Z-Arg(Z)2-OSu

Z-Arg(Z)2-OSu is a protected arginine derivative in which the α-amino group is masked with a benzyloxycarbonyl (Z/Cbz-type) protecting group and the side-chain guanidinium functionality is protected with two additional Z groups, forming a bis-Z protected guanidine motif. The molecule also contains an activated N-hydroxysuccinimide (OSu) ester at the carboxyl position, while retaining the amino acid backbone with a free carboxyl equivalent as the succinimidyl ester and a benzylic carbamate-linked nitrogen environment. As an amino acid activated ester, it is used as a coupling reagent precursor in peptide synthesis and peptide fragment assembly, where the OSu leaving group supports formation of amide bonds under controlled conditions while the Z-protecting groups help suppress undesired side reactions of the guanidinium and amino functionalities.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP26306

CAS No:132160-73-7

Synonyms/Alias:Z-Arg(Z)2-Osu;C34H35N5O10;7856AH;ZINC150339518;132160-73-7

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M.F/Formula
C34H35N5O10
M.W/Mr.
673.68
Size
5 g;25 g;
InChI
1S/C34H35N5O10/c40-28-18-19-29(41)39(28)49-30(42)27(36-32(43)46-21-24-11-4-1-5-12-24)17-10-20-35-31(37-33(44)47-22-25-13-6-2-7-14-25)38-34(45)48-23-26-15-8-3-9-16-26/h1-9,11-16,27H,10,17-23H2,(H,36,43)(H2,35,37,38,44,45)/t27-/m0/s1
InChI Key
VXTIDXYCZXQJKB-MHZLTWQESA-N
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)C(CCCN=C(NC(=O)OCC2=CC=CC=C2)NC(=O)OCC3=CC=CC=C3)NC(=O)OCC4=CC=CC=C4

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