Author/Authors :
Jundong Zhang، نويسنده , , Georgiana Rivers، نويسنده , , Yanyi Zhu، نويسنده , , W. Alan Jacobson، نويسنده , , James Peyers، نويسنده , , Gretchen Grundstrom، نويسنده , , Peter Burch، نويسنده , , Sohail Hussein، نويسنده , , Ariane Marolewski، نويسنده , , Walter Herlihy، نويسنده , , James Rusche، نويسنده ,
Abstract :
Chemical libraries based on four-component condensation (4CC) reactions of isocyanides were constructed to identify compounds capable of blocking heparin binding to vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). The reaction products in the synthesized libraries contain heparin mimetic functional groups such as carbohydrates, sulfonates, carboxylates, and hydroxy groups. These libraries have been screened for the inhibition of heparin binding to growth factors such as VEGF and bFGF. Single point screening at 5.0 μM of the 18,720 reaction products generated 26 candidates. The IC50s of these 26 compounds were determined using HPLC-purified products and 20 of the 26 showed significant inhibition of heparin binding to VEGF and/or bFGF. Eighteen of the 20 confirmed active compounds have a linear extended structure. Structures identified in this library revealed an initial relationship of structure and activity, thus providing direction for further investigation of this type of heparin mimetic libraries.