N-α-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine
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N-α-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine

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

Category
Fluorinated Amino Acids
Catalog number
BAT-002074
Molecular Formula
C23H19N3O6S2
Molecular Weight
497.55
Synonyms
Fmoc-D-Cys(Npys)-OH; N-alpha-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine
Storage
Store at 2-8 °C

N-α-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine, a specialized chemical compound utilized in peptide synthesis, holds significant importance in bioscience. Here are four key applications:

Solid-Phase Peptide Synthesis: Employed in solid-phase peptide synthesis (SPPS), N-α-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine serves as a protected amino acid crucial for the precise assembly of peptide chains. By safeguarding cysteine residues during synthesis, this compound minimizes unwanted side reactions, elevating the yield and purity of synthesized peptides significantly.

Bioconjugation: Within bioconjugation techniques, this compound plays a pivotal role in attaching peptides to various biomolecules for diverse biomedical applications. The use of protective groups enables selective modification of cysteine residues, facilitating the creation of well-defined conjugates essential for developing targeted drug delivery systems, diagnostic tools, and therapeutic agents with pinpoint accuracy.

Pharmaceutical Research: In the realm of pharmaceutical research, N-α-(9-Fluorenylmethoxycarbonyl)-S-(3-nitro-2-pyridinesulfenyl)-D-cysteine is integral to synthesizing peptide-based drugs and investigating their interactions with biological targets. The precision afforded by this compound aids in crafting peptides capable of acting as inhibitors, agonists, or modulatory agents in disease pathways, pivotal for shaping the landscape of novel and effective peptide therapeutics.

Protein Engineering: This compound finds application in protein engineering endeavors, wherein peptides are synthesized and integrated into larger proteins to explore structure-function relationships in-depth. The selective protection and deprotection of cysteine residues empower researchers to introduce site-specific modifications crucial for unraveling the intricacies of protein folding, stability, and interactions with other molecules, propelling advancements in the field of protein engineering and biotechnology.

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