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Search for "selectins" in Full Text gives 5 result(s) in Beilstein Journal of Organic Chemistry.

One-pot nucleophilic substitution–double click reactions of biazides leading to functionalized bis(1,2,3-triazole) derivatives

  • Hans-Ulrich Reissig and
  • Fei Yu

Beilstein J. Org. Chem. 2023, 19, 1399–1407, doi:10.3762/bjoc.19.101

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  • abstained from the conversion of compounds 24, 25 or 26 into their sulfated form due to the presence of the impurities in these samples. However, only the sulfated forms of this type of multivalent carbohydrate mimetics had earlier shown respectable biological activity as ligands of P- and L-selectins [44
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Published 18 Sep 2023

A systems-based framework to computationally describe putative transcription factors and signaling pathways regulating glycan biosynthesis

  • Theodore Groth,
  • Rudiyanto Gunawan and
  • Sriram Neelamegham

Beilstein J. Org. Chem. 2021, 17, 1712–1724, doi:10.3762/bjoc.17.119

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  • tumors. Sialyl Lewis-X is considered to be an important regulator of cancer metastasis as it binds the selectins on various vascular and blood cell types. Regulation of GalNAc-type O-linked glycans by SMAD2: SMAD2 was found to significantly affect core 1 and 2 O-linked glycan structures (enrichment p
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Published 22 Jul 2021

Synthesis of multivalent carbohydrate mimetics with aminopolyol end groups and their evaluation as L-selectin inhibitors

  • Joana Salta,
  • Jens Dernedde and
  • Hans-Ulrich Reissig

Beilstein J. Org. Chem. 2015, 11, 638–646, doi:10.3762/bjoc.11.72

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  • ; multivalency; selectins; sulfation; Introduction In a series of publications [1][2][3][4][5][6] our group reported on the syntheses of carbohydrate mimetics [7][8][9][10][11] that are based on aminopyrans, aminooxepanes or other aminopolyols. These compounds and their conjugates were prepared to be examined
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Published 05 May 2015

An easily accessible sulfated saccharide mimetic inhibits in vitro human tumor cell adhesion and angiogenesis of vascular endothelial cells

  • Grazia Marano,
  • Claas Gronewold,
  • Martin Frank,
  • Anette Merling,
  • Christian Kliem,
  • Sandra Sauer,
  • Manfred Wiessler,
  • Eva Frei and
  • Reinhard Schwartz-Albiez

Beilstein J. Org. Chem. 2012, 8, 787–803, doi:10.3762/bjoc.8.89

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  • ]. Furthermore, the overexpression of the charged blood group antigen sialyl Lewisx consisting of the terminal NeuNAcα2-3Galβ1-4(Fucα1-3)GlcNAc-group is correlated with carcinogenesis. It is recognized and bound by selectins, which are a subgroup of lectins that play an important role as cell-surface molecules
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Published 29 May 2012
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  • (particle diameter 6 nm). After sulfation of the hydroxyl groups the multivalent conjugates obtained displayed strong binding to P- and L-selectins, thus demonstrating that compounds such as 24 and 28 are of interest for the development of new anti-inflammatory agents [27][28]. Inspired by these first
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Published 09 Jul 2010
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