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Targeting cancer cells with folic acid–iminoboronate fluorescent conjugates†
Pedro M. S. D. Cal,Raquel F. M. Frade,Vijay Chudasama,Carlos Cordeiro,Stephen Caddick,Pedro M. P. Gois
Chemical Communications Pub Date : 11/05/2013 00:00:00 , DOI:10.1039/C3CC47534D
Abstract

Herein we present the synthesis of fluorescent 2-acetylbenzeneboronic acids that undergo B–N promoted conjugation with lysozyme and N-(2-aminoethyl) folic acid (EDA-FA), generating conjugates that are selectively recognized and internalized by cancer cells that over-express folic acid receptors.

Graphical abstract: Targeting cancer cells with folic acid–iminoboronate fluorescent conjugates
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