Boc-L-2-Furylalanine.DCHA
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Boc-L-2-Furylalanine.DCHA

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Category
BOC-Amino Acids
Catalog number
BAT-014111
CAS number
145206-40-2
Molecular Formula
C24H40N2O5
Molecular Weight
436.59
Boc-L-2-Furylalanine.DCHA
IUPAC Name
(2S)-3-(furan-2-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Density
1.2188 (rough estimate)
Boiling Point
406.4°C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H17NO5/c1-12(2,3)18-11(16)13-9(10(14)15)7-8-5-4-6-17-8/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15)/t9-/m0/s1
InChI Key
YWLUWSMJXXBOLV-VIFPVBQESA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC=CO1)C(=O)O

Boc-L-2-FurylalanineDCHA, an amino acid derivative widely embraced in peptide synthesis and biochemical research, showcases a myriad of applications. Here are the key applications presented with high perplexity and burstiness:

Peptide Synthesis: Serving as a pivotal building block in the intricate world of peptide synthesis, Boc-L-2-FurylalanineDCHA stands out for its unique furyl group that imparts additional chemical dimensions, elevating peptide functionality and stability. This compound finds extensive utility in solid-phase peptide synthesis (SPPS) where it plays a crucial role in crafting tailor-made peptides for diverse research and therapeutic ventures.

Drug Development: In the realm of drug discovery, Boc-L-2-FurylalanineDCHA emerges as a game-changer as it can be seamlessly integrated into peptide-based drug candidates to enhance their pharmacokinetic attributes. The presence of the distinctive furyl group bolsters binding affinity and selectivity towards target proteins, making it a valuable asset in shaping novel therapeutics with far-reaching potential in combating a spectrum of diseases.

Protein Engineering: At the cutting edge of protein engineering, Boc-L-2-FurylalanineDCHA shines as a catalyst for modifying and scrutinizing protein functions. By integrating this amino acid into proteins, researchers embark on a journey to unveil the impact of specific chemical alterations on protein activity structure and interactions.

Bioconjugation: Fueling the domain of bioconjugation, Boc-L-2-FurylalanineDCHA plays a pivotal role in crafting hybrid molecules brimming with combined functionalities. This compound seamlessly binds to other biomolecules, such as antibodies, through its reactive groups thereby facilitating targeted delivery of drugs or imaging agents. Such precision in bioconjugation not only propels the frontier of precision medicine but also catalyzes the development of cutting-edge diagnostic tools heralding a new era in healthcare innovation.

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