Fmoc-Arg(Alloc)2-OH
Need Assistance?
  • US & Canada:
    +
  • UK: +

Fmoc-Arg(Alloc)2-OH

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
Fmoc-Amino Acids
Catalog number
BAT-005292
CAS number
148893-34-9
Molecular Formula
C29H32N4O8
Molecular Weight
564.59
Fmoc-Arg(Alloc)2-OH
IUPAC Name
(2S)-5-[bis(prop-2-enoxycarbonylamino)methylideneamino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
Synonyms
(2S)-5-[bis(prop-2-enoxycarbonylamino)methylideneamino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
Purity
≧ 95%
Density
1.290±0.100 g/cm3
Storage
Store at 2-8 °C
InChI
InChI=1S/C29H32N4O8/c1-3-16-39-28(37)32-26(33-29(38)40-17-4-2)30-15-9-14-24(25(34)35)31-27(36)41-18-23-21-12-7-5-10-19(21)20-11-6-8-13-22(20)23/h3-8,10-13,23-24H,1-2,9,14-18H2,(H,31,36)(H,34,35)(H2,30,32,33,37,38)/t24-/m0/s1
InChI Key
RSPFZCDVPTYBLY-DEOSSOPVSA-N
Canonical SMILES
C=CCOC(=O)NC(=NCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)NC(=O)OCC=C

Fmoc-Arg(Alloc)2-OH, a protected amino acid derivative pivotal in peptide synthesis, finds diverse applications in bioscience. Here are the key applications:

Peptide Synthesis: Serving as a crucial building block in solid-phase peptide synthesis, Fmoc-Arg(Alloc)2-OH plays a foundational role in crafting peptides. The Fmoc group shields the amino group, while the Alloc groups safeguard the side chain, enabling precise deprotection and elongation processes. This meticulous approach ensures the synthesis of peptides with exceptional purity and fidelity, rendering them ideal for both research exploration and therapeutic interventions.

Medicinal Chemistry: In the realm of drug discovery and development, Fmoc-Arg(Alloc)2-OH emerges as an indispensable tool for synthesizing peptide-based drugs targeting specific receptors or enzymes. Peptides incorporating Fmoc-Arg(Alloc)2-OH can be tailored to optimize stability, bioavailability, and target specificity. These tailored peptides undergo rigorous testing for their efficacy in treating complex diseases such as cancer and metabolic disorders, showcasing the versatility and potential of this approach in modern medicine.

Protein Engineering: By allowing for the precise incorporation of arginine residues into recombinant proteins, Fmoc-Arg(Alloc)2-OH facilitates in-depth exploration of protein structure and functionality. The adaptable protection strategy permits site-specific modifications that preserve the essential integrity and activity of proteins. This capability is paramount in the creation of proteins with innovative characteristics or heightened biological efficacy, opening new avenues for protein-based therapeutics and research applications.

Bioconjugation: The utility of Fmoc-Arg(Alloc)2-OH extends to the realm of bioconjugation, where peptides or proteins are linked to various molecules such as drugs, fluorescent markers, or nanoparticles. The meticulous control over protective groups ensures specific and stable conjugation, preserving the functional groups’ integrity throughout the process. This precise bioconjugation methodology plays a vital role in crafting targeted drug delivery systems and diagnostic tools, underscoring the importance of controlled molecular interactions in advancing biotechnological applications.

Online Inquiry
Verification code
Inquiry Basket