Publication | Open Access
<i>C</i><sub>2</sub>‐Symmetrical Thiodigalactoside Bis‐Benzamido Derivatives as High‐Affinity Inhibitors of Galectin‐3: Efficient Lectin Inhibition through Double Arginine–Arene Interactions
129
Citations
14
References
2005
Year
Dissociation ConstantDouble Arginine–arenePeptide ScienceChemical BiologyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryEfficient Lectin InhibitionHigh‐affinity InhibitorsAnti-cancer AgentInhibitory ActivityBiochemistryAromatic Amide SubstituentsMechanism Of ActionPharmacologyMolecular ModelingNatural SciencesDrug DiscoveryRational Drug DesignMedicineSmall MoleculesDouble Arginine–arene Interactions
Inhibitors of galectin-3, which has been implicated in cancer- and immunity-related processes, can be synthesized from thiodigalactoside derivatives with aromatic amide substituents at both C3 positions (see structure). Dissociation constant (Kd) values as low as 33 nM have been obtained. Computer modeling suggests that such high affinity stems from double arginine–arene stacking interactions. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2005/z500627_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
| Year | Citations | |
|---|---|---|
Page 1
Page 1