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Updated: Aug 19, 2026

Genetically-encoded Molecular Probes to Study G Protein-coupled Receptors
Published on: September 13, 2013
Synthesis and biological study of a flavone acetic acid analogue containing an azido reporting group designed as a
Krishnan Malolanarasimhan1, Christopher C Lai, James A Kelley
1Laboratory of Medicinal Chemistry, Center for Cancer Research, National Cancer Institute-Frederick, Center for Cancer Research, Frederick, MD 21702-1201, USA.
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.
