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Catalog Number:
28557
CAS Number:
194718-17-7
( S )- N -α-Fmoc-N'-Boc-homolisina
Purity:
≥ 97,1 % (HPLC)
Synonym(s):
Fmoc-L-Holys(Boc)-OH, Ácido ( S )-Fmoc-2-amino-7-(Boc-amino)-heptanoico
Documents
$188.28 /25 mg
Tamaño
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Product Information

(S)-N-a-Fmoc-N'-Boc-homo-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique combination of protective groups, specifically the Fmoc (fluorenylmethyloxycarbonyl) and Boc (tert-butyloxycarbonyl) moieties, which facilitate the selective functionalization of amino acids during solid-phase peptide synthesis. Its structural properties make it an excellent choice for researchers looking to create complex peptides with enhanced stability and solubility.

In practical applications, (S)-N-a-Fmoc-N'-Boc-homo-lysine is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions. Its ability to serve as a building block for modified peptides allows for the exploration of new biological activities and therapeutic potentials. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in generating high-purity products, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-L-Holys(Boc)-OH, Ácido ( S )-Fmoc-2-amino-7-(Boc-amino)-heptanoico
CAS Number
194718-17-7
Purity
≥ 97,1 % (HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.57
MDL Number
MFCD01860606
PubChem ID
56845672
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = 18,4 ± 1 º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Holys(Boc)-OH, Ácido ( S )-Fmoc-2-amino-7-(Boc-amino)-heptanoico
CAS Number
194718-17-7
Purity
≥ 97,1 % (HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.57
MDL Number
MFCD01860606
PubChem ID
56845672
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = 18,4 ± 1 º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-N-a-Fmoc-N'-Boc-homo-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide sequences with high purity.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, offering a way to modify peptide structures for enhanced stability and bioactivity, which is essential in pharmaceutical research.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of peptides to other biomolecules, such as antibodies or drugs, facilitating targeted delivery in medical applications.
  • Protein Engineering: Researchers utilize it in protein engineering to introduce homo-lysine residues into proteins, which can improve their properties, such as solubility and stability, making them more effective in various applications.
  • Research in Immunology: This compound is valuable in immunology studies, where modified peptides can be used to understand immune responses and develop vaccines, providing insights into disease mechanisms.

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