The compound (3- {5- [(2, 5-dimethoxyphenyl) amino]-1,3,4-thiadiazolidin-2-yl}-5,8-methoxy-2H-chromen-2-one) inhibits the prion protein conversion from PrPC to PrPSc with lower IC50 in ScN2a cells

Publication date: Available online 19 September 2017
Source:Bioorganic & Medicinal Chemistry
Author(s): Nataraj S. Pagadala, Trent C. Bjorndahl, Michael Joyce, David S. Wishart, Khajamohiddin Syed, Abdolamir Landi
Prion diseases are fatal neurodegenerative disorders of the central nervous system characterized by the accumulation of a protease resistant form (PrP^Sc) of the cellular prion protein (PrP^C) in the brain. Two types of cellular prion (PrP^C) compounds have been identified that appear to affect prion conversion are known as Effective Binders (EBs) and Accelerators (ACCs). Effective binders shift the balance in favour of PrP^C, whereas Accelerators favour the formation of PrP^Sc. Molecular docking indicates EBs and ACCs both bind to pocket-D of the SHaPrP^C molecule. However, EBs and ACCs may have opposing effects on the stability of the salt bridge between Arg¹⁵⁶ and Glu¹⁹⁶/Glu²⁰⁰. Computational docking data indicate that the hydrophobic benzamide group of the EB, GFP23 and the 1-(3, 3-dimethylcyclohexylidene) piperidinium group of the ACC, GFP22 play an important role in inhibition and conversion from SHaPrP^C to SHaPrP^Sc, respectively. Experimentally, NMR confirmed the amide chemical shift perturbations observed upon the binding of GFP23 to pocket-D of SHaPrP^C. Consistent with its role as an ACC, titration of GFP22 resulted in widespread chemical shift changes and signal intensity loss due to protein unfolding. Virtual screening of a ligand database using the molecular scaffold developed from the set of EBs identified six of our compounds (previously studied using fluorescence quenching) as being among the top 100 best binders. Among them, compounds 5 and 6 were found to be particularly potent in decreasing the accumulation SHaPrP^Sc in ScN2a cells with an IC50 of ∼35 µM and 20 µM.

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