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Catalog Number:
07136
CAS Number:
125323-99-1
Nα-Boc-Nε-isopropyl-Nε-Z-L-lysine
Purity:
≥ 95% (HPLC)
Synonym(s):
Boc-L-Lys(iPr,Z)-OH
Documents
$96.34 /250MG
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Product Information

Na-Boc-Ne-isopropyl-Ne-Z-L-lysine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound is particularly valued for its protective Boc (tert-butyloxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis of complex peptides. Its unique structure, featuring both isopropyl and phenylmethoxycarbonyl groups, enhances its stability and solubility, making it an ideal choice for researchers in medicinal chemistry and biochemistry.

In practical applications, Na-Boc-Ne-isopropyl-Ne-Z-L-lysine is commonly utilized in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to serve as a building block in the synthesis of bioactive peptides allows for the exploration of novel therapeutic agents, particularly in the fields of oncology and immunology. Additionally, its favorable properties compared to other amino acid derivatives make it a preferred option for researchers seeking efficiency and reliability in their synthesis processes.

Synonyms
Boc-L-Lys(iPr,Z)-OH
CAS Number
125323-99-1
Purity
≥ 95% (HPLC)
Molecular Formula
C22H34N2O6
Molecular Weight
422.5
MDL Number
MFCD00236860
PubChem ID
14840638
Appearance
Oil
Optical Rotation
[a]20D = 13 ± 2 ° (C=1 in Chloroform)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Lys(iPr,Z)-OH
CAS Number
125323-99-1
Purity
≥ 95% (HPLC)
Molecular Formula
C22H34N2O6
Molecular Weight
422.5
MDL Number
MFCD00236860
PubChem ID
14840638
Appearance
Oil
Optical Rotation
[a]20D = 13 ± 2 ° (C=1 in Chloroform)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective groups facilitate selective reactions, making it easier to construct complex peptide structures.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates. The compound's unique structure allows for modifications that can enhance drug efficacy and specificity, particularly in targeting specific biological pathways.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, where it can be used to attach biomolecules to drugs or imaging agents. This application is crucial in developing targeted therapies and diagnostic tools in medicine.
  • Protein Engineering: Researchers use this compound in protein engineering to modify lysine residues, improving protein stability and functionality. This is particularly beneficial in the production of therapeutic proteins.
  • Research in Cancer Therapy: The compound is being explored in cancer research for its potential to create targeted therapies that can selectively attack cancer cells while minimizing damage to healthy tissues, offering a promising avenue for more effective treatments.

Citations