N-β-Trityl-D-asparagine
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N-β-Trityl-D-asparagine

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Category
D-Amino Acids
Catalog number
BAT-006044
CAS number
200192-49-0
Molecular Formula
C23H22N2O3
Molecular Weight
374.44
N-β-Trityl-D-asparagine
IUPAC Name
(2R)-4-amino-4-oxo-2-(tritylamino)butanoic acid
Synonyms
H-D-Asn(Trt)-OH
Purity
99%
Storage
Store at -20°C
InChI
InChI=1S/C23H22N2O3/c24-21(26)16-20(22(27)28)25-23(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-15,20,25H,16H2,(H2,24,26)(H,27,28)/t20-/m1/s1
InChI Key
QIRPOVMESMPVKL-HXUWFJFHSA-N
Canonical SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NC(CC(=O)N)C(=O)O

N-β-Trityl-D-asparagine, a synthetic amino acid derivative, finds diverse applications in biochemical research and pharmaceutical development. Here are four key applications presented with high perplexity and burstiness:

Peptide Synthesis: A cornerstone in solid-phase peptide synthesis, N-β-Trityl-D-asparagine acts as a protected amino acid, safeguarding the asparagine side chain with its trityl group. This protective measure prevents any unwanted side reactions during peptide bond formation, ensuring the precise synthesis of peptides and proteins, vital for both research and therapeutic advancements.

Protein Engineering: Exploring the realm of protein dynamics, the incorporation of N-β-Trityl-D-asparagine into proteins offers insights into how modifications in the asparagine residue impact protein structure and function. Researchers strategically integrate this derivative into specific protein sites to unravel its implications on stability, folding, and activity—key elements in the design of engineered proteins tailored to exhibit desired properties.

Pharmaceutical Research: A pivotal player in therapeutic peptide development, N-β-Trityl-D-asparagine aids in the synthesis of complex peptide analogs with heightened stability and bioactivity by shielding the asparagine residue from chemical modifications. This unique application propels the design of drugs targeting specific proteins or receptors, paving the way for innovative approaches in drug discovery and personalized medicine.

Chemical Biology: Delving into the nuances of biological processes, N-β-Trityl-D-asparagine serves as a catalyst in creating modified proteins for probing cellular mechanisms. Harnessing this derivative in peptide and protein design, researchers fashion molecular tools indispensable for deciphering biochemical pathways and molecular functions crucial for advancing cell biology and disease research, unveiling the intricacies of life at a molecular level.

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