Boc-L-Ser(Propargyl)-OH*DCHA

Chemical name: N-alpha-t-Butyloxycarbonyl-O-propargyl-L-serine dicyclohexylamine // Synonyms: Boc-Ser(Propargyl)-OH*DCHA, Boc-Ser(Propargyl)-OH*DCHA

  • Product code:BAA2260
  • CAS No.:145205-94-3 (net)
  • Formula:C11H17NO5*C12H23N
  • Storage temperature:2-8°C
  • Molecular weight:243.26*181.32 g/mol

from €200.00

Grouped product items
Qty Packing unit Price SKU Availability
1 g
€200.00
BAA2260.0001
<10 business days
5 g
€700.00
BAA2260.0005
<10 business days
25 g
€2,700.00
BAA2260.0025
>20 business days
references

'Click' glycosylation of peptides through cysteine propargylation and CuAAC; S. Lamande-Langle, C. Collet, R. Hensienne, C. Vala, F. Chretien, Y. Chapleur, A. Mohamadi, P. Lacolley and V. Regnault; Bioorg Med Chem 2014; 22: 6672-6683. https://doi.org/10.1016/j.bmc.2014.09.056

Photoinduced addition of glycosyl thiols to alkynyl peptides: use of free-radical thiol-yne coupling for post-translational double-glycosylation of peptides; M. Lo Conte, S. Pacifico, A. Chambery, A. Marra and A. Dondoni; J Org Chem 2010; 75: 4644-7. https://doi.org/10.1021/jo1008178

Lacosamide isothiocyanate-based agents: novel agents to target and identify lacosamide receptors; K. D. Park, P. Morieux, C. Salome, S. W. Cotten, O. Reamtong, C. Eyers, S. J. Gaskell, J. P. Stables, R. Liu and H. Kohn; Journal of medicinal chemistry 2009; 52: 6897-911. https://doi.org/10.1021/jm9012054

On the function and structure of synthetically modified porins; S. Reitz, M. Cebi, P. Reiss, G. Studnik, U. Linne, U. Koert and L. O. Essen; Angew Chem Int Ed Engl 2009; 48: 4853-7. https://doi.org/10.1002/anie.200900457

Non-enzymatic covalent protein labeling using a reactive tag; H. Nonaka, S. Tsukiji, A. Ojida and I. Hamachi; J Am Chem Soc 2007; 129: 15777-9. https://doi.org/10.1021/ja074176d

Isoxazolyl-serine-based agonists of peroxisome proliferator-activated receptor: design, synthesis, and effects on cardiomyocyte differentiation; Z. L. Wei, P. A. Petukhov, F. Bizik, J. C. Teixeira, M. Mercola, E. A. Volpe, R. I. Glazer, T. M. Willson and A. P. Kozikowski; J Am Chem Soc 2004; 126: 16714-5. https://doi.org/10.1021/ja046386l


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