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Chem Impex
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Product Information

Product Name
Na-Fmoc- Nd-trityl-L-glutamine
Brand Name
Chem Impex
Product Number
02411
CAS
132327-80-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
10919157
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoic acid
InChI Key
WDGICUODAOGOMO-DHUJRADRSA-N
SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NC(=O)CCC@@H(C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46

Application

Na-Fmoc- Nd-trityl-L-glutamine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of specific amino acids in a controlled manner, which is essential for developing therapeutic peptides.

Drug Development: It plays a significant role in the pharmaceutical industry for creating novel drug candidates, particularly in the design of peptide-based drugs that can target specific biological pathways.

Bioconjugation: Researchers use this compound to facilitate bioconjugation processes, linking peptides to other biomolecules, which enhances the efficacy of drugs and diagnostic agents.

Protein Engineering: It is employed in protein engineering applications, where modifications to amino acid sequences are necessary to improve protein stability and functionality.

Research in Neuroscience: The compound is utilized in studies related to neurotransmitter functions, helping researchers understand the role of specific peptides in neurological processes.

References Data Source From Pubchem

Potential Enhancement of Topical Drug Delivery Using Grapefruit-derived Nanoparticles Modified Using TAT Peptide

Publication Name: Pharmaceutical Research
Publication Date: 2026-01-21
DOI: 10.1007/s11095-026-04014-6

Discordance between in silico and in vitro results on proteolytic stability of milk protein-derived DPP-4 inhibitory peptides

Publication Name: European Food Research and Technology
Publication Date: 2025-07-09
DOI: 10.1007/s00217-025-04833-8

Stabilization of a miniprotein fold by an unpuckered proline surrogate

Publication Name: Communications Chemistry
Publication Date: 2025-03-12
DOI: 10.1038/s42004-025-01474-6

Parallel Synthesis of Glycopeptide Libraries Using Glyco-SPOT Synthesis

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4578-9_12

Chemoproteomic identification of a DPP4 homolog in Bacteroides thetaiotaomicron

Publication Name: Nature Chemical Biology
Publication Date: 2023-06-22
DOI: 10.1038/s41589-023-01357-8