Nα-Z-Nδ-trityl-L-glutamine
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Nα-Z-Nδ-trityl-L-glutamine

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Category
CBZ-Amino Acids
Catalog number
BAT-003245
CAS number
132388-60-4
Molecular Formula
C32H30N2O5
Molecular Weight
522.60
Nα-Z-Nδ-trityl-L-glutamine
IUPAC Name
(2S)-5-oxo-2-(phenylmethoxycarbonylamino)-5-(tritylamino)pentanoic acid
Synonyms
Z-L-Gln(Trt)-OH; (S)-2-(((Benzyloxy)Carbonyl)Amino)-5-Oxo-5-(Tritylamino)Pentanoic Acid
Appearance
White powder
Purity
≥ 99.5% (Chiral HPLC)
Density
1.237±0.06 g/cm3(Predicted)
Melting Point
160-165 °C
Boiling Point
792.6±60.0 °C(Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C32H30N2O5/c35-29(22-21-28(30(36)37)33-31(38)39-23-24-13-5-1-6-14-24)34-32(25-15-7-2-8-16-25,26-17-9-3-10-18-26)27-19-11-4-12-20-27/h1-20,28H,21-23H2,(H,33,38)(H,34,35)(H,36,37)/t28-/m0/s1
InChI Key
MYOAIKMOWHPBQS-NDEPHWFRSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CCC(=O)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)O

Nα-Z-Nδ-trityl-L-glutamine, a protected derivative of the amino acid glutamine, widely utilized in peptide synthesis, offers a myriad of applications. Here are four key applications of Nα-Z-Nδ-trityl-L-glutamine:

Peptide Synthesis: Acting as a fundamental building block in peptide synthesis, Nα-Z-Nδ-trityl-L-glutamine plays a crucial role in meticulously assembling peptide chains. The protective groups Nα-Z and Nδ-trityl serve to shield against unwanted side reactions, ensuring the precise formation of peptide bonds.

Pharmaceutical Development: Within the realm of pharmaceuticals, Nα-Z-Nδ-trityl-L-glutamine emerges as a pivotal component in the creation of peptide-based drugs. Its significance lies in its ability to construct complex peptide sequences required for novel therapeutics targeting a diverse array of entities like hormones or enzymes. By streamlining the synthesis of intricate peptides, this compound plays an instrumental role in driving forward drug discovery and propelling the development of cutting-edge pharmaceutical interventions.

Biochemical Research: Delving into the intricate world of protein and enzyme structure and function, researchers leverage Nα-Z-Nδ-trityl-L-glutamine to unravel critical insights. By incorporating this compound into synthetic peptides, scientists probe the impact of specific amino acid modifications on protein activity, shedding light on the dynamic nature of proteins. This pursuit not only enhances our comprehension of protein dynamics but also sets the stage for the advancement of refined protein-based diagnostics and treatments, marking a paradigm shift in biochemistry research.

Proteomics: Nα-Z-Nδ-trityl-L-glutamine assumes a pivotal role in generating labeled peptides essential for mass spectrometry analysis. The protective groups provided by this compound play a crucial role in distinguishing peptides during experiments aimed at unraveling proteins and mapping intricate protein interactions. This critical application serves as a linchpin in deciphering complex biological pathways and unearthing potential biomarkers for a diverse spectrum of diseases, driving the field of proteomics towards groundbreaking discoveries and enhanced understanding.

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