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Thank you very much for your interest in our products. All prices listed on our website are ex-works, Germany, and may attract customs duties when imported.
You may/will be contacted by the shipping company for additional documentation that may be required by the US Customs for clearance.
We offer you the convenience of buying through a local partner, Peptide Solutions LLC who can import the shipment as well as prepay the customs duties and brokerage on your behalf and provide the convenience of a domestic sale.
Continue to Iris Biotech GmbHSend request to US distributorChemical name: N-alpha-(9-fluorenylmethyloxycarbonyl)-N-epsilon-acetyl-L-lysine // Synonyms: N-epsilon-acetyl-N-alpha-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine, (2S)-6-Acetamido-2-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)hexanoic acid,N-alpha-Fmoc-N-epsilon-acetyl-L-lysine, Fmoc-Lys(Ac) -OH, Fmoc-Lys(COCH3), Fmoc-Lys(Ac), Fmoc-L-AcK, Fm
from €150.00
Lipidated amino acids have raised interest as they are reported to improve the pharmacokinetic and pharmacologic properties of peptide APIs and other biopharmaceuticals. This acetylated Lysine represents a short “fatty” amino acid derivative suitable for activity studies.
Furthermore, the acetylation of lysine is a common posttranslational modification with many regulatory roles. As an example, the modification of histone proteins and the interaction of acetylated lysines with aromatic rings is commonly observed in transcriptionally relevant protein-protein interactions. Thus, this acetylated lysine can be used to study protein structure, interactions, and activity.
Effects of Lysine Acetylation in a b-Hairpin Peptide: Comparison of an Amide-ð and a Cation-ð Interaction; R. M. Hughes, L. M. Waters; J. Am. Chem. Soc. 2006; 128(41): 13586-13591. https://doi.org/10.1021/ja0648460.
Substrate specificity of SIRT1-catalyzed lysine Nepsilon-deacetylation reaction probed with the side chain modified Nepsilon-acetyl-lysine analogs; Bioorg. Chem. 2010; 38(1): 17-25. https://doi.org/10.1016/j.bioorg.2009.10.001.
Mechanistic studies of malonic acid-mediated in situ acylation; K. Chandra, J. N. Naoum, T. K. Roy, C. Gilon, R. B. Gerber, A. Friedler; Biopolymers 2015; 104(5): 495-505. https://doi.org/10.1002/bip.22654.
Effect of lysine methylation and acetylation on the RNA recognition and cellular uptake of Tat-derived peptides; M.-C. Liu, C.-Y. Chen, C.-H. Chiang; W.-M. Wang, R. P. Cheng; Bioorg. Med. Chem. 2016; 24(21): 5047-5051. https://doi.org/10.1016/j.bmc.2016.08.015.
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