Papain-catalyzed fragment synthesis of protected cholecystokinin derivatives
…, P Majer, J Slaninová, J Hlaváček
Index: Cerovsky, Vaclav; Pirkova, Jana; Majer, Pavel; Slaninova, Jirina; Hlavacek, Jan Collection of Czechoslovak Chemical Communications, 1990 , vol. 55, # 7 p. 1873 - 1882
Full Text: HTML
Citation Number: 1
Abstract
Abstract Sodium salts of methyl esters of N-tert-butyloxycarbonyl-β-tert-butylaspartyl-O 4- sulfotyrosine (II) or N-tert-butyloxycarbonyl-O 4-sulfotyrosine (III) were condensed with amino components derived from peptide amides IVb-IVe and IVg (simulating the carboxy- terminal part of cholecystokinin) under catalysis with papain. Rates and yields of conversion of these peptides to the corresponding derivatives Ib-If were compared with the results ...
Related Articles:
[Sakina; Kawazura; Morihara; Yajima Chemical and Pharmaceutical Bulletin, 1988 , vol. 36, # 10 p. 3915 - 3919]
[Sakina; Kawazura; Morihara; Yajima Chemical and Pharmaceutical Bulletin, 1988 , vol. 36, # 10 p. 3915 - 3919]
[Sadovnikova, N. V.; Fedotov, V. P.; Shvachkin, Yu. P.; Shishkina, A. A.; Kolomeitseva, L. A. Pharmaceutical Chemistry Journal, 1987 , vol. 21, # 12 p. 838 - 842 Khimiko-Farmatsevticheskii Zhurnal, 1987 , vol. 21, # 12 p. 1424 - 1427]