56.3
[1]. K C Pugh, et al. Synthesis and stability of 3-nitro--pyridinesulfenyl chloride (NpysCl). Int J Pept Protein Res. 1993 Aug;():159-6.
[]. O Rosen, et al. Thiolysis of the 3-nitro--pyridinesulfenyl (Npys) protecting group. An approach towards a general deprotection scheme in peptide synthesis. Int J Pept Protein Res. 199 Jun;35(6):55-9.
[3]. R G Simmonds, et al. Synthesis of disulfide-bridged fragments of omega-conotoxins GVIA and MVIIA. Use of Npys as a protecting/activating group for cysteine in Fmoc syntheses. Int J Pept Protein Res. 199 Apr;3():363-6.
[]. R Matsueda, et al. Compatibility of the S-(3-nitro--pyridinesulfenyl) protecting group with DCC/HOBt coupling chemistry. Pept Res. 199 Sep-Oct;5(5):6-.
[5]. R Matsueda, et al. Design and synthesis of a kininogen-based selective inhibitor of thrombin-induced platelet aggregation. Pept Res. 199 Jan-Feb;7(1):3-5.
H31
P6-P6-P-P31+P33+P331-P3+P3-P363-P5-P51
GHS5
361