Fmoc-Lys(Boc)-OH (Highly Pure)
| Catalog number: | B2015472 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 500 mg |
| Molecular Weight or Concentration: | 468.54 |
| Supplied as: | Powder |
| Applications: | a molecular tool for various biochemical applications |
| Storage: | 2-8C |
| Keywords: | N-Fmoc-N-Boc-L-lysine |
| Grade: | Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity>18 M-cm) and are filtered through 0.22 um. |
References
- Zhong X, Guo J, Han X, Wu W, Yang R, Zhang J, Shao G. Synthesis and Preclinical Evaluation of a Novel FAPI-04 Dimer for Cancer Theranostics Mol Pharm. 2023 May 1;20(5):2402-2414.
- Sebestyn M, Kczn G, Hudecz F. Pitfalls in the synthesis of fluorescent methotrexate oligopeptide conjugates Amino Acids. 2016 Nov;48(11):2599-2604.
- Nojima T, Ohtsuka K, Nagamatsu T, Takenaka S. Bis-naphthalene diimide exhibiting an effective bis-threading intercalating ability Nucleic Acids Res Suppl. 2003;(3):123-4.
- Meldal M, Svendsen IB, Juliano L, Juliano MA, Nery ED, Scharfstein J. Inhibition of cruzipain visualized in a fluorescence quenched solid-phase inhibitor library assay. D-amino acid inhibitors for cruzipain, cathepsin B and cathepsin L J Pept Sci. 1998 Apr;4(2):83-91.
- Takenaka S, Sakakibara Y, Ueyama H, Nojima T. Fluoreometric behavior of a novel bis-acridine orange bound to double stranded DNA Nucleic Acids Res Suppl. 2003;(3):151-2.
- Ueyama H, Waki M, Takagi M, Takenaka S. Novel synthesis of a tetra-acridinyl peptide as a new DNA polyintercalator Nucleic Acids Symp Ser. 2000;(44):133-4.
- Ueyama H, Takagi M, Waki M, Takenaka S. DNA binding behavior of peptides carrying acridinyl units: First example of effective poly-intercalation Nucleic Acids Res Suppl. 2001;(1):163-4.
- Kielmas M, Kijewska M, Kluczyk A, Oficjalska J, Gobiewska B, Stefanowicz P, Szewczuk Z. Comparison of modification sites in glycated crystallin in vitro and in vivo Anal Bioanal Chem. 2015 Mar;407(9):2557-67.
- Bayndr S, Aydoan C, Denizli A. Preparation of chiral monoliths with new modulation of the monolith surface chemistry for the enantioseparation of chiral drugs by nano-liquid chromatography J Chromatogr A. 2024 Jan 4;1713:464573.








