Title of article :
Synthesis and biological study of a flavone acetic acid analogue containing an azido reporting group designed as a multifunctional binding site probe Original Research Article
Author/Authors :
Krishnan Malolanarasimhan، نويسنده , , Christopher C. Lai، نويسنده , , James A. Kelley، نويسنده , , Lynn Iaccarino، نويسنده , , Della Reynolds، نويسنده , , Howard A. Young، نويسنده , , Victor E. Marquez، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Abstract :
Flavone-8-acetic acid (FAA) is a potent immunomodulatory small molecule that is uniquely characterized as being active on mouse but not human cells. Although FAA is a potent inducer of murine cytokine, chemokine and interferon gene expression, its mode of action remains unknown. In this report, we describe the synthesis of a new flavone acetic acid (FAA) analogue, (2-[2-(4-azidophenyl)-4-oxochromen-8-yl-]acetic acid (compound 2). We demonstrate that compound 2 is equally active as the parent FAA in inducing chemokine gene expression and that the azide functional group is capable of reacting with a reporter molecule, such as the FLAG peptide–phosphine, under mild conditions. This reaction will be useful for detecting the drug-bound protein active complex utilizing an anti-FLAG antibody.
Keywords :
Staudinger reaction , Immunomodulatory small molecules , Flavone acetic acid , Azide-modified flavone acetic acid , affinity label
Journal title :
Bioorganic and Medicinal Chemistry
Journal title :
Bioorganic and Medicinal Chemistry