$21.30

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI01364_5_G
Chem Impex
Get Bulk Quote

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

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

Sequential Multiple Ugi Reactions for the Assembly of Macromulticycles

Publication Name: Science of Synthesis
Publication Date: 2013

α-amino acid pendant polymers as endosomal pH-responsive gene carriers

Publication Name: Macromolecular Research
Publication Date: 2012-03-29
DOI: 10.1007/s13233-012-0057-7