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Chem Impex
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Product Information

Product Name
Na-Boc-Ne-Z-L-lysine
Brand Name
Chem Impex
Product Number
01364
CAS
2389-45-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2724765
IUPAC Name
(2S)-2-(2-methylpropan-2-yl)oxycarbonylamino-6-(phenylmethoxycarbonylamino)hexanoic acid
InChI Key
BDHUTRNYBGWPBL-HNNXBMFYSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CCCCNC(=O)OCC1=CC=CC=C1)C(=O)O

Application

Na-Boc-Ne-Z-L-lysine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block for synthesizing peptides, allowing researchers to create complex structures for drug development and biological studies.

Bioconjugation: It is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of targeted drug delivery systems.

Protein Engineering: Researchers use it to modify proteins, improving their stability and functionality, which is essential in developing therapeutic proteins and enzymes.

Diagnostics: The compound plays a role in the development of diagnostic tools, particularly in assays that require specific peptide interactions, aiding in disease detection.

Research on Drug Resistance: It is utilized in studies aimed at understanding and overcoming drug resistance in cancer treatments, providing insights that can lead to more effective therapies.

References Data Source From Pubchem

Tumor accumulation in polyethylene glycol-modified dendrimers with enhanced hydration

Publication Name: NPG Asia Materials
Publication Date: 2025-11-28
DOI: 10.1038/s41427-025-00628-1

Antibacterial activity and mechanism of optimized THPA conjugated dipeptides against methicillin-resistant Staphylococcus aureus

Publication Name: The Journal of Antibiotics
Publication Date: 2025-11-10
DOI: 10.1038/s41429-025-00877-w

Identification, Synthesis, and Control Strategy of Process-Related Impurities in the Development and Manufacturing of Bis-Boc-Lisdexamfetamine

Publication Name: Russian Journal of General Chemistry
Publication Date: 2025-10
DOI: 10.1134/s1070363225605010

Synthesis Protocols for Simple Uncharged Glycol Carbamate Nucleic Acids

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2019
DOI: 10.1007/978-1-4939-9216-4_6

Dipeptides as linker for multicomponent presentation—a facile, robust, and high-bioactivity yielding strategy

Publication Name: Medicinal Chemistry Research
Publication Date: 2018-03-23
DOI: 10.1007/s00044-018-2168-y