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Volumn 53, Issue 1, 1999, Pages 91-97

Removal of iodine by solid phase adsorption to charcoal following iodine oxidation of acetamidomethyl-protected peptide precursors to their disulfide bonded products: Oxytocin and a Pre-S1 peptide of hepatitis B virus illustrate the method

Author keywords

Charcoal; Cystine peptide synthesis; Disulfide bonded peptide from disulfide bond forming reaction mixture; Hepatitis B virus Pre S1 region; Iodine; Oxytocin; S acetamidomethyl cysteine; Solid phase adsorption

Indexed keywords

CHARCOAL; DISULFIDE; IODINE; OXYTOCIN; PEPTIDE;

EID: 0033061086     PISSN: 1397002X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1999.tb01621.x     Document Type: Article
Times cited : (6)

References (9)
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    • 1. Kamber, B., Hartmann, A., Eisler, K. Riniker, B., Rink, H., Sieber, P. & Rittel, W. (1980) The synthesis of cystine peptides by iodine oxidation of S-trityl-cysteine and S-acetamidomethyl-cysteine peptides. Helv. Chim. Acta 63, 899-915.
    • (1980) Helv. Chim. Acta , vol.63 , pp. 899-915
    • Kamber, B.1    Hartmann, A.2    Eisler, K.3    Riniker, B.4    Rink, H.5    Sieber, P.6    Rittel, W.7
  • 2
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    • Efficient solution phase synthesis of {1-(β-mercapto-β, β-cyclopentamethylene propionic acid) -2-(O-ethyl-D-tyrosine) -4-valine-9-desglycine} arginine vasopressin
    • 2. Mendelson, W.L., Tickner, A.M., Holmes, M.M. & Lantos, I. (1990) Efficient solution phase synthesis of {1-(β-mercapto-β, β-cyclopentamethylene propionic acid) -2-(O-ethyl-D-tyrosine) -4-Valine-9-desglycine} arginine vasopressin. Int. J. Peptide Protein Res. 35, 249-257.
    • (1990) Int. J. Peptide Protein Res. , vol.35 , pp. 249-257
    • Mendelson, W.L.1    Tickner, A.M.2    Holmes, M.M.3    Lantos, I.4
  • 4
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    • Comparative evaluation of different methods of disulfide bond formation in synthesis of HIV-2 antigenic determinant
    • 4. Kudryavtseva, E.V., Sidorova, M.V., Ovchinnikov, M.V., Bespalova, Zh.D. & Bushuev, V.N. (1997) Comparative evaluation of different methods of disulfide bond formation in synthesis of HIV-2 antigenic determinant. J. Peptide Res. 49, 52-58.
    • (1997) J. Peptide Res. , vol.49 , pp. 52-58
    • Kudryavtseva, E.V.1    Sidorova, M.V.2    Ovchinnikov, M.V.3    Bespalova, Zh.D.4    Bushuev, V.N.5
  • 5
    • 0030152651 scopus 로고    scopus 로고
    • Syntheses and biological activities of parallel and antiparallel homo and hetero biscystine dimers of oxytocin and deaminooxytocin
    • 5. Chen, L., Bauerova, H., Slaninova, J. & Barany, G. (1996) Syntheses and biological activities of parallel and antiparallel homo and hetero biscystine dimers of oxytocin and deaminooxytocin. Peptide Res. 9, 114-122.
    • (1996) Peptide Res. , vol.9 , pp. 114-122
    • Chen, L.1    Bauerova, H.2    Slaninova, J.3    Barany, G.4
  • 6
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    • Side reaction during the deprotection of (S-acetamidomethyl) cysteine in a peptide with a high serine and threonine content
    • 6. Lamthanh, H., Roumestand, C., Deprun, C. & Menez, A. (1993) Side reaction during the deprotection of (S-acetamidomethyl) cysteine in a peptide with a high serine and threonine content. Int. J. Peptide Protein Res. 41, 85-95.
    • (1993) Int. J. Peptide Protein Res. , vol.41 , pp. 85-95
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    • Synthesis of oxytocin using iodine for oxidative cyclization and silica gel adsorption chromatography for purification
    • 8. Flouret, G., Terada, S., Kato, T., Gualtieri, R. & Lipkowski, A. (1979) Synthesis of oxytocin using iodine for oxidative cyclization and silica gel adsorption chromatography for purification. Int. J. Peptide Protein Res. 13, 137-141.
    • (1979) Int. J. Peptide Protein Res. , vol.13 , pp. 137-141
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  • 9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.