Nα-Fmoc-Nδ-trityl-L-glutamine
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Nα-Fmoc-Nδ-trityl-L-glutamine

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Category
Fmoc-Amino Acids
Catalog number
BAT-003652
CAS number
132327-80-1
Molecular Formula
C39H34N2O5
Molecular Weight
610.70
Nα-Fmoc-Nδ-trityl-L-glutamine
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoic acid
Synonyms
Fmoc-L-Gln(Trt)-OH; (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoic acid
Appearance
White to off-white powder
Purity
≥ 99.8% (Chiral HPLC)
Density
1.256±0.06 g/cm3(Predicted)
Melting Point
165-172 °C
Boiling Point
873.5±65.0 °C(Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C39H34N2O5/c42-36(41-39(27-14-4-1-5-15-27,28-16-6-2-7-17-28)29-18-8-3-9-19-29)25-24-35(37(43)44)40-38(45)46-26-34-32-22-12-10-20-30(32)31-21-11-13-23-33(31)34/h1-23,34-35H,24-26H2,(H,40,45)(H,41,42)(H,43,44)/t35-/m0/s1
InChI Key
WDGICUODAOGOMO-DHUJRADRSA-N
Canonical SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NC(=O)CCC(C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46

Nα-Fmoc-Nδ-trityl-L-glutamine, a derivative of protected amino acid, finds frequent use in peptide synthesis. Here are four key applications of Nα-Fmoc-Nδ-trityl-L-glutamine:

Peptide Synthesis: Acting as a foundational element in solid-phase peptide synthesis (SPPS), Nα-Fmoc-Nδ-trityl-L-glutamine plays a pivotal role. The Fmoc and trityl protective groups meticulously regulate reactions during peptide assembly, enabling chemists to intricately construct peptides with utmost precision. Such precision not only facilitates the creation of complex peptides but also drives advancements in pharmaceutical research and biomedical innovation.

Structural Biology: Within the realm of structural biology, Nα-Fmoc-Nδ-trityl-L-glutamine emerges as a crucial tool for crafting peptides that mimic intricate protein structures. By integrating this amino acid derivative, researchers can stabilize specific peptide conformations, facilitating in-depth exploration of protein folding interactions and functions. This technique deepens our understanding of molecular biology, shedding light on the complexities of biological systems.

Bioconjugation Studies: The versatility of Nα-Fmoc-Nδ-trityl-L-glutamine extends to bioconjugation applications, where it serves to bind peptides to diverse molecules or surfaces. Its distinctive protective groups afford selective modification and linking strategies, pivotal in the development of precise targeted drug delivery systems, diagnostic tools, and biosensors within the realms of medical and biotechnological research.

Pharmaceutical Research: Incorporating Nα-Fmoc-Nδ-trityl-L-glutamine into peptide libraries presents a valuable avenue for screening potential therapeutic candidates in pharmaceutical research. Through the synthesis of varied peptides, researchers can explore interactions and efficacy against specific biological targets, offering crucial insights for drug discovery and the development of innovative treatments across various disease domains.

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