Fmoc-Arg(Pbf)-OMe
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Fmoc-Arg(Pbf)-OMe

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Category
Fmoc-Amino Acids
Catalog number
BAT-001910
CAS number
1998701-23-7
Molecular Formula
C35H42N4O7S
Molecular Weight
662.8
IUPAC Name
methyl (2S)-5-[[amino-[(2,2,4,5,7-pentamethyl-3H-1-benzofuran-6-yl)sulfonylamino]methylidene]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoate
InChI
InChI=1S/C35H42N4O7S/c1-20-21(2)31(22(3)30-27(20)18-35(4,5)46-30)47(42,43)39-33(36)37-17-11-16-29(32(40)44-6)38-34(41)45-19-28-25-14-9-7-12-23(25)24-13-8-10-15-26(24)28/h7-10,12-15,28-29H,11,16-19H2,1-6H3,(H,38,41)(H3,36,37,39)/t29-/m0/s1
InChI Key
AJHUUBFUSQKGKT-LJAQVGFWSA-N
Canonical SMILES
CC1=C(C(=C(C2=C1CC(O2)(C)C)C)S(=O)(=O)NC(=NCCCC(C(=O)OC)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)N)C

Fmoc-Arg(Pbf)-OMe, also known as Fmoc-Arginine(Pbf)-Methyl Ester, plays a crucial role in peptide synthesis with its multifaceted applications in bioscience. Explore the key applications of Fmoc-Arg(Pbf)-OMe presented in a highly perplex and bursty manner:

Peptide Synthesis: Engage in solid-phase peptide synthesis (SPPS) with Fmoc-Arg(Pbf)-OMe, a sought-after amino acid derivative for introducing arginine residues with precision, circumventing undesired side reactions. The Pbf group shields the guanidino side chain of arginine, ensuring the specific formation of peptide bonds. This streamlined process facilitates the accurate assembly of intricate peptides and proteins, revolutionizing synthetic biology.

Drug Development: Dive into the realm of pharmaceutical innovation by harnessing Fmoc-Arg(Pbf)-OMe in synthesizing peptide-based therapeutics. Arginine residues are essential for the biological activity and stability of therapeutic peptides. By leveraging Fmoc-Arg(Pbf)-OMe, researchers can craft novel peptide drugs with enhanced efficacy and pharmacokinetic properties, reshaping the landscape of drug discovery and personalized medicine.

Protein-Protein Interaction Studies: Unveil the intricate world of protein-protein interactions using Fmoc-Arg(Pbf)-OMe to engineer arginine-rich peptides. Arginine residues play a pivotal role in mediating binding and recognition events between proteins. By synthesizing peptides with strategic arginine placements, researchers can delve into these fundamental interactions, shedding light on cellular functions and paving the way for designing innovative inhibitors with targeted precision.

Bioconjugation: Embark on innovative bioconjugation strategies with Fmoc-Arg(Pbf)-OMe, leveraging its ability to introduce arginine residues as functional sites for conjugating biomolecules. These modified peptides can be seamlessly linked to diverse moieties, such as fluorescent labels or therapeutic agents. This facilitates the development of tailored delivery systems and cutting-edge diagnostic tools, amplifying the specificity and sensitivity of biotechnological applications and heralding a new era of precision medicine.

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