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Catalog Number:
12784
CAS Number:
346694-77-7
Nβ-Boc-Nω-Z-L-β-homolysine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-HomoLys(Z)-OH, (S-3-(Boc-amino)-7-(Z-amino)heptanoic acid
Documents
$72.31 /100MG
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Product Information

Nb-Boc-Nw-Z-L-b-homolysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound, characterized by its unique Boc (tert-butyloxycarbonyl) protecting group, enhances the stability and solubility of peptides, making it an essential building block for researchers in medicinal chemistry and biochemistry. Its ability to facilitate the formation of complex peptide structures allows for the exploration of novel therapeutic agents, particularly in the fields of oncology and immunology.

The compound's distinctive structure not only aids in the synthesis of bioactive peptides but also provides advantages in terms of selectivity and reactivity. Researchers have utilized Nb-Boc-Nw-Z-L-b-homolysine in the development of targeted drug delivery systems and in the design of peptide-based vaccines. Its application extends to the creation of enzyme inhibitors and receptor ligands, showcasing its potential in advancing pharmaceutical research. With its robust properties and practical applications, this compound is an invaluable asset for professionals seeking innovative solutions in peptide chemistry.

Synonyms
Boc-L-β-HomoLys(Z)-OH, (S-3-(Boc-amino)-7-(Z-amino)heptanoic acid
CAS Number
346694-77-7
Purity
≥ 98% (HPLC)
Molecular Formula
C20H30N2O6
Molecular Weight
394.47
MDL Number
MFCD01862937
PubChem ID
4393170
Appearance
White solid
Optical Rotation
[a]D25 = - 7 ± 2 º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-β-HomoLys(Z)-OH, (S-3-(Boc-amino)-7-(Z-amino)heptanoic acid
CAS Number
346694-77-7
Purity
≥ 98% (HPLC)
Molecular Formula
C20H30N2O6
Molecular Weight
394.47
MDL Number
MFCD01862937
PubChem ID
4393170
Appearance
White solid
Optical Rotation
[a]D25 = - 7 ± 2 º (C=1 in EtOH)
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

Nb-Boc-Nw-Z-L-b-homolysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for therapeutic applications.
  • Drug Development: It plays a crucial role in developing new pharmaceuticals, particularly in creating peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Protein Engineering: Researchers leverage its properties to modify proteins, improving their stability and functionality for various applications in biotechnology.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, aiding in the understanding of signaling pathways and potential treatments for neurological disorders.

Citations