contenant de la serine, de l'histidine ou du tryptophane en position 2 ou 3. Helv. Chim. Acta 43, 200-216.
    • (1960) Helv. Chim. Acta , vol.43 , pp. 200-216
    • Guttmann, S.1    Boissonnas, R.A.2
  • 25
    • 0016742593 scopus 로고
    • Synthesis and some pharmacological properties of [3-β-(2-thienyl)-L-alanine]-8-lysine-vasopressin
    • C.W. Smith, F.M. Ferger and W.Y. Chan (1975). Synthesis and some pharmacological properties of [3-β-(2-thienyl)-L-alanine]-8-lysine-vasopressin. J. Med. Chem. 18, 822-825.
    • (1975) J. Med. Chem. , vol.18 , pp. 822-825
    • Smith, C.W.1    Ferger, F.M.2    Chan, W.Y.3
  • 26
    • 0022260388 scopus 로고
    • Synthesis and biological activities of a fluorescent photoaffinity analog of vasopressin
    • A. Buku, I.L. Schwartz, D. Gazis, C.L. Ma and P. Eggena (1985). Synthesis and biological activities of a fluorescent photoaffinity analog of vasopressin. Endocrinology 117, 196-200.
    • (1985) Endocrinology , vol.117 , pp. 196-200
    • Buku, A.1    Schwartz, I.L.2    Gazis, D.3    Ma, C.L.4    Eggena, P.5
  • 27
    • 0000405059 scopus 로고
    • Synthesis and biological properties of vasopressin analogues containing 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
    • Z. Prochazka, J.E. Anacanas, J. Slaninova, A. Machova, T. Barth and M. Lebl (1990). Synthesis and biological properties of vasopressin analogues containing 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. Collect. Czech. Chem. Commun. 55, 1099-1105.
    • (1990) Collect. Czech. Chem. Commun. , vol.55 , pp. 1099-1105
    • Prochazka, Z.1    Anacanas, J.E.2    Slaninova, J.3    Machova, A.4    Barth, T.5    Lebl, M.6
  • 28
    • 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
    • M. Manning, L.L. Cheng, S. Stoev, K. Bankowski, J. Przybylski. W.A. Klis, W.H. Sawyer, N.C. Wo and W.Y. Chan (1995). 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. 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
  • 29
    • 0020026845 scopus 로고
    • Design of more potent antagonists of the antidiuretic response to arginine vasopressin
    • M. Manning, A. Olma, W.A. Klis, A. Kolodziejczyk, J. Seto and W.H. Sawyer (1982). Design of more potent antagonists of the antidiuretic response to arginine vasopressin. J. Med. Chem. 25, 45-50.
    • (1982) J. Med. Chem. , vol.25 , pp. 45-50
    • Manning, M.1    Olma, A.2    Klis, W.A.3    Kolodziejczyk, A.4    Seto, J.5    Sawyer, W.H.6
  • 30
    • 0030625001 scopus 로고    scopus 로고
    • Position three in vasopressin antagonist tolerates conformationally restricted and aromatic amino acid substitutions: A striking contrast with vasopressin agonists
    • M. Manning, L.L. Cheng, S. Stoev, W.A. Klis, E. Nawrocka, A. Olma, W.H. Sawyer, N.C. Wo and W.Y. Chan (1997). Position three in vasopressin antagonist tolerates conformationally restricted and aromatic amino acid substitutions: a striking contrast with vasopressin agonists. J. Peptide Sci. 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
  • 31
    • 0021358634 scopus 로고
    • Immunological and biological characteristics of the vasotocin-llke activity in the head ganglia of gastropod molluscs
    • W.H. Sawyer, I. Deyrup-Olsen and A. W. Martin (1984). Immunological and biological characteristics of the vasotocin-llke activity in the head ganglia of gastropod molluscs. Gen. Comp. Endocrinol. 54, 97-108
    • (1984) Gen. Comp. Endocrinol. , vol.54 , pp. 97-108
    • Sawyer, W.H.1    Deyrup-Olsen, I.2    Martin, A.W.3
  • 32
    • 0029951427 scopus 로고    scopus 로고
    • Surprising pharmacological activity of analogues designed by substitution of position 3 in arginine vasopressin (AVP) and 8-D-arginine vasopressin with L-2-naphthylalanine
    • B. Lammek, E. Konieczna, H.I. Trzeciak, A. Kozlowski, J. Szymkowiak, R. Stojko and G. Kupryszewski (1996). Surprising pharmacological activity of analogues designed by substitution of position 3 in arginine vasopressin (AVP) and 8-D-arginine vasopressin with L-2-naphthylalanine. J. Pharm. Pharmacol. 48, 316-319.
    • (1996) J. Pharm. Pharmacol. , vol.48 , pp. 316-319
    • Lammek, B.1    Konieczna, E.2    Trzeciak, H.I.3    Kozlowski, A.4    Szymkowiak, J.5    Stojko, R.6    Kupryszewski, G.7
  • 34
    • 2442738019 scopus 로고    scopus 로고
    • An investigation of position three in arginine vasopressin (AVP)
    • J.P. Tam, Ed., Mayflower Scientific Ltd., England, in press
    • M. Manning, S. Stoev, L.L. Cheng, A. Olma, W.A. Klis, W.H. Sawyer, N.C. Wo and W.Y. Chan. An investigation of position three in arginine vasopressin (AVP), in: Peptides, J.P. Tam, Ed., Mayflower Scientific Ltd., England, 1998 (in press).
    • (1998) Peptides
    • Manning, M.1    Stoev, S.2    Cheng, L.L.3    Olma, A.4    Klis, W.A.5    Sawyer, W.H.6    Wo, N.C.7    Chan, W.Y.8
  • 35
    • 45949123116 scopus 로고
    • Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin
    • H. Rink (1987). Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin. Tetrahedron Lett. 28, 3787-3790.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 3787-3790
    • Rink, H.1
  • 36
    • 0004980780 scopus 로고
    • 'Reaction procedures and operating techniques' (Chapter 10) and 'Resin cleavage and purification' (Chapter 11)
    • IRL Press, Oxford, New York, Tokyo
    • E. Atherton and R.C. Sheppard. 'Reaction procedures and operating techniques' (Chapter 10) and 'Resin cleavage and purification' (Chapter 11), in: Solid Phase Peptide Synthesis: A Practical Approach, IRL Press, Oxford, New York, Tokyo, p. 131-161, 1989.
    • (1989) Solid Phase Peptide Synthesis: A Practical Approach , pp. 131-161
    • Atherton, E.1    Sheppard, R.C.2
  • 37
    • 0025232814 scopus 로고
    • Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids
    • G.B. Fields and R.L. Noble (1990). Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids. Int. J. Peptide Protein Res. 35, 161-214.
    • (1990) Int. J. Peptide Protein Res. , vol.35 , pp. 161-214
    • Fields, G.B.1    Noble, R.L.2
  • 38
    • 20744456789 scopus 로고
    • Solid phase peptide synthesis. I. The synthesis of a tetrapeptide
    • R.B. Merrifield (1963). Solid phase peptide synthesis. I. The synthesis of a tetrapeptide. J. Am. Chem. Soc. 85, 2149-2154.
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 2149-2154
    • Merrifield, R.B.1
  • 39
    • 0022699646 scopus 로고
    • Solid phase peptide synthesis
    • R.B. Merrifield (1986). Solid phase peptide synthesis. Science 232, 341-347.
    • (1986) Science , vol.232 , pp. 341-347
    • Merrifield, R.B.1
  • 41
    • 0014432614 scopus 로고
    • Synthesis by the Merrifield method of a protected nonapeptide amide with the amino acid sequence of oxytocin
    • M. Manning (1968). Synthesis by the Merrifield method of a protected nonapeptide amide with the amino acid sequence of oxytocin. J. Am. Chem. Soc. 90, 1348-1349.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 1348-1349
    • Manning, M.1
  • 42
    • 0014967210 scopus 로고
    • Solid-phase synthesis of [4-threonine]oxytocin. A more potent and specific oxytocic agent than oxytocin
    • M. Manning, E. Coy and W.H. Sawyer (1970). Solid-phase synthesis of [4-threonine]oxytocin. A more potent and specific oxytocic agent than oxytocin. Biochemistry 9, 3925-3929.
    • (1970) Biochemistry , vol.9 , pp. 3925-3929
    • Manning, M.1    Coy, E.2    Sawyer, W.H.3
  • 44
    • 0014704672 scopus 로고
    • New method for the synthesis of peptides: Activation of the carboxyl group with dicyclohexylcarbodiimide by using 1-hydroxy-benzotriazole as additive
    • W. Koenig and R. Geiger (1970). New method for the synthesis of peptides: Activation of the carboxyl group with dicyclohexylcarbodiimide by using 1-hydroxy-benzotriazole as additive. Chem. Ber. 103, 788-798.
    • (1970) Chem. Ber. , vol.103 , pp. 788-798
    • Koenig, W.1    Geiger, R.2
  • 45
    • 0002373313 scopus 로고
    • Active esters of 9-fluorenylmethyloxycarbonyl amino acids and their application in the stepwise lengthening of a pepide chain
    • A. Bodanszky, M. Bodanszky, N. Chandramouli, J.Z. Kwei, J. Martinez and J.C. Tolle (1980). Active esters of 9-fluorenylmethyloxycarbonyl amino acids and their application in the stepwise lengthening of a pepide chain. J. Org. Chem. 45, 72-76.
    • (1980) J. Org. Chem. , vol.45 , pp. 72-76
    • Bodanszky, A.1    Bodanszky, M.2    Chandramouli, N.3    Kwei, J.Z.4    Martinez, J.5    Tolle, J.C.6
  • 46
    • 0001034894 scopus 로고
    • A method of synthesis of long peptide chains using a synthesis of oxytocin as an example
    • M. Bodanszky and V. du Vigneaud (1959). A method of synthesis of long peptide chains using a synthesis of oxytocin as an example. J. Am. Chem. Soc. 81, 5688-5691.
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 5688-5691
    • Bodanszky, M.1    Du Vigneaud, V.2
  • 47
    • 0003359140 scopus 로고
    • Active esters and resins in peptide synthesis
    • M. Bodanszky and J.T. Sheehan (1964). Active esters and resins in peptide synthesis. Chem. Ind., 1423-1424.
    • (1964) Chem. Ind. , pp. 1423-1424
    • Bodanszky, M.1    Sheehan, J.T.2
  • 49
    • 0000046837 scopus 로고
    • A highly potent analogue of oxytocin, desamino-oxytocin
    • D.V. Hope, V.V.S. Murti and V. du Vigneaud (1962). A highly potent analogue of oxytocin, desamino-oxytocin. J. Biol. Chem. 237, 1563-1566.
    • (1962) J. Biol. Chem. , vol.237 , pp. 1563-1566
    • Hope, D.V.1    Murti, V.V.S.2    Du Vigneaud, V.3
  • 50
    • 0017861160 scopus 로고
    • Solid phase synthesis of somatostatin and glucagon-selective analogs in gram quantities
    • J. Rivier, R. Kaiser and R. Galyean (1978). Solid phase synthesis of somatostatin and glucagon-selective analogs in gram quantities. Biopolymers 17, 1927-1938.
    • (1978) Biopolymers , vol.17 , pp. 1927-1938
    • Rivier, J.1    Kaiser, R.2    Galyean, R.3
  • 51
    • 0014402250 scopus 로고
    • The purification of synthetic oxytocin and analogues by gel filtration on Sephadex G-15
    • M. Manning, T.C. Wuu and J.W.M. Baxter (1968). The purification of synthetic oxytocin and analogues by gel filtration on Sephadex G-15. J. Chromatogr. 38, 396-398.
    • (1968) J. Chromatogr. , vol.38 , pp. 396-398
    • Manning, M.1    Wuu, T.C.2    Baxter, J.W.M.3
  • 52
    • 84957417090 scopus 로고
    • A modification of the method of Dale and Laidlaw for standardization of posterior pituitary extract
    • P. Holton (1948). A modification of the method of Dale and Laidlaw for standardization of posterior pituitary extract. Br. J. Pharmacol. 3, 328-334.
    • (1948) Br. J. Pharmacol. , vol.3 , pp. 328-334
    • Holton, P.1
  • 53
    • 0000918627 scopus 로고
    • Biologic assays for oxytocin and vasopressin
    • W.H. Sawyer (1961). Biologic assays for oxytocin and vasopressin. Methods Med. Res. 9, 210-219.
    • (1961) Methods Med. Res. , vol.9 , pp. 210-219
    • Sawyer, W.H.1
  • 54
    • 0001641316 scopus 로고
    • The quantitative assay of vasopressin
    • J. Dekanski (1952). The quantitative assay of vasopressin. Br. J. Pharmacol. 7, 567-572.
    • (1952) Br. J. Pharmacol. , vol.7 , pp. 567-572
    • Dekanski, J.1
  • 55
    • 72849154573 scopus 로고
    • Effect of magnesium ion on the response of the rat uterus to neurohypophysial hormones and analogues
    • R.A. Munsick (1960). Effect of magnesium ion on the response of the rat uterus to neurohypophysial hormones and analogues. Endocrinology 66, 451-457.
    • (1960) Endocrinology , vol.66 , pp. 451-457
    • Munsick, R.A.1
  • 56
    • 0000960777 scopus 로고
    • Synthesis of 1-deamino-8-D-γ-aminobutyrinevasopressin, 1-deamino-8-D-lysine-vasopressin, and 1-deamino-8-D-arginine-vasopressin
    • M. Zaoral, J. Kolc and F. Šorm (1967). Synthesis of 1-deamino-8-D-γ-aminobutyrinevasopressin, 1-deamino-8-D-lysine-vasopressin, and 1-deamino-8-D-arginine-vasopressin. Collect. Czech. Chem. Commun. 32, 1250-1257.
    • (1967) Collect. Czech. Chem. Commun. , vol.32 , pp. 1250-1257
    • Zaoral, M.1    Kolc, J.2    Šorm, F.3
  • 57
    • 0015789667 scopus 로고
    • Solid phase synthesis of [1-deamino,4-valine]-8-D-arginine-vasopressin (dVDAVP), a highly potent and specific antidiuretic agent possessing protracted effects
    • M. Manning, L. Balaspiri, M. Acosta and W.H. Sawyer (1973). Solid phase synthesis of [1-deamino,4-valine]-8-D-arginine-vasopressin (dVDAVP), a highly potent and specific antidiuretic agent possessing protracted effects. J. Med. Chem. 16, 975-978.
    • (1973) J. Med. Chem. , vol.16 , pp. 975-978
    • Manning, M.1    Balaspiri, L.2    Acosta, M.3    Sawyer, W.H.4
  • 58
    • 0343114783 scopus 로고    scopus 로고
    • Discovery of novel selective hypotensive analogues of a vasopressin antagonist
    • Peptides R. Ramage and R. Epton, Eds
    • M. Manning, S. Stoev, N.C. Wo and W.Y. Chan. Discovery of novel selective hypotensive analogues of a vasopressin antagonist, in: Peptides 1996, R. Ramage and R. Epton, Eds, p. 615-616, 1998.
    • (1998) Peptides 1996 , pp. 615-616
    • Manning, M.1    Stoev, S.2    Wo, N.C.3    Chan, W.Y.4
  • 60
    • 33747866223 scopus 로고
    • The preparation of Merrifield-resin through total esterification with cesium salts
    • F. Gisin (1973). The preparation of Merrifield-resin through total esterification with cesium salts. Helv. Chim. Acta 56, 1476-1482.
    • (1973) Helv. Chim. Acta , vol.56 , pp. 1476-1482
    • Gisin, F.1
  • 63
    • 85004899697 scopus 로고
    • Application of BOP reagent in solid phase synthesis. II. Solid phase side-chain to side-chain cyclizations using BOP reagent
    • M. Felix, C.-T. Wang, E.P. Heimer and A. Fournier (1988). Application of BOP reagent in solid phase synthesis. II. Solid phase side-chain to side-chain cyclizations using BOP reagent. Int. J. Peptide Protein Res. 31, 231-238.
    • (1988) Int. J. Peptide Protein Res. , vol.31 , pp. 231-238
    • Felix, M.1    Wang, C.-T.2    Heimer, E.P.3    Fournier, A.4


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