Fmoc-L-Lys(Pryoc)-OH

Nombre químico: (S)-2-((9-Fluorenylmethyloxyl)amino)-6-((prop-2-ynyloxy)carbonylamino)hexanoic acid // Sinónimos: N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-epsilon-(prop-2-ynyloxycarbonyl)-L-lysine, Fmoc-Lys(Pryoc)-OH, Fmoc-Lys(Proc)-OH, Fmoc-Lys(Pryoc)-OH

  • Nº Artículo:FAA3150
  • Nº CAS:1584133-25-4
  • Fórmula:C25H26N2O6
  • Storage temperature:2-8°C
  • Masa molecular:450,48 g/mol
  • Pureza:min. 98%
  • Pureza Enantiomérica:min. 99,7%

from 108,00 €

Grouped product items
Cantidad Unidad de venta Precio Unidad de almacenamiento de stock (SKU) Disponibilidad
500 mg
108,00 €
FAA3150.0500
<10 días laborables
1 g
168,00 €
FAA3150.0001
<10 días laborables
5 g
600,00 €
FAA3150.0005
<10 días laborables
25 g
2.400,00 €
FAA3150.0025
<10 días laborables
description

tRNA can be loaded with the propargyl analogue of free L-lysine by pyrrolysyl-tRNA synthetase enabling the biochemist to introduce site specifically an alkyne group into a protein for further click conjugation.

Propargyloxycarbonyl, commonly abbreviated as Poc or Pryoc, can either be used as alkyne component for standard Click conjugation or in combination with tetrazine linkers in copper-free Diels-Alder type Click reactions. It also has applications as unusual protecting group for amines, hydroxy functions and as esters. All 3 are stable to neat TFA, but can be cleaved at ambient temperature with Co2(CO)8 in TFA:DCM. Deprotection with other transition metals like palladium have also been reported.

references

Bioorthogonal Catalysis: A General Method To Evaluate Metal-Catalyzed Reactions in Real Time in Living Systems Using a Cellular Luciferase Reporter System; H. T. Hsu, B. M. Trantow, R. M. Waymouth and P. A. Wender; Bioconjug Chem 2016; 27: 376-82. https://doi.org/10.1021/acs.bioconjchem.5b00469

N-alkynyl derivatives of 5-fluorouracil: susceptibility to palladium-mediated dealkylation and toxigenicity in cancer cell culture; J. T. Weiss, C. Fraser, B. Rubio-Ruiz, S. H. Myers, R. Crispin, J. C. Dawson, V. G. Brunton, E. E. Patton, N. O. Carragher and A. Unciti-Broceta; Front Chem 2014; 2: 56. https://doi.org/10.3389/fchem.2014.00056

Palladium-triggered deprotection chemistry for protein activation in living cells; J. Li, J. Yu, J. Zhao, J. Wang, S. Zheng, S. Lin, L. Chen, M. Yang, S. Jia, X. Zhang and P. R. Chen; Nat Chem 2014; 6: 352-61. https://doi.org/10.1038/nchem.1887

Genetic encoding and labeling of aliphatic azides and alkynes in recombinant proteins via a pyrrolysyl-tRNA Synthetase/tRNA(CUA) pair and click chemistry; D. P. Nguyen, H. Lusic, H. Neumann, P. B. Kapadnis, A. Deiters and J. W. Chin; J Am Chem Soc 2009; 131: 8720-1. https://doi.org/10.1021/ja900553w

Direct charging of tRNACUA with pyrrolysine in vitro and in vivo; S. K. Blight, R. C. Larue, A. Mahapatra, D. G. Longstaff, E. Chang, G. Zhao, P. T. Kang, K. B. Green-Church, M. K. Chan and J. A. Krzycki; Nature 2004; 431: 333. https://doi.org/10.1038/nature02895

Propargyloxycarbonyl and propargyl groups for novel protection of amino, hydroxy, and carboxy functions; Y. Fukase, K. Fukase and S. Kusumoto; Tetrahedron Letters 1999; 40: 1169-1170. https://doi.org/10.1016/s0040-4039(98)02555-6


* Disclaimer
We refer to our general terms and conditions.
All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.

¿Necesita más información sobre este producto?

ponerse en contacto

Contacto rápido

Por favor envíeme más información sobre

¡Otros productos que también podrían interesarle!