Papain??specific activating esters in aqueous dipeptide synthesis
…, M Mariman, HIV Amatdjais??Groenen…
Index: de Beer, Roseri J.A.C.; Zarzycka, Barbara; Mariman, Michiel; Amatdjais-Groenen, Helene I.V.; Mulders, Marc J.; Quaedflieg, Peter J.L.M.; van Delft, Floris L.; Nabuurs, Sander B.; Rutjes, Floris P.J.T. ChemBioChem, 2012 , vol. 13, # 9 p. 1319 - 1326
Full Text: HTML
Citation Number: 9
Abstract
Abstract Enzymatic peptide synthesis has the potential to be a viable alternative for chemical peptide synthesis. Because of the increasing commercial interest in peptides, new and improved enzymatic synthesis methods are desirable. In recently developed enzymatic strategies such as substrate mimetic approaches and enzyme-specific activation, use of the guanidinophenyl ester (OGp) group has been shown to suffer from some drawbacks. OGp ...
Related Articles:
Optical Rotation of Peptides. VII. α-and γ-Dipeptides of Glutamic Acid and Alanine1
[Sachs; Brand Journal of the American Chemical Society, 1953 , vol. 75, p. 4608]
A shorter synthesis of glutathione
[Goldschmidt,S. et al. Chemische Berichte, 1964 , vol. 97, p. 2434 - 2438]
Optical Rotation of Peptides. VII. α-and γ-Dipeptides of Glutamic Acid and Alanine1
[Sachs; Brand Journal of the American Chemical Society, 1953 , vol. 75, p. 4608]
Optical Rotation of Peptides. VII. α-and γ-Dipeptides of Glutamic Acid and Alanine1
[Sachs; Brand Journal of the American Chemical Society, 1953 , vol. 75, p. 4608]
[Kobayashi, Kazuya; Oishi, Shinya; Kobayashi, Yuka; Ohno, Hiroaki; Tsutsumi, Hiroko; Hata, Yoji; Fujii, Nobutaka Bioorganic and Medicinal Chemistry, 2012 , vol. 20, # 8 p. 2651 - 2655]