https://www.selleckchem.com/products/OSI-906.html
A series of glycoside-peptide conjugates were prepared by engineering at the N-terminus of the natural peptide gramicidin A. The conjugate containing galactose moiety formed a unimolecular transmembrane channel and mediated ion transport to induce apoptosis of cancer cells. More importantly, it exhibited liver cancer cell-targeting behavior due to the galactose-asialoglycoprotein receptor recognition.Using a model molecule, we show that it is possible to create molecules that show the required properties for use as elements in a molecul
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