CAS 146982-27-6
:N(alpha)-fmoc-N(epsilon)-alloc-L-lysine
Description:
N(alpha)-Fmoc-N(epsilon)-alloc-L-lysine is a derivative of the amino acid lysine, modified to enhance its utility in peptide synthesis and other biochemical applications. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino terminus, allowing for selective reactions without interfering with the lysine's reactivity. The "alloc" (allyloxycarbonyl) group protects the epsilon amino group, providing a means for subsequent deprotection and functionalization. This compound is typically used in solid-phase peptide synthesis, where the protection of functional groups is crucial for the stepwise assembly of peptides. Its structure allows for the introduction of various side chains and modifications, making it versatile in the design of peptides with specific properties. The presence of both Fmoc and alloc groups enables chemists to manipulate the molecule's reactivity and stability under different conditions. Overall, N(alpha)-Fmoc-N(epsilon)-alloc-L-lysine is a valuable building block in the field of peptide chemistry, facilitating the synthesis of complex peptides and proteins.
Formula:C25H28N2O6
InChI:InChI=1/C25H28N2O6/c1-2-15-32-24(30)26-14-8-7-13-22(23(28)29)27-25(31)33-16-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-6,9-12,21-22H,1,7-8,13-16H2,(H,26,30)(H,27,31)(H,28,29)/t22-/m0/s1
SMILES:C=CCOC(=NCCCC[C@@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12)O
Synonyms:- Fmoc-Lys(Aloc)-OH
- Fmoc-Lys(Alloc)-OH
- N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]-N~6~-[(prop-2-en-1-yloxy)carbonyl]-L-lysine
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Found 9 products.
N6-[(Allyloxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine
CAS:Formula:C25H28N2O6Purity:>96.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:452.51Nε-Allyloxycarbonyl-Nα-Fmoc-L-lysine, 95%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C25H28N2O6Purity:95%Molecular weight:452.51Fmoc-Lys(Aloc)-OH
CAS:The selectively cleavable Alloc group allows on-resin modification of lysine side-chains during Fmoc-SPPS.Formula:C25H28N2O6Purity:98.7%Color and Shape:WhiteMolecular weight:452.51N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-L-lysine
CAS:Formula:C25H28N2O6Purity:97%Color and Shape:SolidMolecular weight:452.4996Fmoc-Lys(Alloc)-OH
CAS:<p>Fmoc-Lys(Alloc)-OH is a lysine derivative containing Fmoc protecting group, which can be used for peptide synthesis and drug design.</p>Formula:C25H28N2O6Purity:98.49%Color and Shape:SolidMolecular weight:452.5Fmoc-Lys(Alloc)-OH
CAS:Formula:C25H28N2O6Purity:≥ 98.0%Color and Shape:White powder or crystalsMolecular weight:452.50Fmoc-Lys(Alloc)-OH
CAS:<p>M06250 - Fmoc-Lys(Alloc)-OH</p>Formula:C25H28N2O6Purity:97%Color and Shape:Solid, Beige powderMolecular weight:452.507Fmoc-L-Lys(Alloc)-OH
CAS:<p>Fmoc-L-Lys(Alloc)-OH is a peptide that consists of an amino acid sequence that is a variant of the human insulin molecule. The peptide has been modified to incorporate a pegyl group, which increases the serum stability of this drug and prevents enzymatic degradation. This compound has been tested in vitro by binding to nuclear DNA and inhibiting receptor binding. Fmoc-L-Lys(Alloc)-OH has also shown anticancer effects in vivo with tumor xenografts and apoptosis protein expression in human serum, as well as an increase in serine protease activity.</p>Formula:C25H28N2O6Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:452.5 g/mol









