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Pascal De Tullio

Researcher at University of Liège

Publications -  128
Citations -  2442

Pascal De Tullio is an academic researcher from University of Liège. The author has contributed to research in topics: Benzothiadiazine & AMPA receptor. The author has an hindex of 26, co-authored 122 publications receiving 2106 citations. Previous affiliations of Pascal De Tullio include Université libre de Bruxelles.

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Journal Article

New trends in the design of drugs against Alzheimer's disease

TL;DR: This review presents an overview of the several strategies and new classes of compounds against AD and indicates some of these innovative approaches tend to delay onset of AD, while others are still symptomatic.
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3-Alkylamino-4H-1,2,4-benzothiadiazine 1,1-Dioxides as ATP-Sensitive Potassium Channel Openers: Effect of 6,7-Disubstitution on Potency and Tissue Selectivity

TL;DR: Radioisotopic and fluorimetric experiments performed with the most potent compound inhibiting insulin release (34, BPDZ 259, 6-chloro-7-fluoro-3-isopropylamino-4H-1,2,4-benzothiadiazine 1,1-dioxide) confirmed that the drug activated K(ATP) channels.
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Design, synthesis, and pharmacological evaluation of R/S-3,4-dihydro-2,2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: toward tissue-selective pancreatic beta-cell KATP channel openers structurally related to (+/-)-cromakalim.

TL;DR: Radioisotopic and electrophysiological investigations performed with R/S-6-chloro-4-(3-chlorophenylaminocarbonylamino)-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran confirmed that the drug activated pancreatic KATP channels.
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Quality Assessment of Polygonum cuspidatum and Polygonum multiflorum by 1H NMR Metabolite Fingerprinting and Profiling Analysis.

TL;DR: An overview of the quality of P. cuspidatum and P. multiflorum samples available on the Chinese market is achieved and important metabolites for their discrimination are identified, using (1)H NMR-based metabolomics.
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Original 2-Alkylamino-6-halogenoquinazolin-4(3H)-ones and KATP Channel Activity

TL;DR: In conclusion, the newly synthesized quinazolinones interfere with insulin secretion and smooth muscle contractile activity and lack tissue selectivity.