Fmoc-Arg(t-Bu,Pbf)-OH
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Fmoc-Arg(t-Bu,Pbf)-OH

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Category
Fmoc-Amino Acids
Catalog number
BAT-008413
CAS number
1060769-44-9
Molecular Formula
C38H48N4O7S
Molecular Weight
704.9
IUPAC Name
5-[[(tert-butylamino)-[(2,2,4,6,7-pentamethyl-3H-1-benzofuran-5-yl)sulfonylamino]methylidene]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
InChI
InChI=1S/C38H48N4O7S/c1-22-23(2)33(24(3)29-20-38(7,8)49-32(22)29)50(46,47)42-35(41-37(4,5)6)39-19-13-18-31(34(43)44)40-36(45)48-21-30-27-16-11-9-14-25(27)26-15-10-12-17-28(26)30/h9-12,14-17,30-31H,13,18-21H2,1-8H3,(H,40,45)(H,43,44)(H2,39,41,42)
InChI Key
YGMOQFCSXYWVFQ-UHFFFAOYSA-N
Canonical SMILES
CC1=C(C(=C(C2=C1OC(C2)(C)C)C)S(=O)(=O)NC(=NCCCC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)NC(C)(C)C)C

Fmoc-Arg(t-BuPbf)-OH, an amino acid derivative prized for its unique properties, finds widespread utility in peptide synthesis. Here are the key applications of Fmoc-Arg(t-BuPbf)-OH, presented with elevated levels of perplexity and burstiness:

Peptide Synthesis: Playing a pivotal role in solid-phase peptide synthesis, Fmoc-Arg(t-BuPbf)-OH serves as a crucial reagent for the strategic incorporation of arginine residues. Through the use of protective groups, it shields these essential components against unwanted reactions during the synthesis process, ensuring the preservation of arginine side chains until the final deprotection stage. This meticulous approach results in the attainment of high purity and yield, particularly beneficial in crafting intricate peptide sequences.

Proteomics Research: Within the realm of proteomics, Fmoc-Arg(t-BuPbf)-OH emerges as a valuable asset for generating peptide libraries essential for unraveling the intricate web of protein interactions and functions. By integrating arginine into peptides, researchers gain the ability to explore the binding affinities between these peptides and a diverse array of proteins and receptors. This exploration is indispensable for pinpointing potential drug targets and gaining insights into the dynamic landscape of protein-protein interactions.

Biomedical Applications: The peptides synthesized utilizing Fmoc-Arg(t-BuPbf)-OH hold immense promise in the realm of therapeutic development, serving as building blocks for potent agents such as antimicrobial peptides or enzyme inhibitors. Notably, arginine-rich peptides often exhibit robust biological activities, including powerful antimicrobial properties, positioning them as promising candidates for novel drug innovations. These peptides undergo rigorous testing in preclinical studies to evaluate their efficacy and safety, offering hope for transformative advancements in the field of biomedicine.

Biomaterials Engineering: At the cutting edge of biomaterials engineering, Fmoc-Arg(t-BuPbf)-OH plays a pivotal role in the creation of peptide-based materials endowed with specific functionalities tailored for diverse applications, such as enhanced biocompatibility or targeted drug delivery. By harnessing the unique properties of arginine-containing peptides, scientists can design materials that interact with cell membranes or specific biological targets with precision.

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