Using this HTS assay we screened a diverse library of ~80,000 compounds at a final concentration of 16.7µM. The selection criteria for a positive hit were based on a mean signal threshold of ?50% inhibition of control TSH stimulation. The screening resulted in 450 positive hits giving a hit ratio of 0.56%. A secondary confirmation screen against TSH and forskolin - a post receptor activator of adenylyl cyclase – confirmed one TSHR-specific candidate antagonist molecule (named VA-K-14). This lead molecule had an IC50 of 12.3µM a nd a unique chemical structure. A parallel analysis for cell viability indicated that the lead inhibitor was non-cytotoxic at its effective concentrations.
In-silico docking studies performed using a TSHR transmembrane model showed the hydrophobic contact locations and the possible mode of inhibition of TSHR signaling. Furthermore, this molecule was capable of inhibiting TSHR stimulation by Graves’ disease patient sera and monoclonal stimulating TSHR antibodies.
In conclusion, we report the identification of a novel small molecule TSHR inhibitor which has the potential to be developed as a therapeutic antagonist for abrogation of TSHR signaling by TSHR autoantibodies in Graves’ disease.