PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Czasopismo
2012 | 10 | 1 | 113-120
Tytuł artykułu

Synthesis and properties of new biotin compounds containing hexyltriethylene glycol chain

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The synthesis of a new halogenide containing hexyltriethylene glycol chain functionalized with biotin is reported. The general possibility of this linker to use as the building block for biotinylated compounds syntheses is demonstrated. Two biotinylated esters with different properties for useful surface modification and as fluorescence probes for proteins marking were synthesized. The properties of mentioned compounds were investigated by using surface plazmon resonance ellypsometry and fluorescence spectroscopy.
Wydawca

Czasopismo
Rocznik
Tom
10
Numer
1
Strony
113-120
Opis fizyczny
Daty
wydano
2012-02-01
online
2011-11-24
Twórcy
  • Institute of Chemistry of Center for Physical Sciences and Technology
  • Vilnius University
  • Institute of Chemistry of Center for Physical Sciences and Technology
  • Vilnius University
  • Institute of Chemistry of Center for Physical Sciences and Technology, lorka@ktl.mii.lt
Bibliografia
  • [1] D. Chen, J. Li, Surf. Sci. Reports 61, 445 (2006) http://dx.doi.org/10.1016/j.surfrep.2006.08.001[Crossref]
  • [2] F. Schreiber, Prog. Surf. Sci. 65, 151 (2000) http://dx.doi.org/10.1016/S0079-6816(00)00024-1[Crossref]
  • [3] J. Noh, M. Hara, RIKEN Review 38, 49 (2001)
  • [4] A.B. Sieval, R. Linke, H. Zuilhof, E.J.R. Sudhölter, Adv. Mater. 12(19), 1457 (2000)
  • [5] H.-Y. Nie, N.S. McIntyre, W.M. Lau, J.M. Feng, Thin Solid Films 517, 814 (2008) http://dx.doi.org/10.1016/j.tsf.2008.09.021[Crossref]
  • [6] J.J. Gooding, F. Mearns, W. Yang, J. Liu, Electroanal. 15(2), 81 (2003) http://dx.doi.org/10.1002/elan.200390017[Crossref]
  • [7] N.K. Chaki, K. Vijayamohanan, Biosens. Bioelectron. 17, 1 (2002) http://dx.doi.org/10.1016/S0956-5663(01)00277-9[Crossref]
  • [8] J.H. Fendler, Chem. Mater. 13, 3196 (2001) http://dx.doi.org/10.1021/cm010165m[Crossref]
  • [9] M. Aslam, N.K. Chaki, J. Sharma, K. Vijayamohanan, Curr. Appl. Phys. 3, 115 (2003) http://dx.doi.org/10.1016/S1567-1739(02)00180-3[Crossref]
  • [10] J. Xu, J. Xia, Z. Lin, Angew. Chem. Int. Ed. 46, 1860 (2007) http://dx.doi.org/10.1002/anie.200604540[Crossref]
  • [11] L. Wang, A. Rastelli, S. Kiravittaya, R. Songmuang, O.G. Schmidt, B. Krause, T.H. Metzger, Nanoscale Res. Lett. 1, 74 (2006) http://dx.doi.org/10.1007/s11671-006-9003-y[Crossref]
  • [12] Y.-H.M. Chan, S.G. Boxer, Curr. Opin. Chem. Biol. 11, 1 (2007) http://dx.doi.org/10.1016/j.cbpa.2007.09.020[Crossref]
  • [13] W. Knoll, I. Köper, R. Naumann, E.-K. Sinner, Electrochim. Acta 53, 6680 (2008) http://dx.doi.org/10.1016/j.electacta.2008.02.121[Crossref]
  • [14] I. Köper, Mol. BioSyst. 3, 651 (2007) http://dx.doi.org/10.1039/b707168j[Crossref]
  • [15] W. Huang, M. Helvenston, Langmuir 15, 6510 (1999) http://dx.doi.org/10.1021/la990237c[Crossref]
  • [16] A. Bajorek, K. Trzebiatowska, B. Jędrzejewska, M. Pietrzak, R. Gawinecki, J. Pączkowski, J. Fluoresc. 14(3), 295 (2004) http://dx.doi.org/10.1023/B:JOFL.0000024562.60225.d0[Crossref]
  • [17] M.F. Pepitone, G.G. Jernigan, J.S. Melinger, O.-K. Kim, Org. Lett. 9(5), 801 (2007) http://dx.doi.org/10.1021/ol063000y[Crossref]
  • [18] P.G. Lacroix, J.C. Daran, Chem. Mater. 10, 1109 (1998) http://dx.doi.org/10.1021/cm970692z[Crossref]
  • [19] B. Rudat, E. Birtalan, I. Thomé, D.K. Kölmel, V.L. Horhoiu, M.D. Wissert, U. Lemmer, H.-J. Eisler, T.S. Balaban, S. Bräse, J. Phys. Chem. B 114, 13473 (2010) http://dx.doi.org/10.1021/jp103308s[Crossref]
  • [20] T. H. Nguyen Pham, R.J. Clarke, J. Phys. Chem. B, 112, 6513 (2008) http://dx.doi.org/10.1021/jp711694u[Crossref]
  • [21] D.N. Ng, P. Fromherz, ACS Chem. Biol. 6, 444 (2011) http://dx.doi.org/10.1021/cb100312d[Crossref]
  • [22] B. Kuhn, P. Fromherz, J. Phys. Chem. B, 107, 7903 (2003) http://dx.doi.org/10.1021/jp0345811[Crossref]
  • [23] E. Gizeli, M. Liley, C.R. Lowe, H. Vogel, Anal. Chem. 69, 4808 (1997) http://dx.doi.org/10.1021/ac970519m[Crossref]
  • [24] S. Hleli, C. Martelet, A. Abdelghani, N. Burais, N. Jaffrezic-Renault, Sensor. Actuator. B113, 711 (2006)
  • [25] P.A. Millner, H.C.W. Hays, A. Vakurov, N.A. Pchelintse, M.M. Billah, M.A. Rodger, Semin. Cell. Dev. Biol. 20, 34 (2009) http://dx.doi.org/10.1016/j.semcdb.2009.01.011[Crossref]
  • [26] J.M. Harris, S. Zalipsky (Eds.), Poly(ethylene glycol) Chemistry and Biological Applications (American Chemical Society, San Francisco, 1997)
  • [27] E. Prats-Alfonso, F. Garcia-Martin, N. Bayo, L.J. Cruz, M. Pla-Roca, J. Samitier, A. Errachid, F. Albericio, Tetrahedron 62, 6876 (2006) http://dx.doi.org/10.1016/j.tet.2006.04.090[Crossref]
  • [28] C.A. Canaria, J.O. Smith, C.J. Yu, S.E. Fraser, R. Lansford, Tetrahedron Lett. 46, 4813 (2005) http://dx.doi.org/10.1016/j.tetlet.2005.04.091[Crossref]
  • [29] D. Witt, R. Klajn, P. Barski, B.A. Grzybowski, Curr. Org. Chem. 8, 1763 (2004) http://dx.doi.org/10.2174/1385272043369421[Crossref]
  • [30] T.M. Hansen, M.M. Engler, C.J. Fortsyth, Bioorg. Med. Chem. Lett. 13, 2127 (2003) http://dx.doi.org/10.1016/S0960-894X(03)00355-X[Crossref]
  • [31] M. Kažemėkaitė, A. Bulovas, V. Smirnovas, G. Niaura, E. Butkus, V. Razumas, Tetrahedron Lett. 42, 7691 (2001) http://dx.doi.org/10.1016/S0040-4039(01)01625-2[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-011-0113-8
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.