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Catalog Number:
12769
CAS Number:
203854-47-1
Nβ-Fmoc-Nω-Boc-L-β-homolysine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-HomoLys(Boc)-OH, (S-7-(Boc-amino)-3-(Fmoc-amino)heptanoic acid
Temperature Sensitive
Documents
$72.31 /100MG
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Product Information

Nb-Fmoc-Nw-Boc-L-b-homolysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique combination of protective groups, including the Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) moieties, which facilitate selective reactions and enhance stability during synthesis. Its structural properties make it an excellent choice for researchers looking to create complex peptides with improved solubility and bioactivity.

In practical applications, Nb-Fmoc-Nw-Boc-L-b-homolysine is particularly valuable in the fields of medicinal chemistry and biochemistry, where it is utilized in the design of peptide-based therapeutics and in the study of protein interactions. Its ability to provide a stable platform for further modifications allows for the development of innovative drug candidates. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, making it a preferred choice for those aiming to streamline their synthesis processes while achieving high yields and purity.

Synonyms
Fmoc-L-β-HomoLys(Boc)-OH, (S-7-(Boc-amino)-3-(Fmoc-amino)heptanoic acid
CAS Number
203854-47-1
Purity
≥ 98% (HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.58
MDL Number
MFCD01863054
PubChem ID
5066072
Appearance
White to off-white solid
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-L-β-HomoLys(Boc)-OH, (S-7-(Boc-amino)-3-(Fmoc-amino)heptanoic acid
CAS Number
203854-47-1
Purity
≥ 98% (HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.58
MDL Number
MFCD01863054
PubChem ID
5066072
Appearance
White to off-white solid
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Nb-Fmoc-Nw-Boc-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 various biological studies.
  • Drug Development: It is used in the development of novel therapeutics, particularly in designing peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound facilitates bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in drug delivery systems.
  • Protein Engineering: Researchers employ this chemical in protein engineering to modify and enhance the properties of proteins, improving their stability and functionality.
  • Diagnostics: It plays a role in the creation of diagnostic tools, where peptides derived from this compound can be used for specific detection of diseases.

Citations