Nα-Fmoc-Nγ-trityl-L-asparagine
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Nα-Fmoc-Nγ-trityl-L-asparagine

* 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-003678
CAS number
132388-59-1
Molecular Formula
C38H32N2O5
Molecular Weight
596.70
Nα-Fmoc-Nγ-trityl-L-asparagine
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-(tritylamino)butanoic acid
Synonyms
Fmoc-L-Asn(Trt)-OH; (S)-2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)-4-Oxo-4-(Tritylamino)Butanoic Acid
Appearance
White powder
Purity
≥ 99.7% (Chiral HPLC)
Density
1.271±0.06 g/cm3(Predicted)
Melting Point
200-220 °C
Boiling Point
858.1±65.0 °C(Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C38H32N2O5/c41-35(40-38(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28)24-34(36(42)43)39-37(44)45-25-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33/h1-23,33-34H,24-25H2,(H,39,44)(H,40,41)(H,42,43)/t34-/m0/s1
InChI Key
KJYAFJQCGPUXJY-UMSFTDKQSA-N
Canonical SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NC(=O)CC(C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46

Nα-Fmoc-Nγ-trityl-L-asparagine, a protected amino acid derivative, plays a pivotal role in peptide synthesis and biochemical research. Here are four key applications of this compound presented with high perplexity and burstiness: Solid-Phase Peptide Synthesis (SPPS): Serving as a cornerstone in SPPS, Nα-Fmoc-Nγ-trityl-L-asparagine allows for the construction of peptides with unparalleled purity and specificity. Its dual protection shields the amino and side chain functional groups, safeguarding against undesired reactions during peptide assembly. This dual defense ensures precise integration into the growing peptide chain, facilitating the synthesis of intricate peptide sequences.

Protein Engineering: Pioneers in the field of protein manipulation harness Nα-Fmoc-Nγ-trityl-L-asparagine to engineer proteins with novel functionalities or enhanced properties. The compound’s safeguarded state enables selective deprotection and subsequent enhancements at specific protein sites. This technique is pivotal for crafting innovative protein conjugates, investigating protein interactions, and designing cutting-edge biomaterials.

Antigen Production: In the realm of immunological research, Nα-Fmoc-Nγ-trityl-L-asparagine is instrumental in crafting peptide antigens to mimic pathogen epitopes. By constructing peptide sequences that mirror pathogenic markers, researchers generate antigens vital for vaccine development and antibody production. This advancement contributes significantly to the progression of immunotherapy and infectious disease research.

Drug Discovery: A linchpin in drug innovation, Nα-Fmoc-Nγ-trityl-L-asparagine aids in the creation of peptide-based drug candidates. By incorporating this protected amino acid into peptide libraries, scientists conduct screenings to identify bioactive peptides with therapeutic potential. This screening process accelerates the discovery of lead compounds for various diseases, propelling the frontier of peptide-based therapeutics.

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