Search Results - "Hilbers, Hans W"

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    Cyclotriveratrylene (CTV) as a New Chiral Triacid Scaffold Capable of Inducing Triple Helix Formation of Collagen Peptides Containing either a Native Sequence or Pro-Hyp-Gly Repeats by Rump, Erik T., Rijkers, Dirk T. S., Hilbers, Hans W., de Groot, Philip G., Liskamp, Rob M. J.

    Published in Chemistry : a European journal (18-10-2002)
    “…A new triacid scaffold is described based on the cone‐shaped cyclotriveratrylene (CTV) molecule that facilitates the triple helical folding of peptides…”
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    Step-wise and pre-organization induced synthesis of a crossed alkene-bridged nisin Z DE-ring mimic by ring-closing metathesis by Ghalit, Nourdin, Kemmink, Johan, Hilbers, Hans W, Versluis, Cees, Rijkers, Dirk T S, Liskamp, Rob M J

    Published in Organic & biomolecular chemistry (01-01-2007)
    “…This paper describes two approaches for the synthesis of a crossed alkene-bridged mimic of the thioether ring system of the nisin Z DE-fragment. The first…”
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    Ring-closing metathesis for the synthesis of side chain knotted pentapeptides inspired by vancomycin by ten Brink, Hefziba T, Rijkers, Dirk T S, Kemmink, Johan, Hilbers, Hans W, Liskamp, Rob M J

    Published in Organic & biomolecular chemistry (21-09-2004)
    “…A versatile method for the synthesis of bicyclic side chain knotted peptides inspired by vancomycin is described. The synthetic approach is based on the…”
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    Role of solution conformation and flexibility of short peptide ligands that bind to the p56(lck) SH2 domain by Dekker, Frank J, de Mol, Nico J, Bultinck, Patrick, Kemmink, Johan, Hilbers, Hans W, Liskamp, Rob M J

    Published in Bioorganic & medicinal chemistry (20-03-2003)
    “…A general approach in drug design is making ligands more rigid in order to avoid loss in conformational entropy (deltaS(conf)) upon receptor binding. We…”
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  7. 7

    Generate: A program for 3-D structure generation and conformational analysis of peptides and peptidomimetics by Bultinck, Patrick, Augustynen, Stijn, Hilbers, Hans W., Moret, Ed E., Tollenaere, Jan P.

    Published in Journal of computational chemistry (01-05-2002)
    “…The program Generate, aimed at generating 3‐D structures for peptides and peptidomimetics, is presented. The algorithm is based on a build‐up procedure, using…”
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    In Vivo Activity and Hydrophobicity of Cytostatic Aziridinyl Quinones by Moret, Ed E, de Boer, Mark, Hilbers, Hans W, Tollenaere, Jan P, Janssen, Lambert H. M, Holthuis, Joost J. M, Driebergen, Reinoud J, Verboom, Willem, Reinhoudt, David N

    Published in Journal of medicinal chemistry (02-02-1996)
    “…For a series of 3,6-disubstituted bisaziridinylbenzoquinones the in vivo and in vitro activities against murine tumors, as well as the in vivo toxicity, are…”
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    Synthesis and biological evaluation of potent α vβ 3-integrin receptor antagonists by Dijkgraaf, Ingrid, Kruijtzer, John A.W., Frielink, Cathelijne, Soede, Annemieke C., Hilbers, Hans W., Oyen, Wim J.G., Corstens, Frans H.M., Liskamp, Rob M.J., Boerman, Otto C.

    Published in Nuclear medicine and biology (2006)
    “…α vβ 3 Integrin is expressed in sprouting endothelial cells in growing tumors, whereas it is absent in quiescent blood vessels. In addition, various tumor cell…”
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    Synthesis and biological evaluation of potent alphavbeta3-integrin receptor antagonists by Dijkgraaf, Ingrid, Kruijtzer, John A W, Frielink, Cathelijne, Soede, Annemieke C, Hilbers, Hans W, Oyen, Wim J G, Corstens, Frans H M, Liskamp, Rob M J, Boerman, Otto C

    Published in Nuclear medicine and biology (01-11-2006)
    “…alpha(v)beta(3) Integrin is expressed in sprouting endothelial cells in growing tumors, whereas it is absent in quiescent blood vessels. In addition, various…”
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    Journal Article
  12. 12

    Role of solution conformation and flexibility of short peptide ligands that bind to the p56 lck SH2 domain by Dekker, Frank J, de Mol, Nico J, Bultinck, Patrick, Kemmink, Johan, Hilbers, Hans W, Liskamp, Rob M.J

    Published in Bioorganic & medicinal chemistry (2003)
    “…A general approach in drug design is making ligands more rigid in order to avoid loss in conformational entropy (Δ S conf) upon receptor binding. We…”
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    Journal Article
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