Specification
Description
Fmoc-n-me-arg(mtr)-oh belongs to the family of arginine derivatives and is commonly used as a building block in peptide synthesis. The compound is composed of an Fmoc (9-fluorenylmethyloxycarbonyl) protective group, an arginine residue, and an mtr (4-methoxy-2,3,6-trimethylbenzenesulfonyl) protective group.
Synonyms
Fmoc-n-me-arg(mtr)-OH, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-5-(3-((4-methoxy-2,3,6-trimethylphenyl)sulfonyl)guanidino)pentanoicacid, FMOC-N-ME-ARG-OH
IUPAC Name
(2S)-5-[[amino-[(4-methoxy-2,3,6-trimethylphenyl)sulfonylamino]methylidene]amino]-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]pentanoic acid
Canonical SMILES
CC1=CC(=C(C(=C1S(=O)(=O)NC(=NCCCC(C(=O)O)N(C)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)N)C)C)OC
InChI
1S/C32H38N4O7S/c1-19-17-28(42-5)20(2)21(3)29(19)44(40,41)35-31(33)34-16-10-15-27(30(37)38)36(4)32(39)43-18-26-24-13-8-6-11-22(24)23-12-7-9-14-25(23)26/h6-9,11-14,17,26-27H,10,15-16,18H2,1-5H3,(H,37,38)(H3,33,34,35)/t27-/m0/s1
InChI Key
LNVHMIGZISCVKC-MHZLTWQESA-N
Application
Fmoc-n-me-arg(mtr)-oh has a variety of applications in scientific experiments, including peptide synthesis, drug discovery, and biological assays.
Type
Unusual Amino Acids, N-α-Methyl Amino Acids