Molecular structure of Fmoc-Lys(Boc)-OH, CAS Number: 71989-26-9
Fmoc-Lys(Boc)-OH (CAS 71989-26-9)
Alternate Names:
Nα-Fmoc-Nε-Boc-L-lysine
Application:
Fmoc-Lys(Boc)-OH is a useful Fmoc and Boc protected Lysine for proteomics research
CAS Number:
71989-26-9
Molecular Weight:
468.54
Molecular Formula:
C26H32N2O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Fmoc-Lys(Boc)-OH is a useful Fmoc and Boc protected Lysine for proteomics research. It is a derivative of the naturally occurring amino acid lysine, and plays a pivotal role in peptide synthesis. Consequently, it has found application in the investigation of the biochemical impacts associated with peptides.
Fmoc-Lys(Boc)-OH (CAS 71989-26-9) References
- Chiral separation by simultaneous use of vancomycin as stationary phase chiral selector and chiral mobile phase additive. | Sun, Q. and Olesik, SV. 2000. J Chromatogr B Biomed Sci Appl. 745: 159-66. PMID: 10997711
- Efficient acylation of the N-terminus of highly hindered C(alpha)(alpha)-disubstituted amino acids via amino acid symmetrical anhydrides. | Fu, Y. and Hammer, RP. 2002. Org Lett. 4: 237-40. PMID: 11796059
- DNA binding behavior of peptides carrying acridinyl units: First example of effective poly-intercalation. | Ueyama, H., et al. 2001. Nucleic Acids Res Suppl. 163-4. PMID: 12836315
- Novel synthesis of a tetra-acridinyl peptide as a new DNA polyintercalator. | Ueyama, H., et al. 2000. Nucleic Acids Symp Ser. 133-4. PMID: 12903304
- Bis-naphthalene diimide exhibiting an effective bis-threading intercalating ability. | Nojima, T., et al. 2003. Nucleic Acids Res Suppl. 123-4. PMID: 14510411
- Fluoreometric behavior of a novel bis-acridine orange bound to double stranded DNA. | Takenaka, S., et al. 2003. Nucleic Acids Res Suppl. 151-2. PMID: 14510425
- Conformational constraint in protein ligand design and the inconsistency of binding entropy. | Udugamasooriya, DG. and Spaller, MR. 2008. Biopolymers. 89: 653-67. PMID: 18335423
- DOTA-functionalized polylysine: a high number of DOTA chelates positively influences the biodistribution of enzymatic conjugated anti-tumor antibody chCE7agl. | Grünberg, J., et al. 2013. PLoS One. 8: e60350. PMID: 23565233
- Pitfalls in the synthesis of fluorescent methotrexate oligopeptide conjugates. | Sebestyén, M., et al. 2016. Amino Acids. 48: 2599-2604. PMID: 27357306
- Fluorescent Peptide Beacons for the Selective Ratiometric Detection of Heparin. | Maity, D. and Schmuck, C. 2016. Chemistry. 22: 13156-61. PMID: 27534383
- Synthesis and Preclinical Evaluation of a Novel FAPI-04 Dimer for Cancer Theranostics. | Zhong, X., et al. 2023. Mol Pharm. 20: 2402-2414. PMID: 37015025
- Inhibition of cruzipain visualized in a fluorescence quenched solid-phase inhibitor library assay. D-amino acid inhibitors for cruzipain, cathepsin B and cathepsin L. | Meldal, M., et al. 1998. J Pept Sci. 4: 83-91. PMID: 9620612
- Suppression of side-reactions during the attachment of FMOC-amino acids to hydroxymethyl polymers† | J. W. van Nispen, J. P. Polderdijk, H. M. Greven. 1985. 104: 99-100.
- Controlled aggregation properties of single amino acids modified with protecting groups | Bharti Koshti,‡a Vivekshinh Kshtriya,‡a Soumick Naskar,‡a Hanuman Narodea and Nidhi Gour *a . 2022. New J. Chem. 6: 4746-4755.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-Lys(Boc)-OH, 5 g | sc-235193 | 5 g | $21.00 | |||
Fmoc-Lys(Boc)-OH, 10 g | sc-235193A | 10 g | $52.00 |